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Author Topic: The Attack of the Killer Nanobacteria  (Read 6243 times)
Harconen
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« on: August 28, 2009, 12:02:12 AM »

The Attack of the Killer Nanobacteria


Tiny creatures so small that they've been overlooked by scientists may be slinking around your body right now - and they're probably up to no good.

By Scott Anderson


So, naturalists observe, a flea
Has smaller fleas that on him prey;
And these have smaller still to bite 'em;
And so proceed ad infinitum.

-- Jonathan Swift


Bacterial Club Med? Could this steaming rainbow of heat-loving bacteria be the wellspring of life -- and the source of some nasty ailments?

In the 1970s, while doing field work in his beloved Italy, a geologist named Dr. Robert Folk from the University of Texas discovered that bacteria seemed to be precipitating - excreting, really - an unusual type of limestone. Known as travertine, it's been used for thousands of years in statuary and buildings all around the world, from the Coliseum in Rome to the Lincoln Center in New York. Why study travertine? As Dr. Folk puts it, "I was simply looking for a good excuse to continue doing field work in Italy because I loved the food and lifestyle, and hit upon the idea of working on the travertines of Rome."

Dr. Folk wasn't the first to notice that travertines are related to bacteria. These rocks are formed in steaming sulfurous cauldrons like those in Yellowstone, and it has been known for some time that so-called thermophilic bacteria actually thrive in the boiling, mineral-laden water. They create mats that geologists have always assumed would trap minerals and, over time, become fossilized. But Dr. Folk saw it differently. Rather than idle bystanders simply covered by sediment, he realized that the bacteria were actively creating calcium carbonate causing it to grow at rates far faster than seemed possible with ordinary chemistry.

A decade later, Dr. Folk and his colleagues, Leo Lynch and Brenda Kirkland, got access to a high-power electron microscope and had a chance to review some of his samples closer up. What they saw made them squint in disbelief. Organic-looking clumps of nodules were scattered all over the samples, far smaller than ordinary bacteria but with many similar shapes. When he asked around, he found that these had been noted before by other researchers, but they were assumed to be artifacts, perhaps caused by the preparation of the sample.

But Folk had seen bacteria in rocks before, so he was less inclined to shrug off these tiny spheres as mere artifacts. And the more rocks he looked at, the more of the little spheres he found. After some research in the unfamiliar turf of bacteriology, he found a few references to ultramicrobacteria, and felt he had found the answer. He was ready to tell the world.

The Sound of One Hand Clapping

"The important role of nannobacteria in the mineralogical world was
discovered through dumb luck, idle curiosity and random reading."

-- Dr. Robert L. Folk


Chains of nanobacteria grow across a sample from the Bagnaccio hot springs in Viterbo, Italy. Inorganic processes rarely lead to chains, but bacteria do it all the time.
Credit: Lynch, Kirkland and Folk, University of Texas

The smallest living thing, as you undoubtedly learned in school, is the virus. It is so small that it doesn't even have enough genes to reproduce itself (making its claim to life rather tenuous). Instead, it depends on the kindness of strangers, mostly bacteria and higher-level cells, to do the copying for them.

So in 1992, when the feisty Dr. Folk announced that several kinds of rock seemed to be created by what looked like tiny bacteria not much bigger than a virus, he was greeted with a stony silence. He was ridiculed as a kook both out of his field and out of his depth.

Folk was claiming much more than a new Guinness Record for tiniest creature: he was proposing that these hitherto invisible life forms actually constituted the bulk of the world's biomass. As well as creating rocks, Dr. Folk said they were also responsible for breaking them down, creating dirt in the process. For good measure, Dr. Folk even blamed them for much of the metal corrosion in the world. These little creatures were just a few dozen nanometers (billionths of a meter) in size, so Dr. Folk dubbed them nanobacteria. Actually he used the prefix nanno, a variant favored by geologists, but most researchers have since adopted the shorter form.

Not everyone at the presentation laughed at Dr. Folk. Chris Romanek, a NASA scientist, thought about an interesting rock he had in his possession: a little chunk of Mars, in the form of a meteorite that had landed in Antarctica. When he looked at the meteorite under the same magnification Dr. Folk was using, he was amazed to see what looked like tiny 50-nanometer bacteria. They were connected in chains much like ordinary bacteria. When he checked for certain specific hydrocarbons associated with fossilized bacteria, he found a familiar signature. In addition, there were tiny magnetic particles found in the meteorite that were similar to the ones found inside many terrestrial bacteria. In 1996, Dave McKay of NASA went public with Romanek's work, suggesting that the Martian meteorite known as ALH84001 may show evidence of Martian life. The news captured headlines around the world.


NASA high-power electron microscope image of Martian meteorite. Does this look familiar?
Credit: NASA

Many skeptics remained to be convinced. NASA asked a panel of experts to render an opinion on the minimum size of life. Scientists at the 1999 NAS Workshop on Size Limits of Very Small Microorganisms agreed that a minimal living nanobe would require enough DNA for a core set of 250 proteins and at least one ribosome. A ribosome is a structure possessed by all known life forms; it acts like a workbench where proteins are hammered out according to the specs contained in the DNA. No ribosome, no proteins. All the DNA in the world won't help if you can't translate it into working proteins. As far as size is concerned, the ribosome is the kicker. It's at least 25 nanometers wide, all by itself. If you wadded up the core DNA along with the required ribosome, the tightest ball you can get would be about 200 nanometers in diameter. This might explain the largest of the nanobacteria, but it seemed to rule out the smaller ones, some of which are smaller than the ribosome alone.

That dampened the enthusiasm for nanobacteria somewhat. But hidden in that same workshop report was an another, more speculative, viewpoint: perhaps life could be smaller if it forsook DNA and used RNA instead.

A decade earlier, Sidney Altman and Thomas Cech had won the Nobel prize for demonstrating that RNA can have enzyme activity, meaning it can do some of the jobs previously considered the sole province of proteins. Cech even showed that RNA can reproduce itself without the aid of any other proteins. This amazing result led to speculation that life might have started out with a simple self-replicating polymer predating proteins by billions of years. This theory also seemed to imply that such RNA-based life must have been exterminated by Darwinian pressure with the advent of the "superior" DNA / protein scheme. After all, we haven't found any life forms based on self-replicating RNA, so they must have been wiped out, right? But what if that ancient life still exists in the world -- and still has the upper hand?

Meanwhile, Over in Finland.

At around the same time, at the University of Kuopio in Finland, Drs. Neva Ciftcioglu and Olavi Kajander were having a hell of a time with their cell cultures. Biologists the world round curse the lottery of the serum. It is not a minor complaint: a goodly percent of experiments with mammalian cells start out just fine only to succumb to some kind of infection along the way. Whatever it is, it kills the cells and ruins the experiment. There is nothing else to do but start over again, and hope that your serum isn't somehow compromised.

The serum we're talking about is FBS, Fetal Bovine Serum, which is derived from cow fetuses. It is blood that has been passed through a filter with tiny pores typically either 220 or 450 nanometers wide. These pores filter out cells and bacteria, creating a golden liquid with a complex mix of growth hormones and nutrients that help keep a mammalian cell culture alive.

Kajander and Ciftcioglu used 100-nanometer pores to produce a more pure serum, but still they found that their cell cultures were dying. They gamma-radiated the serum enough to kill any remnant bacteria, but again the serum was deadly to their cultures. Something had to be making it through the filter, but when they looked at the serum and tried to cultivate bacterial colonies, they invariably came up empty. Whatever was in the serum, it wasn't an ordinary bug. They were stumped, and went on to other research.

However, someone accidentally forgot a serum sample in the incubator, where it was left to slow cook for four months. When it was finally noticed, there was a slimy scum over the serum. Intrigued, they put the scum through some tests. They couldn't see anything interesting through the optical scope. But when they looked at it with a high-powered electron microscope, they were perplexed. It seemed that tiny bacteria had created a biofilm, a thin mat buttressed with deposits of the mineral apatite (calcium phosphate). But they were far too tiny, at least a hundredth of the size of normal bacteria. Whatever they were looking at had never been described in any of the microbiology literature.

