|
Post by skytroll on Jun 7, 2007 8:40:57 GMT -5
oH BIOLOGY AND NANO TOGETHER AT LAST! "Bionanotechnology: Viruses may help build nanodevices. Paraphrased from U.S.News & World Report, Science & Society 1/12/2004, pages 46-47, by Karen Schmidt. Angela Belcher a materials scientist at the Massachusetts Institute of Technology has manufactured semiconductor materials into circuits less than a hundredth the size of devices on a standard microchip using viruses. Her team has developed harmless viruses that can bind and handle 30 different materials, as well as possibly grow wires for some of the world's tiniest transistors. Measured in nanometers, or one billionth of a meter--the length of 10 hydrogen atoms lined up in a row, nanodevices could form the heart of superdense computer chips, more efficient solar cells, and perhaps even tiny factories. And living cells may help construct them. After all, life's molecules are masters at building nanomachines, from the molecular motors in muscle to the tiny cellular power plants that extract energy from food. The idea is to exploit biology's assembly skills to build new nanodevices. Instead of domesticating plants and animals, it's time to domesticate molecules according to the burgeoning field of bionanotechnology. Biology may be able to design nanodevices that build themselves, from the bottom up. Susan Lindquist, Director of MIT’s Whitehead Institute for Biomedical research, is trying to do just that with the help of aberrant proteins called prions. Protein molecules normally fold up like origami into a shape that enables them to do their job, but in prions, the folding somehow goes wrong. Prions are notorious as the cause of fatal brain ailments like mad cow disease , but Lindquist discovered that one kind of prion--from yeast--can do something potentially useful. She triggered a chain reaction in which the yeast prions spin themselves into long, durable fibers. Lindquist then genetically engineered these fibrous prions so they could bind to gold and silver nanoparticles. As she reported in spring of 2003, the result was prion fibers clad in precious metal--ultrafine conductive wires that could someday shuttle electrons around nano-size circuits." SEE THE THE GOLD PARTICLED TIP ON THIS AND OTHER CONSTRUCTIONS: tinyurl.com/2dyknnsince when you go on above link it changes, here is the exact link: fig.cox.miami.edu/~cmallery/255/255trends/bionanotechnology.htmIF ON THE INTERNET IF DOCMENTED IS FREEDOM OF INFO> I have a right! SKYTROLL
|
|
|
Post by skytroll on Jun 7, 2007 8:59:04 GMT -5
|
|
|
Post by skytroll on Jun 7, 2007 9:05:05 GMT -5
|
|
|
Post by whiterose on Jun 9, 2007 8:41:07 GMT -5
Dr. Hildegarde Staninger discussed some folks having different letters of the alphabet at different joints, makes you wonder if the joints aren't being labeled. What do you think?
|
|
|
Post by brimstone on Jun 9, 2007 19:23:43 GMT -5
With respect to the research of Dr. Susan Lindquist: AmyloidosisSome of us may be genetically disposed for protein misfolding in excess of the normal misfolding scope. Or some of us have been more exposed to elements that are known to set off or enhance protein misfolding, for example a) indistcriminate use of antibiotics (opening the way for overgrowth of fungus and virus and bacteria that are not targeted by the applied antibiotic, f.ex. e-coli which in itself is a proven cause/accellerator of protein misfolding) b) certain forms of anaesthetics known to penetrate proteins and cause misfolding Different proteins or prions are involved and express themselves in somewhat different illnesses: Alzheimers, Parkinson, Mad Cow disease - and for Morgellons sufferers, may be: Cutaneous Amyloidosis. Amyloidosis is often connected to transthyretin misfolding which in turn is connected to the production of thyroid hormones. Hypothyroidism is therefore often a marker of existing or potential amyloidosis. Yeast infections, certainly candidiasis, are known to cause hypothyroidism. Amyloid proteins attract and protect microbial constellations (bacteria, fungus, virus, mycoplasma - biofilm), thus providing shelter from the body's normal immune reactions. The "melange", turns into a veritable assembly line - picking up the nano-particled minerals and chemicals in the body and working them into fibers, clots/lumps and plaques. Amyloid fibers/tissues are fluorescent - typically orange. (Could colours and patterns