Synthesizing nanodevices with MONO-ATOMIC GOLD and Human DNA: NANO-DEVICE SELF-ASSEMBLY/ HYBRID HUMAN DNA/ MONO-ATOMIC GOLD and Human DNA: WHERE ARE WE GOING TO END UP IF WE DO NOT REALIZE WE ARE NO LONGER IN CHARGE OF OUR PLANET NOR OUR DESTINY?

Synthesizing nanodevices with MONO-ATOMIC GOLD and Human DNA: NANO-DEVICE SELF-ASSEMBLY/ HYBRID HUMAN DNA/ MONO-ATOMIC GOLD and Human DNA: WHERE ARE WE GOING TO END UP IF WE DO NOT REALIZE WE ARE NO LONGER IN CHARGE OF OUR PLANET NOR OUR DESTINY?

What is the TRUTH about this substance and the effects it has on human psyche, Mind, Brain, Body, Spirituality, and, most importantly, human health? How is it being used against humanity when it may be used for good?

Taken from an article posted on:
http://educate-yourself.org/cn/monoatomicgoldthinktwice15aug05.shtml

  The ability to assemble nano-particles into arrays, networks, and circuits in a precise and controlled manner is key to the fabrication of a variety of nano-devices.

Networks of nanometer-sized metal or semiconductor islands, or quantum dots, may exhibit a variety of quantum phenomena, with applications in optical devices, nanometer-sized sensors, advanced computer architectures, ultra dense memories, and quantum-information science and technology.

Fig. 1
Fig. 1: Typical products of the reaction between DNA and gold particles.

AFM images of thioctic acid-coated gold nano-particles bound to ligated DNA on a mica substrate. The challenge is that fabrication with nano-scale precision of nano-particle arrays in a time and cost effective manner remains a formidable task.

Interest in the concept of self-assembled nano-structures led to the idea of using DNA as a scaffold or template for the programmed assembly of nano-scale arrays.

DNA can be modified with functional groups at predetermined sites to allow for the attachment of other molecules in a specific manner.

We have designed and demonstrated a new approach for binding nano-particles to DNA.

Functionalized nano-particles are covalently bound to internal, chemically modified bases on double-stranded DNA without the presence of destabilizing “nicks” along the DNA backbone.

In addition, we report an approach for thiolating one end of the DNA/nano-particle product and attaching it to a gold surface.

The ability to attach one or both ends of the DNA/gold complex, after generation of the desired pattern, to fixed contacts or electrodes is necessary for nano-device fabrication.

 

Fig. 2

Fig. 2: Close-up of DNA bound to gold particles.

For AFM imaging, the DNA was ligated to produce longer molecules that would be easier to image.

 

DNA oligonucleotides were designed with amino-modified bases for attachment to carboxylic acid functionalized gold particles.

Two double-stranded DNA sequences were used for binding nano-particles.

Sequence 1 DNA was 22 base pairs long with two binding sites for gold per DNA molecule.   The separation between gold binding sites was 3.7 nm.

Sequence 2 DNA was 30 base pairs long, had one gold binding site per DNA molecule, and, after ligation, a 10.5 nm separation between binding sites.

Gold nano-particles with two different passivating coatings were tested. Particles with an average diameter of 1.5 nm were synthesized with a mercaptosuccinic acid coating, and particles approximately 2.5 nm in size were coated with thioctic acid

Each particle has multiple reactive carboxyl groups on its surface. In order to decrease the probability for one particle binding to many amino groups on the DNA, methyl-amine was used to block some of the carboxyl groups on the gold. Methyl-amine was chosen for this purpose because of its small size and similarity to the methylene side chain containing the amino group on the DNA.

The reaction between the amino group on the DNA and the carboxyl group on the gold particle was facilitated using a standard chemical method for joining carboxyl groups to amino groups.

Analysis of the products by gel electrophoresis and atomic force microscopy (AFM) showed the gold particles bound to the DNA.

In addition, absorbance spectra of the gold nano-particles in the presence of DNA provide evidence of binding.

This technique addresses a basic need to assemble nanometer-scale objects in a programmable manner and in a parallel fashion, from the bottom up.

 

Research by K. A. Stevenson, G. Muralidharan, L. Maya, J. C. Wells, J. Barhen, and T.G. Thundat, Center for Engineering Science Advanced Research, ORNL; for details see “Covalent Attachement of Gold Nanoparticles to DNA Templates”, J. Nanosci. Nanotech (submitted, 2002).

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Authors notes:

Since this was written in 2002, there has been a great deal of work on nano-materials and how to synthesize nanodevices using atomic and/or molecular scavenging of biological material to “stockpile” the required “feed-stocks” for self-assembly of any pre-programmed nano-scale electronic/biological based systems we care to design.

Our understanding of design and fabrication of the required material physics we would use to design and produce almost any conceivable electromagnetic, electronic, or mechanical components and systems within living biological systems (read HUMAN)  

DARPA and others have developed a new form of synthetic micro-biology: an organism that is NOT ALIVE, yet functions as though it were alive.

This allows the organism to do almost any job you can design. It may be operated via DNA/GNA instruction sets pre-programmed, as well as outside control offered by electromagnetic/electrostatic/scalar energy manipulation, as well as through chemical means.

It can not be KILLED if it was NEVER ALIVE in the first place.

This is a sophisticated nano-biological system capable of existing in almost any environment, able to lay “dormant” conceivably forever, able to infect any living organism and reproduce itself like any virus.

Able to carry out its instruction set (say, scavenge molecules/atoms from the cells and create a network or bio-sensors, optical sensors, neural interconnect sensors, energy transducers, radio-telemetry, tracking and unique identifier systems, piezoelectric crystals, metal micro coils, semiconductors, capacitors, resistors, diodes, and more,) and they lay dormant inside the living ‘host’ organism.

Dormant only until the proper frequency and energy signature electromagnetic wave is transmitted across the planet by H.A.A.R.P. and E.I.S.C.A.T. and G.W.E.N. and cellular systems, bringing the organism out of stasis and causing it to replicate uncontrollably, thus destroying the ‘host’ in the same way cancer would.

Combine this with the ultra sophisticated quantum computers hosting Artificial Intelligence that would be used to monitor and control this network of modified biological beings.

With the ability to read thoughts, model behavior, change emotions, entrain brain states, create virtual reality for the experiencer, send audio messages to the recipient that only they can hear, ability to interface with the human mind and read the dreams, hopes, fears, and private ideas of every single living being on the planet.

It can broadcast thoughts and ideas directly into your brain, and it can talk to you in a voice you think is your own inner voice.

So HOW COULD YOU TELL IT APART FROM YOUR OWN THOUGHTS?

This is where we are going.

Morgellons already infects the entire human population (at least 75%)

How many targeted individuals realize they are being tortured with this exact technology?

How many innocent people do not yet realize what is being done to them?

How many of us can even fully understand the science-fiction like reality that we are being drawn into without our consent?

Please, humanity, if you believe that we deserve to continue to exist as a species, then we MUST wake up and act as one under love with compassion to change this world back into the paradise it was originally before we allowed humans to destroy it.

 Thank you for your time and interest.

I hope you will look deep with in your self for THIS is where we must FIRST CHANGE in order to CHANGE our WORLD for the best!

Blessings and peace.

Timothy Trespas