When scientists see something that defies the current wisdom, they need to be extremely circumspect. This is especially true in biology, where there are so many variables to control for that it's hard to rule out contamination. They ran dozens of experiments, dosing the tiny bacteria with antibiotics, disinfectants and radiation. They discovered that for such a tiny thing, it was pretty tough. One wag dubbed it Conan the Bacteria. Whatever it was, it was slow-growing. While bacteria might double their population in minutes, it seemed to take days for these new bugs to double. That would explain why they hadn't been able to culture anything on such a short time scale.

But time and again, when they let the serum incubate for a sufficient period of time, it would turn cloudy, indicating a slow but steady growth. Except for the size and the slow growth rate, these creatures seemed a lot like bacteria. Apparently unaware of Dr. Folk's work, in a rare instance of parallel naming, they dubbed them nanobacteria.

The more they looked, the more they saw nanobacteria. Even human blood seemed to be infected with nanobacteria. But if nanobacteria were building calcium phosphate shells while cruising through the bloodstream, that couldn't possibly be good. Kajander and Ciftcioglu looked at arterial plaque and kidney stones and found nanobacteria in both places. Perhaps heart disease and kidney stones both had a nanobacterial origin. In 1997, they decided to publish.

You don't announce that you've discovered a new form of life without stirring up a little excitement in the biological community. Most biologists were incredulous, but at least one scientist decided to replicate the work. Dr. John Cisar, a researcher at the NIH, undertook a study to find these tiny spheres in serum and saliva. Very quickly, he did - but he came to a conclusion completely at odds with the Finnish team. To Dr. Cisar, the nodules were simply crystalline aggregates, something that can happen with ordinary chemistry. In 2000, Dr. Cisar published his report, claiming that bacterial contamination was responsible for the organic aspects of the phenomena and that self-propagating apatite was responsible for the apparent growth of the nodules.

Not everyone agreed. In fact, self- propagating apatite might be just as amazing as nanobacteria. In science, if you want to debunk something outrageous, it's best not to be outrageous yourself. Nevertheless, Dr. Cisar's results convinced many scientists that Kajander and Ciftcioglu had jumped the gun and that nanobacteria were simply an artifact.

Putting further strain on their credibility, Drs. Kajander and Ciftcioglu formed a company based on their research. It promised to test for and treat nanobacterial infections in people. Put yourself in their shoes: if you believed you could create a cure for a deadly disease, wouldn't you proceed to do so? As good as their intentions may be, however, some scientists suspect their objectivity might be colored by their business interests. The case for nanobacteria was tantalizing, they felt, but not sufficiently proven.

Don't Forget Texas


Thousands of nanobacteria crowd the inside wall of a diseased artery.
Credit: Credit: Lynch, Kirkland and Folk, University of Texas

Science is so big and diversified today that it's difficult to keep up with your own field, let alone an unrelated one. So when NASA announced the discovery of nanobacteria in the Martian meteorite, they had no idea that biologists in Finland were working on something similar. But an enterprising reporter for an Austin newspaper did a deep search for nanobacteria and came across the Finnish research. As Dr. Folk puts it, "This was great news both for me and for NASA -- independent confirmation by medical researchers of what ignorant geologists had thought they 'discovered.'" Soon after, NASA began cooperative work with some of the Finnish group.

In the meantime, Dr. Folk wasn't resting on his laurels. Supposedly retired, he continued to look under every rock for nanobacteria using the scanning electron microscope at the University of Texas. He was often successful. Along with Drs. Leo Lynch and Brenda Kirkland, he took hundreds of pictures (many of them have since been cataloged in a beautiful Photo Gallery by Dr. Lynch at Mississippi State University). One day, Dr. Kirkland brought in a sample of arterial plaque to put under the scope. They were surprised to see what looked like piles of nanobacteria coating the damaged artery. In 1997, they published the first photo of arterial plaque at 100,000 magnification.

By chance, they managed to hook up with the Mayo clinic. There were more than a few raised eyebrows at the prospect of these three geologists working on arterial plaque, but anyone who saw the pictures of plaque side-by-side with the pictures of travertine quickly got the connection. The biologists and the rock hounds complemented each other perfectly, and their research sped ahead.

Their hard work paid off in May of 2004 when the Mayo clinic announced that they had successfully repeated the Finnish experiments and added new data. Drs. John Lieske, Virginia Miller and their team ground up diseased human arteries and then filtered out everything smaller than 200 nanometers. That got rid of human cells and any ordinary bacteria. After a few weeks of incubation, they found increasing cloudiness in the serum. When it was examined with a high-power electron microscope, they saw small nodules, 20-200 nanometers in diameter, just as described by Kajander and Ciftcioglu. Interestingly, they found that the nodules absorbed uridine, one of the constituents of RNA.

They showed that particles filtered from genetically-caused aneurysms didn't show DNA activity, but particles from calcified aneurysms did. That implies that there is a living, replicating agent, under 200 nanometers in size, that is associated with a major cause of heart disease. Suddenly, nanobacteria were hot again.

The evidence is not indisputable. For instance, ordinary apatite crystals can soak up a little uridine all by themselves. And contaminants are always hard to rule out. But the Mayo team study helps to buttress the case for nanobacteria. Could it be that a slow-moving relic of the original primordial soup is still slinking around?

The First Earthlings?


A virus prepares to infect a normal bacteria; sausage-shaped nanobacteria are shown for scale.
© 2004 by Scott Anderson

A possible scenario starts to emerge: Billions of years ago, fed by the hot mineral springs that bubbled all over the early earth, different forms of pseudo-life started to emerge. Consisting of self-replicating RNA and simple proteins, these precursors to life were subject to the whims of their particular pond. With no cells walls, each genetic strand would depend on naturally-occurring amino acids to create proteins that might be shared by other bits of RNA or DNA. In a sense, the whole pond was the living creature. With much of the energy coming from thermal and chemical sources, there really weren't too many requirements for exotic metabolic proteins. It might be possible to create a replicating soup with just a few dozen genes.

Proteins are typically made of a small number of basic building blocks, like sheets and twisted ribbons. Great power comes from combining these small units into bigger complexes. Large-scale structures, like membranes and ribosomes, can be built simply by the continued addition of these basic bits. These larger objects typically require proteins to guide their construction. There might, however, be another way.

In a hot spring, currents set up when heat from below causes a plume of water to rise. When it hits the surface, it cools and then falls down the sides of the pool where it gets heated again.

Anything carried along with these currents would experience a regular cycle of heating and cooling. As it turns out, that's how scientists create working amounts of DNA in the lab: they heat a tiny sample, causing the paired strands of DNA to split apart. Then they let it cool, and as it does, chemicals in the mix reassemble a mirror image on each strand. The heating/cooling cycle is repeated, and for each temperature cycle the amount of DNA is doubled. After ten doublings, you have about 1,000 times more DNA than when you started. A hot spring might make an ideal incubator, delivering hot food to all parts of the pool and cycling through temperatures changes to encourage protein growth and genetic replication.

At some point, sheets large enough to serve as membranes may have formed. This would allow the formation of cells that could regulate their own affairs and separate their inner, cellular, chemistry from the rest of the pool. Separation had a big upside: if a pool changed in some fundamental way, the  blob of chemicals inside a membrane might outlive the unprotected life forms. But the membrane also brings problems: in order to really offer protection, it needs a bouncer at the door. The bouncer protein will let in the chosen molecules and turn away the rest. To create bouncers, though, you need extra genes, bringing the total up to sixty or so. These cells might look like mycoplasmas, tiny bacteria only 200 nanometers wide with a flimsy membrane. Still, with so much nutrition being cycled by the hot spring, the genetic needs of this creature would be small.

If one of these little creatures were somehow able to incorporate the abundance of dissolved calcium and phosphate into a tough shell, they might have an extra evolutionary advantage. They might even be able to survive the worst fate of such a pool - drying out. Such a bug could qualify as an ancestor of modern-day nanobacteria.

Jump ahead a few billion years to modern animals. With their hearts continuously delivering warm nutrients, including calcium and phosphate, a nanobacteria might find itself quite at home. As Kajander and Ciftcioglu put it, "The modern-day primordial soup is blood."

With the animal host doing most of the work, the nanobacteria would need just a minimal gene kit, keeping it very small and reducing its impact. Its slow growth rate wouldn't cause problems for the host for at least thirty or forty years - longer than the typical life span, and thus sparing it from Darwinian pressure.