vary according to microbial constellations?) Dr. Susan Lindquist, has (also) discovered that another protein, the Hsp104, plays a role in the misfolding process: None (or very little) of it is good (no amyloids) and large amounts of it is good (actually dissolves amyloids). Amounts inbetween appear to accelerate the misfolding process. Hsp104 is produced by fungi - in particular saccharomyces cerevisiae - sugar yeast (= baker's yeast). The amyloid (nano-)assembly line seems to be indiscriminate and uses any mineral or chemical that comes along, like calcium, natrium, potassium, zink, copper, fats etc. which are deacetylised and/or oxydised. (Which all seems to be in line with Dr. Staninger's findings.) The produce seems to get stacked into colloid and/or cytoid cells (or bodies) within in the human body and cause damage. Cutanous amyloidosis is apparently not an affliction of the skin only - but can be generalised. Amyloids will retain/release water and therefore cause comings and goings of swellings or plumpness. The renewal of the body - entailing both normal and abnormal proteinfolding - is a cyclic phenomenon. For those interested in researching this angle further: Some key words to google: Amyloids, amyloid proteins, amyloid fibers (or fibrils), amyloid fiber images, cutaneous amyloidosis, protein (mis-)folding, colloid cells, cytoid cells, prions, sup35, Hsp104, role of e-coli in protein folding, metals and amyloids, transthyretin, biofilm. I also recommend researching "excitotoxins" - and this is an interesting read: www.dorway.com/blayenn.html
|
|
|
Post by skytroll on Jun 9, 2007 23:26:59 GMT -5
Excellent! Been trying to say this. The amyloid fibers are not only in the brain. Proteins are caused to misfold by use of the prion of S. Cereviscaea. see the other link on the bacteriophage, that is the way in replaces antibiotics, the virus remains......can be latent, when immune system goes down, it waits....and it attacks. One needs to go back and look at when they started to be infiltrated into drugs without our knowing it, when infiltrated into foods, into nanotubes for use in aerosol operations, as a way to save the earth? from global warming? Right! There is a plan: We are in this phase now: www.metabolicengineering.gov/five_year_plan2.htmkeep at it folks, there is more than one thing going on, that is why we have different stages, different symtoms, and yet all the same DNA is being altered in us, if it is done in plants, animals, the earth, why would it not be done in us? All about Adaptation to the new climate change engineered by? Skytroll Skytroll
|
|
|
Post by skytroll on Jun 9, 2007 23:28:19 GMT -5
|
|
|
Post by skytroll on Jun 10, 2007 14:32:56 GMT -5
you are welcome,
s
|
|
|
Post by brimstone on Jun 10, 2007 15:56:45 GMT -5
Amyloidosis, continuedPutting the original causative agent for this disease (be it chemtrails, GM's, protozoans, bryozoans, efforts to kill off people with certain blood groups or personalities, agent XYZ, government control implants or superbugs of some or any form) on hold for just a second, I believe every Morgellons sufferer would be well served (both mentally and financially) by obtaining a diagnosis that doctors, insurance companies and health care systems can relate to. Amyloidosis is metabolic illness and a known condition which the powers that be are taking seriously. It is easy to diagnose with a biopsy, provided one knows where the amyloid deposits are located and can extract them. Biopsying a person with symptoms of dementia or CNS-problems, but no visible or palpable deposits, is not practical and is not done. That the cause in these cases indeed is misfolded protein deposits, is mostly only ascertained post mortem. But lucky me - I can point them out. When I presented the proposition of cutaneous amyloidosis together with an imagage of what a slice of "colloid cutaneous amyloidosis" looks like to my GP, he instantly recognised the spikes (sliced through) and the egg-like lumps that become visible when the skin ruptures. He sat back and said "wow - yes - very likely. dermatlas.med.jhmi.edu/derm/IndexDisplay.cfm?ImageID=-171698588As you will observe if you do some research, there is not much that isn't known about proteins and proteinfolding (or misfolding) on the biologists' level. Little, however, seems to have rippled through to the medical profession in general. Actually it seems that veterinarians