DNA DISRUPTION IN
VIRUSES AND ANIMALS
BY THE USE OF SPECIFIC FREQUENCIES OF
ELECTROMAGNETIC RADIATION WHICH MATCH THE RESONANCE FREQUENCIES OF THE DNA
SECTION WHEN THE DNA SECTION IS CONSIDERED AS AN ELECTRICALLY CONDUCTIVE
ANTENNA STRUCTURE
By
OVERVIEW
FOR THE LAYMAN - In this article the fact that the most common form of DNA (
B-DNA) is electrically conductive is used to show that viral, bacterial, and
animal (human) DNA can be thought of and used as tuned "radio" antennas.
For example by choosing the proper frequency of light to match a resonance
frequency of the length of DNA in a virus, the oscillating electric field of
the light can induce an electric current from the virus DNA ends (field
emission). This field emission can damage the virus DNA end segments and
surrounding protein structures and thereby make the virus non-infective. When
considering human DNA gene sets as tuned antenna, specific frequencies in the
microwave range can be used at relatively low power levels for short time
intervals to open up specific gene sets. This allows for resetting of genetic
age clocks (restoring telomeres on chromosome ends), reversal of some genetic
defects, and total tissue repair (opening up some fetal gene sequences), even
from traumatic damage such as amputations and brain and spinal cord damage.
(Note: you can now print out the figures in Landscape mode--Ed 1/30)
THE TECHNICAL DETAILS
DNA when it is in the B–DNA form, the DNA form
normally found in abundance in plants and animals, is known to be an electrical
conductor along its core. It is not as good a conductor as a metal, more
comparable to that of a semi-conductor or conductive polymer (ref. 1,2,3). This
electrical conductivity allows us to consider a B–DNA strand of a fixed length
as a "tuned" antenna. The length of the viral DNA is rather short,
the great majority ranging from around 2,000 to 200,000 DNA base pairs in
length, depending on the particular virus under consideration. Figure 1A illustrates a graphically linearized version
of a very simple DNA virus, where the DNA length S has been chosen as the half
wavelength (S = 1/2 Y) resonant antenna for an applied oscillating
electromagnetic field of frequency (F). Figure 1B shows a more realistic graphical
illustration of this simple virus where the DNA strand of length S is complexed
with a protein coat in the form of a coil. The coiled DNA has both inductance
and capacitance that will effect the resonant frequency and wave speed of/on
the DNA coil. However, for our purposes the coiled B-DNA to a first
approximation acts electrically essentially like a straight antenna of length S
as depicted in Figure 1A. For our purposes, since the (LC) resonance
phenomenon does not reduce the field emission, but only shifts the frequency at
which it occurs at most efficiently, we will therefore ignore the inductance
and capacitance of the virus coiled DNA. The applied resonant electric field
(specific frequency of light), if of high enough intensity, will drive the DNA
core electrons back and forth to a voltage / electric field amplitude at the
DNA strand ends, such that electrons are emitted at the ends of the DNA by a
process similar to the well known phenomenon of field emission from the surface
of a metal point.
Field emission from a metal point is a very
non-linear process in terms of the electric field (goes as the square of the
electric field) and the electric field is approximately proportional to the
inverse fourth power of the radius of curvature of the point of emission. The
radius of curvature of the DNA conductive core is only ~ 3 angstroms and a
relatively modest applied electromagnetic field intensity should, in a
resonance situation, induce large amplitude electric fields at the DNA strand
ends. Since the DNA core has a much lower density of conduction electrons than
a metal core would have, the field emission probability of the emission
(quantum tunneling) of an electron approaching the DNA strand end should
significantly increase because there will be a greatly reduced image charge
potential barrier. From these conditions we can surmise the strong possibility
of substantial electron field emission from DNA strand ends under the above
stated conditions. Furthermore, if these emitted electrons have acquired enough
kinetic energy they can denature and/or destroy the chemical bonds of DNA
coating proteins as well as disrupting any chemical structure in the local
area. Also, in this protein damaging process, damage to the end DNA base pairs
can be expected. In other words, a DNA strand exposed to its resonant
electromagnetic frequency at adequate intensity should in short order become
non-functional as a viable virus DNA to infect a host. This proposed phenomenon
lends great support to some forms of light or color therapy, which have been
persecuted by orthodox pharmaceutical driven allopathic medicine for eighty
plus years now.