Although this scenario is plausible, it is not the only one. Some scientists think nanobacteria have only recently taken up residence in human blood. Dr. Kajander points out that atherosclerotic plaque is a relatively new and growing cause of heart disease. As recently as 100 years ago, it was quite rare. On the other hand, people didn't live as long or eat as many French-fries back then either, so they may have had less of an opportunity to clog their arteries.

But whether nanobacteria are recent visitors or long-term residents, they seem to be up to no good. Their nastiness is twofold: they make hard shells and they cause human cells to die. The first wouldn't be so bad if it was limited to the bones, but hardness is not a desirable trait for a blood vessel. As to killing human cells, it may be excreted proteins that do the deed, but it is definitely bad manners for a guest. The possible ailments caused by nanobacteria include heart disease, kidney stones and cataracts. If Kajander and Ciftcioglu are correct, these maladies may yield to novel anti-nanobacterial medicines.

With so much at stake, the story of nanobacteria is not going to fade away. For the next few years we can expect to see many more studies like the one at Mayo. Hopefully, one of them will be able to sequence the DNA (or RNA). Only then will most scientists concede the existence of nanobacteria. Until then, it's bound to be an interesting journey.

Dr. Robert Folk responds:

Buongiorno, Scotto! Just finished your article -- congrats, a great job... But I wish you would credit Lynch and Kirkland as they are an integral part of the "Texas wing" of the connection between nannobacteria and heart disease -- geologists made a contribution as did medical researchers...

-- Ciao, RLFolk

A sign of a great scientist is eagerness to credit others. I've added more info about Drs. Lynch and Kirkland, both now at Mississippi State University.

-- Scott

Dr. Virginia Miller responds:

Dear Scott, Just finished reading your article and will add my congratulations to those of Dr. Folk. I think I reflect the collective enthusiasm of our group at Mayo by saying that working collaboratively on this project with the "Texas team" has been one of the most interesting and exciting projects of our careers. The results of this joint project are accepted for publication in the prestigious American Journal of Physiology: Heart and Circulatory Physiology, a peer reviewed journal published by the American Physiological Society.

-- Sincerely yours, Virginia Virginia M. Miller, PhD Professor, Surgery and Physiology

Here's a link to the article by Drs. Miller and Lieske (the abstract is free, the article requires a subscription or payment):

Mayo Clinic Study in the American Journal of Physiology

 http://ajpheart.physiology.org/cgi/search?sendit=Search&pubdate_year=&volume=&firstpage=&DOI=&author1=Lieske&author2=&title=&andorexacttitle=or&titleabstract=&andorexacttitleabs=and&fulltext=&andorexactfulltext=and&journalcode=ajpheart&fmonth=Jan&fyear=2003&tmonth=Jun&tyear=2004&fdatedef=1+January+1977&tdatedef=17+June+2004&flag=&RESULTFORMAT=1&hits=10&hitsbrief=25&sortspec=relevance&sortspecbrief=relevance

More links:

Mississippi State Nanobacteria Photo Gallery

Nanobac Life Sciences http://www.nanobaclabs.com/

The Calcium Bomb: The Nanobacteria Link to Heart Disease and Cancer

http://www.scienceforpeople.com/Essays/killer_nano.htm
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rawiron1
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« Reply #1 on: August 28, 2009, 07:29:45 AM »

In G.I. Joe Cobra Commander injects his sister's brain with nano-tech bugs to turn her into a mind controlled assassin.

Jason
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Harconen
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« Reply #2 on: August 28, 2009, 03:56:15 PM »

In G.I. Joe Cobra Commander injects his sister's brain with nano-tech bugs to turn her into a mind controlled assassin.

Jason

Thanks for info, I didn't see the movie. Strange...mind control & nano-tech. The topics on this site are so connected, like small parts of one big mosaic.
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« Reply #3 on: August 28, 2009, 03:58:00 PM »

The topics on this site are so connected, like small parts of one big mosaic.

Ding! Ding!  Ding!

Everything starts coming together after a while, doesn't it?

 Wink
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« Reply #4 on: August 28, 2009, 04:10:50 PM »

It seems like such benevolent altruistic research on medical uses for nanotechnology.. the problem is, big bucks for this kind of research always seem to come from defense spending... so today it's a mouse...

Nanotech Particles Affect Brain Development In Mice
http://www.sciencedaily.com/releases/2009/07/090728201737.htm

ScienceDaily (July 30, 2009) — Maternal exposure to nanoparticles of titanium dioxide (TiO2) affects the expression of genes related to the central nervous system in developing mice. Researchers found that mice whose mothers were injected with the nanoparticles while pregnant showed alteration in gene expression related to neurological dysfunction.

Ken Takeda led a team of researchers from the Tokyo University of Science, Japan, who carried out the tests. He said, "Nanotechnology and the production of novel man-made nanoparticles are increasing worldwide. Titanium dioxide in its nanoparticle form has a high level of photocatalytic activity, and can be used for air and water purification and self-cleaning surfaces. Our findings, however, add to the current concern that this specific nanomaterial may have the potential to affect human health".

For this study, the researchers injected pregnant mice with Ti02 nanoparticles. The brains were obtained from male fetuses/pups on the 16th day of gestation and at several points after birth. Comparing these brains to those of control animals, the researchers were able to demonstrate changes in expression of hundreds of genes. According to Takeda, "Diseases associated with these genes include those we normally consider to develop in childhood, such as autistic disorder, epilepsy and learning disorders, and also others that arise mainly in adulthood or old age, such as Alzheimer's disease, schizophrenia and Parkinson's disease."

Nanotechnology deals with engineering at the molecular scale. Materials reduced to nanoparticles behave in ways dissimilar to those we're used to - altering their reactivity, surface area to volume and any number of other properties. While larger TiO2 particles are commonly used in paints and sunblocks, nanoparticles of TiO2 are specially created for new applications in coatings and self-cleaning surfaces and their effects on living tissue are only beginning to be understood. It should be noted that this gene expression data cannot be interpreted as a direct health effect. In addition, the nanoparticles were deliberately injected at a high dose, so the relevance to real-life exposure may be limited.
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« Reply #5 on: August 28, 2009, 04:13:26 PM »

I wonder how many types of nanobacterial they'll be putting in the flu vaccines?
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« Reply #6 on: August 28, 2009, 04:26:48 PM »

I wonder how many types of nanobacterial they'll be putting in the flu vaccines?

My thoughts too... they used the word "inject" ...
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« Reply #7 on: August 28, 2009, 04:28:21 PM »

Morgellons: Mind Control Disease?



Sorcha Faal http://www.whatdoesitmean.com/index689.htm has an interesting post on Morgellons, which she calls a "Quantum" disease.

I was looking at these pictures of a Morgellons specimen and thought that they look somewhat similar to the things that were pulled out of a man named David A. Larson at us-government-torture.com. http://www.us-government-torture.com/ That website has something called The Larson Report. which details how this guy had found all these strange electrodes inside his body, many of them microsopic.

Here is a Morgellons Specimen:



People who had these implants that Larson had also had hallucinations of many kinds, heard voices, etc. Quite possibly, the two could be related.





These things are really weird. Sorcha Faal thinks that they are a Quantum Disease - a physical manifastation of something more metaphysical:

"The knowing of these Western governments too is that there is no earthly cure for these parasites that turn human beings into ‘wool’ to be eaten by the ‘worms’. For the curing of these worms, and as we well know, is to the spirit, the soul, and by the proper saying of the ancient words, of which they (governments) know but will not tell them to their peoples for their fear in letting this knowledge be known.

Even to the ancient philosopher Plotinus were known these things, and as said about him by Dr. Michael Hornum from the United States Bryn Mawr University, "Our higher self does not lie within us, as if an internal organ, or hover somewhere about the galaxy, but is present to each of us with an intimacy closer than any corporeal thing can have."



But these strange fibers are very weird - what if these things are a nano-technology experiment? Have a look at what was pulled out of Larson's body:


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« Reply #8 on: August 28, 2009, 04:30:09 PM »

Morgellons: Mind Control Disease?



Sorcha Faal http://www.whatdoesitmean.com/index689.htm has an interesting post on Morgellons, which she calls a "Quantum" disease.

I was looking at these pictures of a Morgellons specimen and thought that they look somewhat similar to the things that were pulled out of a man named David A. Larson at us-government-torture.com. http://www.us-government-torture.com/ That website has something called The Larson Report. which details how this guy had found all these strange electrodes inside his body, many of them microsopic.