know more on this subject than MD's do. My GP knew that "amyloid" had something to do with Alzheimers and Parkinsons, but had no idea that it could be cutanoeus (or affect any which organ for that matter). He started reading up on the subject. He also shares my general opinion that dermatologists should be refunded for long tuitions to no awail, so he decided to do a thorough write up himself on what, why and how and send me to a general surgeon for the biopsy. Appointment end of July. If I am correctBeing diagnosed with Amyloidosis has, of course, limited value in as much as there isn't any "fix" out there, and what really causes these types of illnesses is still anybody's guess. If it really is amyloidosis, I am also glad I didn't find out before, as I would not have been on the present medication (antimicrobial) then, but rather on hormones, steroids/NSAID's and antihistamines - like everybody else diagnosed with "auto immune"-diseases. If I am not correctNo worse off than before
|
|
|
Post by skytroll on Jun 13, 2007 13:24:06 GMT -5
G-wire, a new DNA nanostructure, Could this be the connect to the Barium, Calcium, and Magnesium involved in Chemtrail drops? www.pubmedcentral.nih.gov/articlerender.fcgi?artid=306740G4-DNA: We are talking quad strand DNA, 4 strand, not two strand, the usual human being. nar.oxfordjournals.org/cgi/content/full/31/4/1156/GKG211F5worm-chip.stanford.edu/telomeres_pubmed.1989.htmlwww.uga.edu/~protozoa/portal/stich_molec_bio.htmlwww.genesdev.org/cgi/content/full/19/1/77trophort.com/011/407/011407012.html"ATP synthesis from ADP, Pi, and Mg2+ takes place in mitochondria on the catalytic F1 unit (33) of the ATP synthase complex (F0F1), a remarkable nanomachine that interconverts electrochemical and mechanical energy, producing the high energy terminal bond of ATP." www.jbc.org/cgi/content/full/281/19/13777#REF13ATP synthesis? more later RNA meets chromatin? skytroll www.euchromatin.com/Bernstein01.htm
|
|
|
Post by skytroll on Jun 13, 2007 13:29:54 GMT -5
|
|
|
Post by skytroll on Jun 17, 2007 23:44:30 GMT -5
Where is the real danger? ...."The life sciences are developing so quickly that a watch list of dangerous pathogens and toxins is useless in fighting the threat of bioterrorism, says a new report from the US National Academy of Sciences. The report, on "next generation" bioterrorism, was requested by the US government. It concludes that intelligence agencies are too focused on specific lists of bacteria and viruses, and are not aware of emerging threats. Focusing on the list of about 60 "select agents", such as the smallpox virus and botulism toxin, might simply divert resources from newer and more dangerous threats, such as RNA interference, synthetic biology or nanotechnology. Our report "pushes back against the monomaniacal focus on bacteria, against the idea that if you can write a list of bad bacteria and control them then you're okay," says Peter A Singer, a bioethicist at the University of Toronto, Canada, who was on the NAS report committee. As examples, the report suggests it might soon be possible to engineer a virulent pathogen from scratch using DNA synthesis and that advances in gene therapy might make it possible to release an aerosol of a harmful gene that would be inhaled by victims. ....."The best defence, according to the report, is for the US to encourage a free flow of information among international scientists while also setting up international agreements that prohibit work intended specifically for biological weapons. In the shorter term, the US should set up a special committee to monitor scientific developments and report to intelligence agencies, the report says." link: www.newscientist.com/article.ns?id=dn8656skytroll
|
|
|
Post by sarahconnor on Jun 17, 2007 23:55:14 GMT -5
What a great idea.
|
|
|
Post by skytroll on Jun 18, 2007 2:00:41 GMT -5
Brimstone,
Thanks for the info on amyloid
Sarahconnor,
good to hear from you. Yes, I was thinking the same thing.
In that article they talk of nano being more a danger that bioweapons. I think they are right.
......................
In the article above it mentions how nano technology may be worse than bioweapons.
I found this and am quite surprised that nanobes, another name for nanotubes is what we are dealing with.
Even the singularity folks warn of release of these.
And yet no one monitoring this, I thought that is what the Investigators did?