Equation 1 is the universal relationship
between wavelength (Y), frequency (F), and wave propagation velocity (V) for
all wave phenomenon.
V = Y F ; Equation 1.
For some wave phenomena V is frequency dependent.
However, in our interested area it should be a near constant value. Considering
the DNA strand of Figure 1A as a half wave antenna (S = Y/2) and putting Y in
terms of S into equation 1 we obtain:
F = ( V ) / 2S ; Equation 2.
The DNA strand of Figure 1A could just as
well have been considered as a full wave antenna (Y = S), a three half wave
antenna ( Y = 2S / 3 ), a two wave antenna ( Y = S / 2 ), etc.. Equation 2 is a
special case of the general equation describing the possible resonance frequencies
that the DNA antenna can support, namely Equation 3.
F = NV / 2S ; where N = 1,2,3, … Equation 3.
Figures 2 A, B, C, and
D illustrates N = 1, 2, 3, and 4 of equation 3, where the curves represent
the boundary envelope for the maximum value that the oscillating voltage
reaches at each point along the DNA strand. For example, consider the point C
on the DNA strand of Figure 2A. In Figure 3, the
voltage point C is plotted verses time for the situation depicted in Figure 2A. The
plot of the voltage verses time for any point along the DNA strand looks like Figure 3, except
the maximum amplitude varies from point to point. The voltage at a point on the
DNA in one envelope oscillates 180 degrees out of phase with the voltage at a
point in the adjacent envelope. If the DNA strand of Figures 2A, B, C, and D
are exposed to "light" frequencies, which are somewhat off the
resonance frequencies given by Equation 3, standing waves will still be formed
on the DNA strand similar to those illustrated in Figures 2A, B, C, and D.
However, the maximum voltage amplitude on the DNA ends will decrease
significantly with increasing frequency shift off the resonance frequencies.
The virus
illustrated in Figures
1A and Figure B
are very simple and do not have the commonly observed lipid covered protein
capsid coat of many common viruses that infect animals and plants. Just such a
common virus is illustrated in Figure 4. The
virus of Figure 4 looks a great deal different than the virus of Figure 1.
However, to a first approximation it is only the length of the DNA segment that
is dominate in determining the resonance frequency. The shape of the DNA strand
is not too critical in most cases. An example of a good exception to this would
be a lambda bacteriophage. In the lambda bacteriophage the DNA is very tightly
packed under high compression into a many turned and layered coil which has
significant inductance and capacitance. Also, the electrical conductivity could
be significantly increased do to the high compression of and highly restricted
movement of the lambda DNA in its capsid.
Let us
use Equation 3 and some possibly reasonable values for V, S, and N to obtain
approximate electromagnetic frequency ranges that could disrupt or destroy some
virus. Let our virus of interest have a DNA strand of 20,000 DNA base pairs.
The average length per base pair in B-DNA is 3.4 angstroms (an angstrom equals
ten to the minus ten meters). This implies that the DNA strand length (S) is
6.8 microns. Let us guesstimate that V is .9 the speed of light.
Let N = 1, 2, 3, and 4. Then:
F = N ( 1.98 x 10 exp.13 sec.-1) , Equation
4.
F1 = 1.98 x 10 exp.13 sec.-1
----------------------- Y1 = 15.113 microns
F2 = 3.97 x 10 exp.13 sec.-1
----------------------- Y2 = 7.5565 microns
F3 = 5.95 x 10 exp.13 sec.-1
------------------------ Y3 = 5.0377 microns
F4 = 7.94 x 10 exp.13 sec.-1
----------------------- Y4 = 3.7783 microns
All of these resonance frequencies /
wavelengths are in the infrared band range. If we had chosen a virus of 2,000
DNA base pairs, then the wavelengths would have been ten times smaller.