Here is a Morgellons Specimen:



People who had these implants that Larson had also had hallucinations of many kinds, heard voices, etc. Quite possibly, the two could be related.





These things are really weird. Sorcha Faal thinks that they are a Quantum Disease - a physical manifastation of something more metaphysical:

"The knowing of these Western governments too is that there is no earthly cure for these parasites that turn human beings into ‘wool’ to be eaten by the ‘worms’. For the curing of these worms, and as we well know, is to the spirit, the soul, and by the proper saying of the ancient words, of which they (governments) know but will not tell them to their peoples for their fear in letting this knowledge be known.

Even to the ancient philosopher Plotinus were known these things, and as said about him by Dr. Michael Hornum from the United States Bryn Mawr University, "Our higher self does not lie within us, as if an internal organ, or hover somewhere about the galaxy, but is present to each of us with an intimacy closer than any corporeal thing can have."



But these strange fibers are very weird - what if these things are a nano-technology experiment? Have a look at what was pulled out of Larson's body:




Oh no Harconen... that's a Sorcha Faal disinfo site. Sad
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« Reply #9 on: August 28, 2009, 04:31:57 PM »

Ding! Ding!  Ding!

Everything starts coming together after a while, doesn't it?

 Wink

Yes it does. Like in twilight zone, but it is real.
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« Reply #10 on: August 28, 2009, 04:34:56 PM »

Oh no Harconen... that's a Sorcha Faal disinfo site. Sad

Is it? OK. but other things from http://www.us-government-torture.com/ are not disinfo.
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Resist. Rebel. Cry out to all peoples and nations from the sky as the lightening flashes from the east to the west and judge the living and the dead.Or choose submission and slavery.

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« Reply #11 on: August 28, 2009, 04:52:14 PM »

I wonder how many types of nanobacterial they'll be putting in the flu vaccines?

Now they can put whatever they wont. See this.

Like burrs on your clothes, virus-size capsules stick to cells to target drug delivery
June 25, 2009
http://www.news.cornell.edu/stories/June09/GeneTherapy.html

It is now possible to engineer tiny containers the size of a virus to deliver drugs and other materials with almost 100 percent efficiency to targeted cells in the bloodstream.

According to a new Cornell study, the technique could one day be used to deliver vaccines, drugs or genetic material to treat cancer and blood and immunological disorders. The research is published online at the Web site of the journal Gene Therapy.


Zhong Huang/Cornell University
This image shows a microtube surface coated with nanocapsules containing a small-interfering RNA (which glows red under a fluorescent microscope). The capsules were targeted to specific circulating cells.

"This study greatly extends the range of therapies," said Michael King, Cornell associate professor of biomedical engineering, who co-authored the study with lead author Zhong Huang, a former Cornell research associate who is now an assistant professor at the Shenzhen University School of Medicine in China. "We can introduce just about any drug or genetic material that can be encapsulated, and it is delivered to any circulating cells that are specifically targeted," King added.


nanocapsules ingested by cells
Zhong Huang/Cornell University
This image shows that after 36 hours nearly every target cell (round gray spheres) has ingested a nanocapsule containing a small-interfering RNA (in red).

The technique involves filling the tiny lipid containers, or nanoscale capsules, with a molecular cargo and coating the capsules with adhesive proteins called selectins that specifically bind to target cells. A shunt coated with the capsules is then inserted between a vein and an artery. Much as burrs attach to clothing, the selectin-coated capsules adhere to targeted cells in the bloodstream. After rolling along the shunt wall, the cells break free from the wall with the capsules still attached and ingest their contents.

The technique mimics a natural immune response that occurs during inflammation, which stimulates cells on blood vessel walls to express selectins, which quickly form adhesive bonds with passing white blood cells. The white blood cells then stick to the selectins and roll along the vessel wall before leaving the bloodstream to fight disease or infection. Selectin proteins may be used to specifically target nucleated (cells with a nucleus) cells in the bloodstream.

The study shows that since only the targeted cells ingest the contents of the nanocapsules, the technique could greatly reduce the adverse side effects caused by some drugs.

In a previous paper, King showed how metastasizing cancer cells circulating in the blood stream can stick to selectin-coated devices containing a second protein that programs cancer cells to self-destruct.

Said King, "We've found a way to disable the function of cancer cells without compromising the immune system," which is a problem with many other therapies directed against metastasis.

The current study demonstrates that genetic material can be delivered to targeted cells to turn off specific genes and interfere with processes that lead to disease. The researchers filled nanocapsules with a small-interfering RNA (siRNA) and targeted them to specific circulating cells. When the targeted cells ingested the capsules, the siRNA turned off a gene that produces an enzyme that contributes to the degradation of cartilage in arthritis.

In a similar manner, the method could be used to target the delivery of chemotherapy drugs, vaccine antigens to white blood cells, specific molecules that mitigate auto-immune disorders and more, King said.

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« Reply #12 on: August 29, 2009, 10:16:11 AM »

Awesome post. Thank you. Smiles.
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« Reply #13 on: August 29, 2009, 03:20:16 PM »

Nano-Mind Control


http://www.youtube.com/watch?v=uf6EGvl7nJo
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« Reply #14 on: August 29, 2009, 05:09:33 PM »

Quote
NanoCapsules containing a small-interfering RNA
"This study greatly extends the range of therapies," said Michael King, Cornell associate professor of biomedical engineering, who co-authored the study with lead author Zhong Huang, a former Cornell research associate who is now an assistant professor at the Shenzhen University School of Medicine in China. "We can introduce just about any drug or genetic material that can be encapsulated, and it is delivered to any circulating cells that are specifically targeted," King added

I feel like the guy in Aliens "Its all over and I had only two weeks left"
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« Reply #15 on: August 29, 2009, 05:43:22 PM »

Nanobot.info Report on Nanobots (Nanotechnology Robots)

http://www.nanobot.info/




Basic nanomachines are already in use. Nanobots will be the next generation of nanomachines. Advanced nanobots will be able to sense and adapt to environmental stimuli such as heat, light, sounds, surface textures, and chemicals; perform complex calculations; move, communicate, and work together; conduct molecular assembly; and, to some extent, repair or even replicate themselves. Nanobot.info is an informational site that provides information on both recent developments and future applications at the intersection of nanotechnology and robotics. Nanotechnology is the science and application of creating objects on a level smaller than 100 nanometers.  The extreme concept of nanotechnology is the "bottom up" creation of virtually any material or object by assembling one atom at a time.  Although nanotech processes occur at the scale of nanometers, the materials and objects that result from these processes can be much larger.   Large-scale results happen when nanotechnology involves massive parallelism in which many simultaneous and synergistic nanoscale processes combine to produce a large-scale result.

Nanotechnology spans and merges disciplines dealing with matter at the micro level (physics, chemistry, and biology) with those dealing with matter at the macro level (engineering, materials science and computer science).

Nanotechnology coatings are already being used to make clothing with stain-resistant fibers.  Nanotech powders are already being used to formulate high-performance sun-screen lotions.  Nanoparticles are already helping to deliver drugs to targeted tissues within the body.  Additional applications are underway in the areas of: medical diagnosis and treatments; biotechnology; advanced development of pharmaceuticals; cosmetics; aerospace and automotive industries; security, defense, and environmental protection; electronics, computers and communication; energy production, storage, and lighting; and manufacturing and product design.  Also see -- Open Directory - Science: Technology: Nanotechnology. http://www.dmoz.org/Science/Technology/Nanotechnology/

Nanomanufacturing is the creation of materials and products through: (1) Direct Molecular Assembly (DMA) -- discrete, directed assembly of individual atoms and molecules into macroscale materials and products; (2) Indirect Crystalline Assembly (ICA) -- creation of conditions that foster the growth of nanoscale crystals that are then combined into macroscale materials and products; or (3) Massive Parallelism Assembly (MPA) -- the creation of many nanomachines or nanobots whose operating parameters cause them to work synergistically to assemble atoms and molecules into macroscale materials and products.