Some clues?"dear Shane, You write: "....but I think more work in to the recently discovered nanobes from deep sediments might be more crucial." So I checked the claims about nanobes. If you have a look in biological scientific literature "nanobes" do not get a single hit (try NCBI homepage search program). This clearly demonstrates that they are not considered to be organisms. Furthermore I've read the article by Phillipa Uwins et al (American Minarologist, volume 83, p1541-1550.) The authors claim a lot. 1) nanobes grow = unwarranted conclusion. Probably it is nothing but crystalisation/polymerisation, 2) nanobes have a heterotrophic metabolism = unwarranted conclusion. polymerisation requires monomers from their environment, 3) nanobes resemble actinomycetes and fungi = so what, there are piles of rock on Mars that resemble a face, 4) nanobes are composed of C, O, and N and that is consistent with living matter = unwarrented conclusion. The atmosphere is also composed of C, O and N. 5) nanobes appear to be membrane bound structures, a cytoplasma and nuclear area = unwarranted conclusion. All they show is that nanobes are morhological distinct microvessels. 6) nanobes have amorphic wall structres = sowhat. Stones have amorphic wall structures. 7) nanobes contain DNA as indicated by DAPI, Acridine orange and Feulgen staining = unwarranted conclusion. The nanobes may stain aspecificly. They did not include negative controls. They did not isolate DNA (very simple procedure). My conclusion: this article is a hoax. If it really had been something it would have been published in Nature, Science or other leading scientific journal. Don't believe the hype! best wishes, Peter -------------------------------------------------------------------------------- This message is a reply to: Message 15 by singularity, posted 07-26-2002 04:37 AM -------------------------------------------------------------------------------- Replies to this message: Message 29 by singularity, posted 07-30-2002 12:58 AM -------------------------------------------------------------------------------- -------------------------------------------------------------------------------- Hi Peter I will admit to not knowing the full background of the stone age malaysian tribe story- it was more to illustrate the point that all societies seem to need some story of their ultimate origin (being a hoax fits this suggestion). We are all compelled to take sides in this debate to varying degrees." from this forum: www.evcforum.net/cgi-bin/dm.cgi?action=msg&f=13&t=6&m=16Molecular assemblers: www.molecularassembler.com/KSRM/Refs2600-2699.htmSo, I will check this out, for sure. on the Morrow!
Skytroll
|
|
|
Post by skytroll on Jun 18, 2007 14:10:17 GMT -5
|
|
|
Post by skytroll on Jun 18, 2007 14:12:57 GMT -5
|
|
|
Post by skytroll on Jun 18, 2007 14:36:25 GMT -5
|
|
|
Post by skytroll on Jun 18, 2007 22:57:43 GMT -5
|
|
|
Post by skytroll on Jun 19, 2007 23:33:23 GMT -5
By presidential order this was put in place and involves the wetlands, the algae etc. www.ostp.gov/Environment/html/teamingcover.htmland there is much more: "New pharmaceuticals. Drugs derived from the world’s species save countless lives and generate many billions of dollars in sales worldwide. Most of the species within those groups of organisms that have the greatest potential to provide new sources of medicines have yet to be discovered or described. For example, bacteria are diverse and constitute a major source of new pharmaceuticals and other biotechnology products. The better their diversity, and that of many other groups of organisms, is understood, the more likely it is that we will discover useful genes and gene products, and their functioning and interactions"www.ostp.gov/Environment/html/teamingsec2.htmlquite a group wouldn't you say? "To make these advances possible, it will be necessary to expand support for ecological and ecosystem research in academic and other institutions. It will also be necessary to increase the size of the nation’s system of permanent research sites at which the environment is observed; experimental, comparative and synthetic research is conducted; and predictive models are generated and tested. The Long Term Ecological Research network of sites, currently incorporating 20 research areas, should be increased to more thoroughly cover the range of America’s ecosystems (especially important to add are the full range of marine ecosystems from coral reefs and major fisheries to the open oceans). Additional areas, for example national parks or Man and the Biosphere reserves, should be established as centers for the types of research described here. The