Home | Contact Us | FAQ | Search & Site Map | Link to Us
Sign In | Join | Other 45 Sites in Network
Home
Discussion Groups
Biology
BiologyBotanyMicrobiologyEntomologyEvolutionPaleontology
Chemistry
General ChemistryAnalytical ChemistryElectrochemistryOrganic Synthesis
Earth Science
GeologyMineralogyOceanographyMeteorologyEarthquakes
Physics
General PhysicsResearchRelativityParticle PhysicsElectromagnetismFusionOpticsAcousticsNew Theories

Natural Science Forum / Biology / Biology / August 2008



Tip: Looking for answers? Try searching our database.

#71 beginning to explain why there is beta-amyloid and tau-protein in Alzheimer's ; new book: Metal Causation coupled with Weak-Protein-Point ^Theory of Medicine: Autism, Schizophrenia, Parkinson's, Prion, Alzheimer's

Thread view: 
Enable EMail Alerts  Start New Thread
Thread rating: 
Archimedes Plutonium - 13 Aug 2008 19:36 GMT
First I used the keywords of sulfur beta amyloid tau sulfur Alzheimer
and then I changed the word sulfur to that of "sulphur"

If MERCURY is the solo cause of these 5 diseases, it should explain
why there are two proteins involved in Alzheimers. The explanation,
I feel is probably due to the idea that mercury loves sulfur and
deforms molecules in the brain that have sulfur atoms.

Previously, I thought the pathology involved mercury deforming other
metal ions due to a "amalgam force". I abandon that mechanism, realizing
that the ability of mercury to scavenge sulfur atoms and deform
molecules containing sulfur is the primary mechanism.

So why is there two proteins gone awry in Alzheimer's. I focus on the
last listed hit below:

--- quoting several hits from Google ---

Specific saccharide compositions and methods for treating ...
424/709 , Sulfate 424/78.35 , Nitrogen or sulfur containing monomer
514/23 ... "Amyloid Plaque Core Protein in Alzheimer Disease and Down
Syndrome," Proc. ...
www.patentstorm.us/patents/6037327.html - Similar pages - Note this
by G Castillo - 2000 - Cited by 3 - Related articles - All 7 versions

Methods for using specific saccharides for treating alzheimer's ...
“Amyloid Plaque Core Protein in Alzheimer Disease and Down Syndrome,”
Proc. Natl. Acad. Sci. ... saccharide radical containing)
DOAI536/118Sulfur containing ...
www.patentstorm.us/patents/6767898.html - Similar pages - Note this
by AD Snow - 2004 - Related articles - All 4 versions
More results from www.patentstorm.us »

Medical Hypotheses : Oxidant free radical initiated chain ...
Selenium, sulfur amino acids and vitamin C provide reducing conditions.
... Specifically, Alzheimer's disease is characterized by tau protein
tangles in the ...
linkinghub.elsevier.com/retrieve/pii/S0306987704001100 - Similar pages -
Note this
by A Tappel - 2004 - Cited by 2 - Related articles - All 3 versions

Why is the amyloid beta peptide of Alzheimer’s disease neurotoxic?
to Ab. We showed computationally that the resulting sulfur radical .....
31 R. Bhatia, H. Lin and R. Lal, Fresh and globular amyloid beta protein ...
www.rsc.org/ej/DT/2008/b718601k.pdf - Similar pages - Note this
by A Rauk - 2008 - Related articles - All 2 versions

Molecular Psychiatry - Validation of amyloid-[beta] peptides in ...
by metal ions at met-35 produces a sulfuramyl free radical on the sulfur
atom.43 .... Tau protein, beta-amyloid (1-42) and S100B protein in
cerebrospinal ...
www.nature.com/mp/journal/v12/n7/full/4001967a.html - Similar pages -
Note this
by M Bibl - 2007 - Cited by 6 - Related articles - All 4 versions