What defines life?  Is it the ability to …reproduce? … adapt to the environment?  …think and learn?  Or is life determined by structure and origin rather than function and ability?  Nanotechnology may be able to create nanobots that emulate certain  functions of biological entities, but the structures and origin of nanobots will likely remain quite different than those of biological entities.  See also Virtual Basketball Game. http://www.virtualbasketballgame.com/

Nanotechnology has the potential to completely revolutionize the electronics industry.  Nanomachines may some day create computer circuits from the “bottom up” -- one atom at a time. This would allow the manufacturing of nanochips on a much smaller scale than chips created with current “top down” etching techniques.  Nanocrystalline processes can also be used to grow electronics components.  For example: (1) carbon nanotubes grown in targeted micro-environments can have super-conductive properties; and (2) nanowires as small as strings of atoms can be grown like crystals and then assembled into circuits.  Circuits created atom-by-atom or grown using nanocrystalline techniques will be much smaller, lighter, efficient, cooler, stronger, and faster than circuits made with conventional manufacturing processes.

Nanotechnology has numerous energy-related applications.  Nanophotonics is the application of nanotechnology to the transformation of electricity to light or light to electricity.  In this area, nanocrystals or nanophosphores can make this transformation with greater efficiency than traditional incandescent lighting or solar panels.  Using nanoceramic material as the covering for batteries absorbs electromagnetic waves and prolongs battery life.  Nanopolymers provide high-performance insulation for energy transmission lines and decrease energy loss across long distances.  Also interesting, Pacific Northwest National Laboratory. http://www.pnl.gov/nano/

In the telecommunications industry, nanotechnology will play an important role in the coming years particularly with respect to fiber optics.  Nanocrystalline materials can be made with finer resolution than standard fibers for enhanced optic cables, switches, lenses and junctions.  In telecommunications more generally, the fields of nanotechnology and holotechnology will overlap in the design of the projection screens and user interfaces of the next generations of holographic cell phones, “Holographones,” and televisions, “HoloTVs.”  More Virtual Reality. http://www.virtualrealities.info/

Many human illnesses and injuries have their origins in nanoscale processes.  Accordingly, application of nanotechnology to the practice of medicine and biomedical research opens up new opportunities to treat illnesses, repair injuries, and enhance human functioning beyond what is possible with macroscale techniques.  At the nanoscale level, the distinctions between mechanical and biological processes blur.  Nanoparticles can attach to certain cells or tissues and provide medical images of their location and structure.  Hollow nanocapsules with pharmaceutical contents can attach to cancer cells and release their payloads into them – maximizing targeted delivery and minimizing systemic side effects.  Nanomedibots may repair vital tissue damanged by injury or disease, or destroy cancerous tissue that has gone awry, without invasive surgery.  More Nanostream. http://www.nanostream.com/

Nanopharmacology is the application of nanotechnology to the discovery of new molecular entities with pharmacological properties.  Nanotechnology is also useful for individualized matching of pharmaceuticals to particular people to maximize effectiveness and minimize side effects.  It is also used for  delivery of pharmaceuticals to targeted locations or specific types of tissue in the body.
Nanotechnology is already being used for several sports and recreation related applications.  For example, nanotech tennis rackets and golf clubs are lighter, stronger, and can be engineered to provide more motion control.  Nanotech coatings on swim suits repel water, reduce friction with the water, and allow swimmers to go faster.

There are promising applications of nanotechnology in the field of orthopedics.  Grafts of natural bone can carry disease or trigger immune rejection by the host.  If one sterilizes the bone to reduce the chances of disease, then this can weaken the bone.  Artificial bone cement without nanotechnology can work for small applications, but tends to not have sufficient strength for load-bearing bone replacement.   However, artificial bone paste made with nanoceramic particles shows considerable promise for bone repair and replacement, even in load-bearing applications.  Additional http://nanojournal.nano-tek.org/.

In addition to delivering pharmaceuticals as discussed above, nanotech medical robots ("nanomedibots") may be able to: monitor body function; repair damaged tissue at the molecular level; deconstruct pathologic or abnormal material or cells such as cancer or plaque; and enhance human health and functioning. Although nanomedibots have not been developed, there are ongoing advances in nanofluidics and carbon nanotube flow sensors that may become their building blocks.  As nanotechnology and biotechnology advance, nanomedibots and engineered beneficial microorganisms may be integrated.
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« Reply #16 on: August 29, 2009, 05:49:40 PM »

Nanotech Companies

http://www.nanotechcompanies.us/

Nanotech, short for nanotechnology, refers to technological developments on the nanometer scale, usually in the range of 0.1 to 100 nanometers.  One nanometer is equal to one-thousandth of a micrometer or one-millionth of a millimeter.  At this microscopic size, physical phenomena such as quantum mechanics size effects and Van der Waals force effects are observed, which are not observed on the macroscopic scale.

In 1974, Professor Norio Taniguchi, of Tokyo Science University, first defined the term "nanotechnology" as the "processing, separation, consolidation, and deformation of materials by one atom or one molecule".  In a broader sense, nanotechnology is used to create structures on a scale below 100 nanometers, making possible the rapid development of technological advances on the molecular scale.

medical nanotech bots This field is becoming increasingly important with the rapidly changing electronics and mechanical industries.  As products become smaller, the challenges in design and manufacturing rise rapidly.  With this technology, currently cumbersome mechanical devices in fields as diverse as biotechnology, medicine, electronics, and others will be replaced with sophisticated microscopic devices capable of doing things that are only imagined today.  As nanotechnology develops, new products are brought to market that are more user friendly, portable, and flexible in their applications.  In a general sense, nanotechnology has the same effect on mechanical devices that advanced miniaturization in electronics has had on super computers, enabling them to shrink to the size of a laptop or PDA.  It is expected that the nanotech field will continue to show dramatic growth in the foreseeable future.

The directory of nanotechnology companies listed on Nanotech Now and the representative nanotech companies listed below exemplify business and research trends in this exciting field.
Nanotech Companies

    * IBM Research
      IBM's nanotech research aims to devise new atomic-scale and molecular-scale structures and devices for enhancing information technologies, as well as discover and understand their scientific foundations.
      Domino.Research.IBM.com

    * Ardesta
      A leader in bringing Small Tech and Nano Tech products to the global marketplace.
      www.Ardesta.com

    * Nano Opto
      This nanotech company creates new classes of densely integrated, modular nano-optic components.
      www.NanoOpto.com

    * Nanomix
      "Reducing Nanotechnology to Practice". Working to develop and commercialize new products made from nanoscale materials and components.
      www.Nano.com

    * Nanocrystal Technology
      Manufactures drug delivery solutions offering enhance absorption rates and bioavailability.
      www.Elan.com

    * Pacific Nanotechnology
      Provides products and services that facilitate advances in nanotechnology and nanoresearch.
      www.PacificNanotech.com

    * Versilant
      Pioneering the invention, development, and production of nanotechnology-based materials.
      www.Versilant.com

    * Zyvex
      Molecular nanotechnology company with applications in the areas of Materials, Tools, and Structures.
      www.Zyvex.com

    * NanoDynamics
      This leading nanotech company manufactures nanomaterials that may dramatically improve the form, function and performance of a wide range of consumer and industrial products.
      www.NanoDynamics.com

Nanotechnology Resources

    * National Nanotechnology Initiative
      Multi-agency framework to ensure U.S. leadership in nanotechnology.
      www.Nano.gov

    * Nanotech Project
      The Project on Emerging Nanotechnologies is dedicated to helping ensure that risks are minimized, public and consumer engagement remains strong, and potential benefits are realized as nanotechnologies continue to advance.
      www.NanotechProject.org

Related Nanotech Resource

    * Nanotechnology Investments - government and academic nanotechnology investing.
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« Reply #17 on: August 29, 2009, 06:36:37 PM »

A loaded gun


The Telegraph provides a quick survey of some leading scientists' thoughts about the future, as we move "from being passive observers of nature to its choreographers." As with most predictions about the course of technological change, the forecasts split fairly neatly between the utopian and the dystopian. The divide is captured well in the vision of nanotechnology presented by a professor at the US Joint Special Operations University:

    On the battlefield, nanobots are going to do a lot of things; they can seek and destroy specific targets, for instance. You've heard about the 'surgeon" that you can inject into your bloodstream – well, they can go in there to repair a clogged blood vessel, or they might be able to go in and punch holes in the blood vessels to destroy an adversary. The embryonic stages are here today, and a lot of work is being done.