Y1 = 1.51 microns ( top of infrared band )
Y2 = .7556 microns ( Very top of infrared
band )
Y3 = .5037 microns ( green light )
Y4 = .3778 microns ( bottom of ultraviolet
band )
These
results are potentially rather significant because there are many. many viruses
that have DNA bases pair counts in the 2,000 to 20,000 and beyond range which
cause serious health problems / diseases in people for which we currently have
no viable treatments. We now
have available tunable lasers, which can cover the top of the infrared band
through the visible band into the ultraviolet band. These tunable lasers can be
used to treat the blood directly or can be used in intense pulse scanning mode
to treat the surface tissue and at depth in some cases. It is necessary to use
a relatively narrow band of frequencies (specific color) to efficiently and
effectively destroy the virus. If broad spectra light (i.e. white light) is
used, the conduction electrons in the B-DNA core see the composite random
oscillating electric field from all the different colors (frequencies) and will
not form a strong resonant or near resonant electrical oscillation that is
required to destroy the virus by the method discussed above. There are also
very strong light sources commercially available, which produce frequency bands
from the infrared through the ultraviolet. With appropriate filtering of these
light sources, a viable whole body treatment modality can be envisioned. It is
also conceivable to fire or cook into certain ceramics, certain molecules and
mono atomic elements to obtain narrow band electromagnetic frequency emissions
from the ceramics upon raising them to the appropriate temperature and then
filtering out what is not wanted. It is even conceivable to "filter"
infrared light from a very intense blackbody source to be used in treatment.
What we
have been considering here for treatment on humans can of course be used on
animals and plants in general. We can even imagine protecting one cell plants
and animals as well as bacteria from viral attack by the use of specific
frequencies of electromagnetic fields. Also, we may wish to wonder about
finding the resonant frequencies for the chromosome DNA of certain bacteria. Can
we disrupt or denature the chromosomal and or plasmid DNA of bacteria using
resonant standing wave electromagnetic radiation? For example, imagine a
bacterial plasmid that codes for an enzyme that destroys some anti-biotic. If
this plasmid has a short electrically non-conductive segment such as Z-DNA,
then the above used antenna formula can be used to destroy the plasmid. Imagine
a small room (chamber) where a patient would stand in their nature suit bathed
in all directions by a light as brilliant as the sun, but of only a very narrow
frequency range (a specific color). Thirty seconds in the room and you go home
just fine.
Now that
you are familiar with the concept of various virus DNA lengths being treated as
a tuned antenna, let us extend the concept to the chromosome size scale.
Research has shown that the relaxed chromosome in the cell nucleus can be
considered as a series of genes and gene sets sequences each gene set to be
read all together or not at all. These gene sets are often separated/partitioned
from each other by combinations of promoter and blocker proteins and or Z-DNA
segments. Z-DNA is generally formed and maintained by the interaction between
specific short DNA base pair sequences and certain ion complexes. Z-DNA is not
electrically conductive and acts like an insulator separating two B-DNA
conductors. Z-DNA effectively partitions chromosome B-DNA into a set of tuned
antennas. Furthermore, the proteins that complex to the surface of the
chromosome undoubtedly affect the electrical conductivity of that local B-DNA
base pair sequence or region. In some cases the conductivity may increase and
in others it may decrease. In some cases this B-DNA region may gain significant
resistance even to the point of becoming effectively non-conductive. Also, at
any one moment there are often many B-DNA transcription enzymes at work on a
single chromosome transcribing gene sequences.