NOW REPLACING sulfur with sulphur

CSF amyloid-{beta}-peptides in Alzheimer's disease, dementia with ...
-helical structure alters the electronic environment around the sulphur
of ..... Tau protein, beta-amyloid (1-42) and S100B protein in
cerebrospinal fluid ...
brain.oxfordjournals.org/cgi/content/full/129/5/1177 - Similar pages -
Note this
by M Bibl - 2006 - Cited by 24 - Related articles - All 5 versions

(WO/2007/145589) PEPTIDES THAT ARE CAPABLE OF BINDING TO AMYLOID ...
Hoshi, M., et al., Spherical aggregates of beta-amyloid (amylospheroid)
show high neurotoxicity and activate tau protein kinase I/glycogen
synthase ...
www.wipo.int/pctdb/en/wo.jsp?IA=WO2007145589&WO=2007145589&DISPLAY=DESC
- 39k - Cached - Similar pages - Note this

Elevated glutathione as a therapeutic strategy in Alzheimer's disease
Olney JW, Ho O, Rhee V. 1971. cytotoxic effect of acid and sulphur ...
regulates beta-amyloid precursor protein gene transcription in ...
doi.wiley.com/10.1002/ddr.10095 - Similar pages - Note this
by DA Butterfield - 2002 - Cited by 23 - Related articles - All 2 versions

1-[Alkyl], 1-[(heteroaryl)alkyl] and 1-[(aryl)alkyl]-7-pyridin-4 ...
It was later recognized that GSK3 beta was identical to tau protein
kinase 1 (TPK1), ... when Y represents an oxygen atom, a sulphur atom, a
sulfonyl group, ...
www.freepatentsonline.com/EP1184385.html - Similar pages - Note this

--- end quoting several hits from Google ---

Apparently the reason Alzheimer's involves two proteins of beta amyloid
and tau protein is that both involve sulfur (or to the British,
sulphur). Mercury reacts the same with molecules that contain sulfur.

In a sense, the fact that both tau-protein and beta-amyloid are involved
in Alzheimer's is a *Proof* that mercury is the underlying cause of
Alzheimer's.

In the other 5 diseases we have multiple proteins involved. In
Parkinson's we have a plethora of proteins other than alpha synuclein.
In Prion, we have a plethora of deformations of prion-protein, simply
called variants.

Why multiple proteins? Because they all have the same thing in common,
multiple sites of sulfur atoms in the molecules that mercury attacks.

Archimedes Plutonium
www.iw.net/~a_plutonium
whole entire Universe is just one big atom
where dots of the electron-dot-cloud are galaxies
plutonium.archimedes@gmail.com - 13 Aug 2008 20:04 GMT
(snipped)

> If MERCURY is the solo cause of these 5 diseases, it should explain
> why there are two proteins involved in Alzheimers. The explanation,
[quoted text clipped - 5 lines]
> that the ability of mercury to scavenge sulfur atoms and deform
> molecules containing sulfur is the primary mechanism.

I have two pictures of how mercury atoms cause these 5 diseases.

First, I can picture where the mercury-compound (ethyl-mercury or
methyl-mercury or some
other compound of mercury) is like a catalyst that comes in contact
with molecules in the brain
and deforms the molecule especially at sites of sulfur atoms. So in
this picture, I can see
mercury as a catalyst that remains unchanged itself but causing
deformations in the molecules
it contacts.

Second, I can picture mercury as becoming bound with molecules in the
brain and deforming them
such as a mutation in the synthesis of proteins and thus generating
the disease.

In Prion disease, I envision the pathology as where mercury acts like
a catalyst. Also in Alzheimers
where mercury as a catalyst can pretty well explain why it takes 10 or
more years for the disease
to unfold as it slowly deforms more and more proteins in the path of
the mercury catalyst.

In Autism, the actions of mercury seem to be of a bound-mercury at a
development site where nerves
are formed. Unlike a wandering catalyst of mercury that deforms
contacted proteins, in Autism the mercury
seems to stay put at a synthesis sequencing site and halts the
formation of nerves.