An Oxford professor elaborates:

    With an advanced form of nanotechnology, it would be possible to build different kinds of weapons systems for which it's very difficult to see how an effective defence would be possible. In my view, the advanced form of nanotechnology is arguably the greatest existential risk humanity is likely to confront in this century.

The prospect of gaining greater control over our biological and genetic destiny produces similarly divided predictions. Ray Kurzweil foresees an end to disease, as we "reprogram biology away from cancer, away from heart disease, to really overcome the major diseases that kill us." But Francis Collins wonders whether only an elite will be able to afford to turn themselves into the new supermen:

    Suppose we develop – by our understanding of how the genome works and therefore how the body works – an approach that would improve memory; what's wrong with that? Well, it raises the question of who decides what's an improvement, and is that something that is going to be available to all or will it be another example of separating between people who have resources and people who don't?

Adds Eliezer Yudkowsky, of the Singularity Institute: "We have a choice in how we create artificial intelligence. And you've got to be very sure that a created mind is never going to want to self-improve and that it's never going to want to do anything that destroys intelligent life. You've got to treat that gun as if it's loaded."

Our ability to fiddle with nature comes at a time when we are increasingly removed from nature. That seems to be particularly true of children. "It seems obvious," writes Leonie Maistre, "that children need nature but it is fast becoming evident that children, who are the treasure of any society and its future, are being starved of it and all that nature has to offer." Peter Fimrite, of the San Francisco Chronicle reports on how nature is, for many kids, being disintermediated by digital media:

    The notion of going on a hike, camping, fishing or backpacking is foreign to a growing number of young people in cities and suburbs around the nation, according to several polls and studies. State and national parks, it seems, are good places for old folks to go, but the consensus among the younger set is that hiking boots aren't cool. Besides, images of nature can be downloaded these days.

    It isn't just national forests and wilderness areas that young people are avoiding, according to the experts. Kids these days aren't digging holes, building tree houses, catching frogs or lizards, frolicking by the creek or even throwing dirt clods. "Nature is increasingly an abstraction you watch on a nature channel," said Richard Louv, the author of the book "Last Child in the Woods," an account of how children are slowly disconnecting from the natural world. "That abstract relationship with nature is replacing the kinship with nature that America grew up with."

It seems unlikely that people who's conception of "nature" is almost entirely abstract will have many qualms about pulling the loaded gun's trigger. It's just another mashup.

http://www.roughtype.com/archives/2007/10/a_loaded_gun.php
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« Reply #18 on: August 29, 2009, 06:48:44 PM »

Tiny Brain-Like Transistor Controls Nanobots



The wheel-like assembly of 16 duroquinone molecules on the edges and 1 duroquinone molecule in the center can produce "one-to-many" parallel communication. Credit: Bandyopadhyay and Acharya.

For years, researchers have been building tiny nanobots that could one day serve a variety of purposes. But, until now, nanobots couldn't work together.

Recently, scientists Anirban Bandyopadhyay and Somobrata Acharya from the National Institute of Materials Science in Tsukuba, Japan, have built the first ultra-tiny, ultra-powerful "brains" for nanobots.

The brains - just two billionths of a meter across - act as tiny computer transistors. But instead of carrying out just one operation at a time, like a normal transistor, the new devices can simultaneously perform 16 operations at once. In other words, the devices use parallel processing - like the human brain - rather than serial processing - like a normal computer. The researchers call this ability "one-to-many" communication.

The tiny machines are composed of 17 duroquinone molecules that act as logic gates. The researchers arranged 16 of these molecules in a wheel, and placed the last molecule in the middle, which acts as the control center. The entire wheel was constructed on a gold substrate.

Each duroquinone molecule has four side chains that can be independently rotated to represent four separate logic states. Conventional transistors, on the other, have just two logic states: on and off.

To operate the device, the researchers poked the center duroquinone molecule with electrical pulses from the tip of a scanning tunneling microscope. The center molecule is linked to the surrounding 16 molecules by weak hydrogen bonds, so that a pulse to the center molecule can simultaneously transmit instructions to each of the surrounding molecules.

Since each molecule has four side chains, a single pulse to the center molecule can produce one of nearly 4.3 billion (4^16) different states. That compares with a total of 2 (2^1) states that can be produced in a conventional transistor. However, some instructions from the center molecule result in particular arrays of molecules that take on fixed states to maintain equilibrium. But, in principle, the system has 4.3 billion possible states.

Banyopadhyay and Acharya aren´t stopping there, though. The team plans to turn the 2D wheel of 16 molecules into a 3D sphere - a structure that would consist of 1,024 molecules. This spherical device could perform 1,024 instructions at once, theoretically making it capable of 4^1024 different states. The center molecule could be controlled with "handles" that stick out of the core.

The researchers also tested out the 2D nano-brain in their study. They attached the device to eight nanobots (sometimes called "molecular machines"), and demonstrated that the nanobots could respond simultaneously to a single instruction. The ´bots could work together, as if part of a tiny factory.

The scientists also created the "world´s tiniest elevator," a 2-nanometer-tall device that can move up and down by 1 nanometer. They also plan to hook up the brain to a variety of nano-sized motors, propellers, switches, and sensors for different applications.

In the future, the researchers hope that they can control the central duroquinone molecule using proteins or other molecules, rather than the scanning electron microscope tip. For one thing, this ability might enable the brains to serve as tiny transistors packed onto a microchip for future powerful computers.

More futuristically, the brains could accompany nanobots for medical missions, such as bloodless surgery. As the scientists explain, specialized molecular machines could travel through veins to a tumor or damaged tissue, and perform surgery according to the instructions given by the new brains.

More information: Bandyopadhyay, Anirban and Acharya, Somobrata. "A 16-bit parallel processing in a molecular assembly." Proceedings of the National Academy of Sciences. March 11, 2008, vol. 105, no. 10, 3668-3672.

http://www.physorg.com/news124537060.html
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« Reply #19 on: August 29, 2009, 07:34:14 PM »

Tiny Brain-Like Transistor Controls Nanobots



The wheel-like assembly of 16 duroquinone molecules on the edges and 1 duroquinone molecule in the center can produce "one-to-many" parallel communication. Credit: Bandyopadhyay and Acharya.

For years, researchers have been building tiny nanobots that could one day serve a variety of purposes. But, until now, nanobots couldn't work together.

Recently, scientists Anirban Bandyopadhyay and Somobrata Acharya from the National Institute of Materials Science in Tsukuba, Japan, have built the first ultra-tiny, ultra-powerful "brains" for nanobots.

The brains - just two billionths of a meter across - act as tiny computer transistors. But instead of carrying out just one operation at a time, like a normal transistor, the new devices can simultaneously perform 16 operations at once. In other words, the devices use parallel processing - like the human brain - rather than serial processing - like a normal computer. The researchers call this ability "one-to-many" communication.

The tiny machines are composed of 17 duroquinone molecules that act as logic gates. The researchers arranged 16 of these molecules in a wheel, and placed the last molecule in the middle, which acts as the control center. The entire wheel was constructed on a gold substrate.

Each duroquinone molecule has four side chains that can be independently rotated to represent four separate logic states. Conventional transistors, on the other, have just two logic states: on and off.

To operate the device, the researchers poked the center duroquinone molecule with electrical pulses from the tip of a scanning tunneling microscope. The center molecule is linked to the surrounding 16 molecules by weak hydrogen bonds, so that a pulse to the center molecule can simultaneously transmit instructions to each of the surrounding molecules.

Since each molecule has four side chains, a single pulse to the center molecule can produce one of nearly 4.3 billion (4^16) different states. That compares with a total of 2 (2^1) states that can be produced in a conventional transistor. However, some instructions from the center molecule result in particular arrays of molecules that take on fixed states to maintain equilibrium. But, in principle, the system has 4.3 billion possible states.

Banyopadhyay and Acharya aren´t stopping there, though. The team plans to turn the 2D wheel of 16 molecules into a 3D sphere - a structure that would consist of 1,024 molecules. This spherical device could perform 1,024 instructions at once, theoretically making it capable of 4^1024 different states. The center molecule could be controlled with "handles" that stick out of the core.

The researchers also tested out the 2D nano-brain in their study. They attached the device to eight nanobots (sometimes called "molecular machines"), and demonstrated that the nanobots could respond simultaneously to a single instruction. The ´bots could work together, as if part of a tiny factory.