The
transcription enzyme splits the DNA at its location into two separate single
DNA base sequence strands during transcription and therefore stops electrical
conductivity at this location. Figures 5 shows a
small section of chromosome which illustrates the situation just described. So,
it should be clear that the chromosomes could be considered as a set of both
isolated and coupled tuned antennas as illustrated in Figure 6, where only the
electrical properties of the chromosome are dwelt upon. The tuned antennas of
the chromosome illustrated in Figure 6 are
generally much longer in length than those of viruses and therefore have
fundamental resonance frequencies considerably lower. Namely in the low
gigahertz range. For example, when the cell phone companies say / claim that
there is no scientific proof that cell phone use is harmful, they lie. It has
been known since the 1960’s that R.F. in the 1 gigahertz range can cause
chromosome damage and breakage. It was originally proposed to use this fact to study
the phenomena of chromosome damage and breakage. The next time you use a cell
phone ask yourself: Do I feel lucky ? Well, do you feel lucky? Well, do you?
There are
potentially great benefits available from exposing animal cells to specific
sets of microwave frequencies for brief time intervals at the appropriate
intensities. Various gene sets can be opened up with phenomenal results. For
example, resetting the telomere " time " clocks in cells giving
people vastly extended youthfulness, reversing genetic diseases, and completely
repairing massive body tissue damage such as spinal cord injuries, brain
injuries, organ damage, and amputations. As bold as the above statements may
seem, their truth or validity is easy to see when you consider a few facts and
observations. First, consider fetal development, the fetus develops out of a
fertilized egg in a totally genetically orchestrated/programmed fashion just
like clockwork. Large numbers of gene sequences are expressed and then shut
down usually not to be expressed again during the individual’s normal lifetime.
Note that fetuses have been operated on in the womb, and when born have no
scaring evident, i.e. complete tissue repair. This ability is shut down
sometime before birth. Just as your development to birth is genetically
programmed, your death is also. As you age with the need for continuous cell
division for tissue repair and maintenance, you loose telomeres on the ends of
each of the chromosomes of the dividing cells. As this process proceeds the length
of the telomeres get shorter and shorter and the cell division rate continually
decreases to the point that health can not be maintained and you die.
Experimentally from tissue regeneration experiments done with salamanders and
rats( Dr. Robert Becker’s work) it is known that amputated limbs of mammals can
be re-grown (ref. 4). That is total tissue regeneration. Cells were made to
become embryonic-like (de-differentiation) and then to multiply and then
differentiate into all the needed body cell types to reform the missing
amputated limb. In this process gene sequences that had been shut down to be
never accessed again were opened up and expressed and apparently the
chromosomes did not initially suffer telomere shorting.
Analyses
of Becker’s work shows that it is the drastic change in the concentration of
positively charged metal ion complexes in the cell cytoplasm surrounding the
chromosomal DNA that causes the dedifferentiation of cell structure (ref. 5).
In the re-growing of rat arms, it was the exposure of the cells at the
amputation site to feeble negative electric currents that formed high hydroxyl
ion concentrations around the amputation site, which attracted the positively
charged metal ions into the region. This high hydroxyl ion concentration brought
in high positive metal ion concentrations to mask the excess negative hydroxyl
ion charge. Also, hydrogen ions were neutralized and chlorine ions were
"forced" out of the region (significantly depleted). The cells in
this region being bathed in a high PH and high positive metal ion
concentration, are moved into another internal (cytoplasm) dynamic equilibrium
positive metal ion concentration state in which the various positive metal ion
concentrations are greatly increased and their concentration ratios
significantly changed. These metal ion complexes interact with both DNA binding
proteins and with specific ion complexes on specific DNA base pair sequences to
either form and or undo Z-DNA short segments at the beginning of some gene
sets. For the DNA reader enzymes to express the information in a gene sequence
set it has to mount onto a specific promoter protein which is wrapped onto a
specific sequence of B-DNA at the beginning of a gene sequence set. The
promoter protein in turn needs the blocker protein which commonly share their
binding DNA sequence site removed from the site, so as to allow the promoter
protein to move to the proper exact DNA base pair sequence for the DNA reader
enzyme mounting of the promoter protein and DNA transcription to begin. The
blocker proteins are usually removed by other proteins sent from other gene
sequences being read in the cell nucleus. If the promoter protein is being
blocked by its needed specific base pair sequence being in the Z-DNA
configuration, then this Z-DNA must be converted to the B-DNA configuration for
the gene set transcription to begin.