Now whether the male and female hormones plays a huge role in whether
Autism occurrs is a matter
to be researched. I think it plays a major role in why 75% of Autism
is boys. The female hormone
must be capable of removal of mercury excess much easier than the male
hormones of an early age.

In Parkinson's, apparently the mercury must be like Autism where it
latches to a site of the brain and
causes a deformation in the Synthesis Sequencing.

Archimedes Plutonium
www.iw.net/~a_plutonium
whole entire Universe is just one big atom
where dots of the electron-dot-cloud are galaxies
plutonium.archimedes@gmail.com - 13 Aug 2008 21:52 GMT
plutonium.archime...@gmail.com wrote:
> (snipped)
> >
> > If MERCURY is the solo cause of these 5 diseases, it should explain
> > why there are two proteins involved in Alzheimers. The explanation,
> > I feel is probably due to the idea that mercury loves sulfur and
> > deforms molecules in the brain that have sulfur atoms.

I should start some form of NOTEBOOK of notes on sulfur and mercury
inside of
cells. So let me start this notebook:

(1) I probably cannot get away with this statement "all proteins have
at least a sulfur
atom attached" I probably am correct when saying that 99% of protein
molecules
have a sulfur atom attached

(2) The sulfur atom attached to a protein has hydrogen atoms attached
to the sulfur
but when mercury atoms come in contact, the hydrogen is emitted

(3) When mercury binds with the sulfur atom on a protein, it can bind
with several
protein sulfur atoms depending if the mercury is divalent.

(4) Mercury will always deform the shape and thus the function of the
protein once
it binds and once the mercury leaves the protein.

(5) Mercury can act as a catalyst amoung protein molecules.

(6) Proteins are made from first a Messenger RNA.

(7) Messenger RNA goes to the cytoplasm of the cell to begin to make
proteins

(8) In the cytoplasm is Ribosomal RNA

(9) the Messenger RNA links with the Ribosomal RNA reading the message
and producing
the new protein

(10) sulfur atoms exist in all the Messenger RNA and the Ribosomal RNA

(11) thus, if mercury comes in contact with Messenger RNA or Ribosomal
RNA
could instantly cause the creation of rogue proteins

(12) Cells of the human body are actually two cells in one, where
mitochrondria-- the source
of energy of cells are actually independent bodies. So that
Mitochondria, in a sense, are smaller
cells inside of larger cells.

(13) the number of mitochrondria in muscle cells can number in the
thousands. I need to find
out a typical upper bound of mitochrondria

(14) Every mitochrondria has sulfur atoms

(15) None of the proteins associated with the 5 diseases is a protein
of the mitochrondria

(16) All the proteins associated with the 5 diseases are proteins of
the regular cell and were
created in the cytoplasm of the regular-cell

Comments:
From those notes, I can begin to visualize where mercury acts as a
catalyst and runs around creating
deformed proteins such as in Prion or Alzheimer's disease or in
Parkinson's disease. Also, the above
gives me a window into how mercury in a infant can get into the
cytoplasm of an infants brain and reside
and lodge in the Messenger RNA and Ribosomal RNA and cause for there
to be the lack of formation
of nerve-endings and thus create Autism.

Not sure yet why boys have 75% of Autism with girls 25%. Perhaps the
sex hormone causes girls to excrete
the mercury rather than lodge in the RNA.

Archimedes Plutonium
www.iw.net/~a_plutonium
whole entire Universe is just one big atom
where dots of the electron-dot-cloud are galaxies
 
Sign In
Join
My Latest Posts
My Monitored Threads
My Blog
My Photo Gallery
My Profile
My Homepage

Start New Thread
Enable EMail Alerts
Rate this Thread



©2009 Advenet LLC   Privacy Policy - Terms of Use
This website includes both content owned or controlled by Advenet as well as content owned or controlled by third parties.