The scientists also created the "world´s tiniest elevator," a 2-nanometer-tall device that can move up and down by 1 nanometer. They also plan to hook up the brain to a variety of nano-sized motors, propellers, switches, and sensors for different applications.

In the future, the researchers hope that they can control the central duroquinone molecule using proteins or other molecules, rather than the scanning electron microscope tip. For one thing, this ability might enable the brains to serve as tiny transistors packed onto a microchip for future powerful computers.

More futuristically, the brains could accompany nanobots for medical missions, such as bloodless surgery. As the scientists explain, specialized molecular machines could travel through veins to a tumor or damaged tissue, and perform surgery according to the instructions given by the new brains.

More information: Bandyopadhyay, Anirban and Acharya, Somobrata. "A 16-bit parallel processing in a molecular assembly." Proceedings of the National Academy of Sciences. March 11, 2008, vol. 105, no. 10, 3668-3672.

http://www.physorg.com/news124537060.html

Damn, that is beyond Science Fiction.
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« Reply #20 on: August 29, 2009, 07:42:06 PM »

Nanobots Flowing Through a Blood Vessel
http://vodpod.com/watch/1356646-nanobots-flowing-through-a-blood-vessel?pod=vinithbejugam


Nanobots
http://vodpod.com/watch/1356645-nanobots?pod=vinithbejugam


Nanobots replacing neurons
http://vodpod.com/watch/1356644-nanobots-replacing-neurons?pod=vinithbejugam
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« Reply #21 on: August 29, 2009, 08:00:04 PM »

Nano, the next dimension (Film produced for European Commission)

http://www.youtube.com/watch?v=eCpkq_AeX50&feature=fvw



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« Reply #22 on: August 29, 2009, 08:30:10 PM »

Ewww....Sperm Could Power Nanobots

Scientists look to sperm to power nanobots


In the future, when your kids ask how all those millions of "nano-bots" swim through your blood....don't tell them the truth.


By Bryn Nelson
Columnist
msnbc.com contributor
updated 9:32 a.m. ET Jan. 2, 2008
http://www.msnbc.msn.com/id/22333518/

A tiny assembly line that powers the whip-like tail of sperm could be harnessed to send future nanobots or other tiny medical devices zooming around the human body, according to a preliminary research report.

Borrowing a page from reproductive biology, the proof-of-principle study offers a peek at how nanotechnology might overcome the problem of supplying energy to the envisioned menagerie of nanobots, implants and “smart” probes aimed at releasing disease-fighting drugs, monitoring enzymes and performing other medical roles within a patient’s body.

To be biologically compatible, these hypothetical devices would need to be formed not from tiny springs and nuts and bolts but from biomedical components. “At that scale, biology provides the best functional motors,” said Alexander Travis, an assistant professor of reproductive biology at Cornell University’s Baker Institute for Animal Health. “But how do you power these kinds of structures?”

One potential answer has come from the tail, or flagellum, that propels human sperm at a rate of about 7 inches per hour. (In comparison, if a 6-foot man swam the equivalent number of body lengths in an hour, his tally of 3.7 miles would smash the American long-distance swimming record.)

To supply the energy for its locomotion, a sperm cell’s tail is essentially studded with tiny assembly lines that produce a high-energy compound called ATP. Officially known as adenosine triphosphate, ATP has been called the universal energy “currency” of living cells because of its ability to store, transfer and release energy. When a power source is needed to run processes within a cell — say, bending and flexing a sperm’s flagellum — ATP releases its reserves through a process that results in its decay to a simpler chemical form.

The most efficient producers of ATP are mitochondria, the cell’s miniature power plants. Sperm tails contain a spiraling helix of these mitochondria within the area closest to the sperm’s head. On the remaining three-quarters of its tail, however, the cell uses an approach based on a pathway called glycolysis, in which sugar is broken down into several components, including high-energy ATP molecules.

Proteins normally require the freedom to twist, bend or change shape to be functional. Research by Travis and Cornell colleague Chinatsu Mukai, together with other scientists, suggests that in sperm, the 10 proteins involved in glycolysis have been tweaked so they stick to a solid scaffold-like support running the length of the tail while still maintaining their activity. Travis and Mukai borrowed that approach to re-jigger the proteins so they stuck instead to the surface of a tiny gold chip covered with nickel ions. For their research, the scientists used mouse sperm proteins as templates for the synthesized versions. (Human and mouse sperm proteins are closely related.)

After tethering the first two proteins in the pathway to the chip, the researchers found that both did well in breaking down glucose and handing the end-product to the next protein. Compared to versions lacking a surface-targeting domain and “just randomly glommed” onto a structural support, the engineered proteins performed especially well.  Most of the remaining assembly line has yet to be similarly tweaked, but Travis and Mukai’s work suggests it should be possible. “We believe it is one of the first, if not the first, example of building a biological pathway on a manmade surface,” Travis said. The collaborators have a provisional patent for the ATP-making strategy, though no commercial partners as of yet.

Like a vehicle running on gasoline, the sperm’s power production emits waste. Fortunately, its tail harbors a transport protein that acts like a tailpipe to kick out waste and keep the production cycle going. Future nanodevices, Travis said, could include this transporter to similarly maintain their energy production. Maximizing the pathway’s efficiency could prove important for future strategies, such as filling tiny delivery capsules known as liposomes with cancer-fighting drugs and studding their outsides with antibodies that would direct the medical packets to attack specific tumor cells. Under that scenario, a steady supply of ATP could power the pumps charged with dispensing the medication at a certain rate.

Other scientists are likewise mining the emerging field of nanotechnology and its largely unrealized potential for delivering high-impact devices in ultra-small dimensions. Recent studies, for example, have harnessed nanotubes, nanodiamonds and magnetic nanoparticles for drug delivery (but not yet within humans). One group has created a tiny nickel-based rod that spins almost like a tiny propeller as it uses ATP. Another team, led by Carlo Montemagno at the University of Cincinnati, is working on a technique that makes ATP from light photons.

As a veterinarian, Travis said his interest in wildlife conservation got him into reproductive biology and research aimed at fighting infertility and exploring birth control methods. Through efforts by his lab and others, he discovered that one of the most abundant proteins in mammalian sperm, hexokinase, is also the first enzyme in the glycolysis assembly line on its tail. That observation led to questions about the protein’s role, location and, eventually, about whether it and its assembly line partners might be useful for other applications. 

Cornell University’s emphasis on nanotechnology “just kind of clicked” with his reproductive biology research, Travis said. He and Mukai presented the initial results from that scientific pairing in early December at the American Society for Cell Biology’s annual meeting, held in Washington, D.C., and are now preparing the study for publication.

Dr. Erkki Ruoslahti, a nanotechnology researcher and distinguished professor with the La Jolla, Calif.-based Burnham Institute for Medical Research, said he was intrigued by the approach and considered it a valid first step. “It sounds good to me — that’s the kind of thing that the field needs,” he said. “Having some sort of way of being able to power nanodevices is the number one bottleneck in constructing really clever devices.”

The safety of nanotechnology devices has yet to be fully resolved. Ruoslahti cautioned that sperm-inspired ATP generators would need to overcome the likelihood that the altered proteins would be recognized as foreign by the body’s immune system, provoking a strong immune response. Even so, he pointed out that some nanoparticles potentially serving as the basis for savvy devices of the future are already in use, including magnetic iron oxide particles used for advanced body imaging. “These are not pie-in-the-sky technologies,” Ruoslahti said. “They’re already with us.”
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« Reply #23 on: August 29, 2009, 08:49:49 PM »

Scientists Ready New Nanobots to Swim in Human Blood Stream

New mini robots soon to be injected into humans


Jason Mick, DailyTech
January 21, 2009
http://www.allhealthcare.com/news/articles/2909-scientists-ready-new-nanobots-to-swim-in-human-blood-stream

Modern medicine has yielded wonderful advances in cardiovascular surgery, which have saved many lives. Where blood clots or plaque on arteries too delicate for cut and sew operations were once untreatable and ultimately fatal, surgeons can now use catheters to reach many of these locations.

Unfortunately, though catheters have their shortcomings. When navigating narrow arteries, they can sometimes accidentally prick the wall, puncturing it and triggering a fatal bleed. And some areas, like cranial arteries in the brain, are to small and maze-like to reach with a catheter.