So, we
have a situation in which it is empirically known that positive metal ion
concentrations in the cell nucleus can drastically alter the access and
expression of gene sequence sets. Now how do these positive metal ion
complexes, which interact / complex with: 1) DNA directly, 2) with negative ion
complexes complexed with DNA, and 3) DNA’s complexed proteins, interact to open
up specific gene sequence sets? Consider a Z-DNA sequence blocking the binding
site of a promoter protein and therefore blocking DNA reader enzyme
transcription activity. By significantly changing the ionic environment at the
Z-DNA site, the Z-DNA can be converted to the B-DNA form and the promoter
protein can move into the site and bind with it and then the reader enzyme can
start transcription. One simple way to modify the ionic environment is to apply
a significant oscillating electric field at the Z-DNA location. This is easily
done by exposing the electrically conductive B-DNA segment, in which the Z-DNA
is at one or both of the antenna end points of, to one of the antennas’
resonant frequencies. The oscillating voltage induced in the antenna will be at
a maximum at the antenna ends, the Z-DNA location. Once the oscillating
voltage/electric field strength at the antenna end goes over some minimum value
it will be the dominate field determining ion concentrations in the region and
whether or not ion complexes will complex with the Z-DNA. Specifically, an
oscillating electric field suppresses complexing of ion complexes with DNA and
therefore suppresses Z-DNA formation and opens up Z-DNA blocked gene sequence
sets for transcription. Care must be taken not to build to strong of a resonant
voltage/electric field on the antenna end region to avoid DNA damage. Similar
oscillating voltage/electric field interactions between ion complexes, DNA
sequences, and blocker proteins can be invoked to remove some blocker proteins
and therefore start gene sequence transcription.
CONCLUSION:
By the judicious use of various frequencies of electromagnetic energy we can
destroy unwanted microbes, override genetic defects, control genetic expression
in such a way as to effectively halt and reverse aging, and repair and
regenerate the body totally, even form amputations and serve brain and spinal
injuries. We are potentially at the start of a brave new world for medicine,
biophysics, and biology (energy medicine, very few drugs required). Let us not
let this technology be developed only by the military and the medical elite.
Always remember: 1) The AMA is a monopolistic trade association interested in
controlling/owning your illness care rights and your illness care money, 2) The
pharmaceutical companies are not our friends and DO NOT HAVE OUR BEST INTERESTS
AT HEART. THEIR GOD IS MONEY. AS LONG AS THEY CAN GET YOU TO TAKE THE SYMPTOM
SUPPRESSING DRUG AND NOT TAKE CARE OF THE FUNDAMENTAL CAUSE OF YOUR PROBLEM,
YOU WILL NEED TO KEEP GOING TO THEIR LICENSED DRUG DEALER (YOUR ALOPATHIC
DOCTOR) AND SPEND YOUR MONEY. YOU ARE THEIR CASH COW. CAN YOU SAY MOO?
IF YOU FOUND THIS ARTICLE OF REAL VALUE, PLEASE MAKE A HARD COPY WHILE STILL AVAILABLE.
References:
1) Variable Range Hopping and
Electrical Conductivity along the DNA Double Helix by Z. G. Yu and Xueyu Song,
Physical Review Letters, 25, June 2001 Volume
86, Number 26.
2) Charge Transport along the Lambda DNA
Double Helix, P. Tran, B. Alavi, and G. Grunen, Physical Review Letters, Volume
85, Number 7, Page 1564-1567.
3) DNA and Conducing Electrons, H. W. Fink,
Visions and Reflections, Cell, Mol., Life Sci (CMLS), Volume 58, 2001, Page
1-3.
4) The Body Electric (Electromagnetism and
the Foundation of Life), by Robert O. Becker, M.D., and Gary Selden, ISBN
0-688-06971-1.
5) A Physicist’s View of the Use of Feeble
Electric Direct Currents To Repair Tissue and Replace Body Parts (Part One), by
Gary Wade, Health Freedom News (The magazine of The National Health Federation,
Monrovia, CA), February 1996, Page 22 – 33.