nature of this research will also require an increase in the number of monitoring and research sites maintained by agencies such as the EPA, NOAA, the Department of Energy, the US Forest Service, and the USGS/BRD. Also, assurance of access for researchers to Mission to Planet Earth and Landsat data and data processing are important to this effort. A number of agencies already have a stake in the support facilities needed for this research, including NOAA, the Forest Service, the USGS, the EPA, the Department of Energy, and the NSF. Current investments (approximately $300 million per year, spread across the several listed agencies) should be enhanced by approximately $55 million per year in order to increase the return on this investment, with the greatest additions made to programs that use rigorous peer review. Infrastructure capacity and performance by Federal agencies that already have research and monitoring sites in place should be increased immediately; the remainder of the increases should be accomplished within three to five years. "Has this all been fulfilled? pretty close I'd say. 1998? skytroll
|
|
|
Post by skytroll on Jun 19, 2007 23:45:14 GMT -5
"The preparation of this report was supported by a partnership among The George Gund Foundation, The John D. and Catherine T. MacArthur Foundation, IBM, Lucent Technologies, the National Science Foundation, the Environmenal Protection Agency, and the National Aeronautics and Space Administration. " www.ostp.gov/Environment/html/teamingsec5.htmlMore on the secret work done during that administration which brought about all the tech we have today, and they knew nothing of nanotech? Right! Skytroll
|
|
|
Post by skytroll on Jun 19, 2007 23:55:06 GMT -5
Here is something interesting: www.ecotality.com/blog/2007/driving-the-wrong-way/"Between 1978 and 1996, the Department of Energy (DOE) funded research into technologies that could have significant impacts on the consumption of fossil fuels. The focus of this research became the Aquatic Species Program (ASP), which investigated renewable fuel production (biodiesel) from high-oil algae species, fed by the waste CO2 from coal-fired plants. Researchers whittled down over 3,000 strains of microorganisms into the most productive 300, and constructed 1000 sq. meter test ponds outside of Roswell, NM. The ponds were set up as sort of algae ‘race-tracks’, where algae were circulated around shallow, oval-shaped ponds as carbon dioxide bubbled through the mixture. Results were successful and encouraging, but the program fizzled out after almost 2 decades (a lot of which had to do with a budget crunch and allocating more resources to researching ethanol). Researchers noted that one obstacle to large-scale algae production may be the high cost, which was estimated to be double the price of diesel at the time. (I wonder what they would say now.) Utah State may finally take this research to the next level. Scientists there plan to produce algae in a grid of indoor bioreactors, with light captured by parabolic dishes on the roof and fed inside via fiber-optic cables. Put several thousand of these bioreactors together and you have an algae farm:" www.ecotality.com/blog/2007/algae-biodiesel-may-soon-be-reality/am onto this, won't stop till I find the "crobe" Don't forget the midge as vector of the cyano laced microbes. skytroll
|
|
|
Post by whiterose on Jun 21, 2007 17:32:08 GMT -5
|
|
|
Post by sarahconnor on Jun 21, 2007 19:42:08 GMT -5
YOU BET I DO!
|
|
|
Post by whiterose on Jun 21, 2007 20:15:32 GMT -5
If you want a real eye opener type in CDC or NSA or DOE or DOD and there are others but I don't wish to bore you, but remember to put up a plus sign and the word nanotechnology! i.e., CDC + nanotechnology We also have posted under nano discussion Dave Larsons work, some really cool pictures that look just like what a lot of us have found! morgellonsgroup.proboards23.com/index.cgi?board=alter&action=display&thread=1169050966Than there is all of Dr. Hildegarde Staningers work and the Morgellons links at the left hand side of the www.rense.com page.
|
|
|
Post by whiterose on Jun 21, 2007 20:21:43 GMT -5
|
|
|
Post by sarahconnor on Jun 21, 2007 21:06:21 GMT -5
sick.
|
|
|
Post by skytroll on Jun 21, 2007 22:34:21 GMT -5
|
|
|
Post by skytroll on Jun 21, 2007 22:49:14 GMT -5
|
|
|
Post by skytroll on Jun 21, 2007 23:19:56 GMT -5
|
|
|
Post by whiterose on Jun 22, 2007 21:15:06 GMT -5
This and the previous post are on page 2, go to page 1 for the rest of the line of well thought out posts, in case your new here, always check the page number once you get into the link, that way you don't miss all the good stuff!
wr
|
|