Enter the nanobots — scientists at Micro/Nanophysics Research Laboratory at Australia’s Monash University have developed tiny nanobot micromotors that are a mere quarter of a millimeter, powered by tiny piezoelectric motors, capable of swimming in the human bloodstream. They are putting the finishing touches on the motors and readying them for clinical tests on animals and, before long, humans.

While the team is still devising ways to remote control the new robots, they feel that they have a solid solution for an autonomous motor design in the form of piezoelectricity. Piezoelectricity is the ability of devices to generate electric pulses based on mechanical movement or vibrations. Piezoelectric devices include computer’s clocks, electric guitar pickups, electric stove lighters, and some inkjet printer heads.

In the human body, the flow of blood provides abundant kinetic energy. While a nanobot is too small to likely have a useful battery, it could exploit this kinetic energy to power tiny micromotors, the goal of the Australian researchers.

Professor James Friend, leader of the research team at Monash University explains, “Opportunities for micro-motors abound in fields as diverse as biomedicine, electronics, aeronautics and the automotive industry. Responses to this need have been just as diverse, with designs developed using electromagnetic, electrostatic, thermal and osmotic driving forces. Piezoelectric designs however have favourable scaling characteristics and, in general, are simple designs, which have provided an excellent platform for the development of micro-motors.”

He says motors have lagged behind other mechanical devices in development, stating, “If you pick up an electronics catalogue, you’ll find all sorts of sensors, LEDs, memory chips, etc that represent the latest in technology and miniaturisation. Take a look however at the motors and there are few changes from the motors available in the 1950s.”

The new micromotors will allow nanobots to reach places that previous minimally invasive surgery could not, like the human brain.

The team has developed prototypes of the micromotors, which they describe in a journal article found in the Journal of Micromechanics and Microengineering.

The next step is to develop more efficient assembly methods, and to devise ways to control the motors more accurately. The team’s work should be a natural fit, though for other researchers’ designs, which feature useful arterial nanobots, but lack a system of propulsion. The new work is similar to work by American researchers at Georgia Tech who are working to create blood-powered generators for implants.

© DailyTech 2009
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« Reply #24 on: August 29, 2009, 09:04:27 PM »

Nanobot Lets DNA Legs Do the Walking


08 January 2009 University of Oxford


A TWO-legged molecular machine that can walk unaided along a single strand of DNA could one day shift cargo around nanofactories. That's the promise of a walking molecular nanobot made by researchers at the University of Oxford.

Molecular engines that walk along strands of DNA are nothing new, but none has featured as many successful features as the Oxford team's device. Unlike earlier attempts, their nanobot doesn't wander aimlessly back and forth, fall off its track or destroy its track as it walks. The team have also devised an ingenious way of powering the nanobot that allows it to move freely.

The walker consists of two connected feet, each made of a short sequence of DNA bases that attach to a complementary sequence on the DNA track. However, the sequence of bases on the track is designed so that the feet have to compete for a foothold. That means that as one foot steps down, the other is forced to lift off.

The power for this process is supplied by molecules floating nearby, which react together to release energy as long as a specific catalyst is there. The clever part of the design is that the DNA feet themselves act as the catalyst when they lift off the track.

The new walker is designed so that only the back foot can lift at any one time. The walker can put its foot back in the same place or move it forwards but it cannot take a backward step. This also ensures that one foot is always attached to the track.

This design solves some long-standing problems with walking molecules. In some designs, both feet can become detached at the same time, allowing the walker to float away; in others, the feet are just as likely to step backwards as forwards and so end up going nowhere.

There are challenges ahead, however. One is that the DNA track easily gets tangled, preventing the walker from moving. "At the moment, the nanobot has taken a single step but our ambition is to make it move 100 nanometres or more," says Andrew Turberfield, a physicist at the University of Oxford who led the research. To do that, the team will have to find a way to straighten the tracks.

So what else could the nanobot be coaxed into doing? "We can already stop and start our motor by controlling the amount of fuel we add, but we could add other control signals to make walkers interact with each other, and could easily attach a cargo to the region that links the two legs."

We could easily attach cargo to the region that links the nanobot's legs

Niles Pierce from the California Institute of Technology in Pasadena believes the mechanism could significantly outperform previous designs.

Source: University of Oxford /... http://www.nano.org.uk/news/jan2009/latest1736.htm
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« Reply #25 on: August 29, 2009, 09:19:23 PM »



I don't even want to think about where all this is taking us ... but it can't be good.
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« Reply #26 on: August 29, 2009, 09:33:35 PM »


I don't even want to think about where all this is taking us ... but it can't be good.

Yes, and this is one small part of things that "they" are make public...what "they" have in backyard is what can't be good.

As Monkeypox posted "I wonder how many types of nanobacterial they'll be putting in the flu vaccines?"
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« Reply #27 on: September 01, 2009, 02:08:29 PM »

One thing to look at is COST. I would think that for vaccines it would be rather expensive. Unless they can get the victim to pay for the bullet...

On the other hand if the they can disperse a small amount that replicates on it's own, they may very well release them as a controlled side test.. with specific genetic targeting?
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« Reply #28 on: November 06, 2009, 10:42:27 PM »

Nanoparticles could damage DNA at a distance, study suggests

Alok Jha
The Guardian
Fri, 06 Nov 2009 18:27 EST
http://www.guardian.co.uk/science/2009/nov/06/nanoparticles-dna-damage


Nanoparticles of metal can damage the DNA inside cells even if there is no direct contact between them, scientists have found. The discovery provides an insight into how the particles might exert their influence inside the body and points to possible new ways to deliver medical treatments.

The preliminary work also raises questions about the safety of nanoparticles - which are a thousand times smaller than the width of a human hair and used in everything from sunscreens to electronics - though the researchers point out that the doses they used in their study were higher than anything a person might come into contact with.

They also said it was difficult to extrapolate results from their laboratory tests to the human body.

In the experiment, scientists from the University of Bristol grew a layer of cells and exposed one side to cobalt-chromium nanoparticles. On the other side of this cellular barrier were human cells called fibroblasts. Though the nanoparticles never crossed the cellular barrier, they managed to damage the DNA of the fibrolasts via a cascade of biological signals in the intervening cells.

"We imagined a possibility that, in some way, that material had caused a change in the top cell layer and maybe there's some sort of signalling going on from the top cell to the middle cell to the bottom cell," said Patrick Case of the University of Bristol, who led the work.

Case's team found that the DNA in the fibrolasts had around 10 times as much damage, in terms of breaks in the genetic material, compared with control conditions. DNA damage can lead to various diseases, including cancer, but Case said the changes observed in his experiments did not lead him to believe the fibrolasts were becoming cancerous.

The research team deliberately exposed the barrier cells in their experiment to a dose of nanoparticles thousands of times higher than anything that would occur naturally. "We used high doses of them because we wanted to make sure that the dose we used would cause damage to cells if the cells were exposed. When we measured the damage on the other side of the barrier, to our great surprise, not only did we see damage on the other side of the barrier but we saw as much damage as if we'd not had the barrier at all and had put the materials in contact with the cells underneath."

The results were published yesterday http://www.nature.com/nnano/journal/vaop/ncurrent/abs/nnano.2009.313.html in the journal Nature Nanotechnology.

Ashley Blom, head of orthopaedic surgery at the University of Bristol, said: "This work has raised some really interesting questions and given us insight into how barriers in the body might work. The body has lots of different barriers - blood-brain barrier, the skin, the lining of the gut , the placenta - and it may be that this mechanism works in some of these barriers.

"The problem is when you start translating lab work into clinical work. It never works out in the human body like it does in lab-based experiments."

He said that the human body may contain other barriers and mechanisms that scientists still do not understand and which may counteract or enhance the mechanism found by Case. "So I'm cautious in extrapolating this to the human body. But if barriers in the human body do work in this way, the first exciting thing is, can we deliver novel therapies across barriers without having to cross them?"

This would mean that a condition that affects the brain could be treated with something that does not cross the blood-brain barrier and does not come into contact with the brain. "There are wonderful implications for treatments using nanotechnology."

The research also has implications for natural nanoparticles already in human bodies, which might act across membranes to trigger diseases. "Maybe small particles like prions and viruses may utilise some of these mechanisms," said Blom.
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