Copyright 1988 All Right Reserved

9 The Virus, the Cell and fluids general information

12-35 The Cell, the operational site of the Virus

12 polymers making up the cell

17 proteins, enzymes, portals

27 character of the GENE polymer

18 instruction points on the gene

33 the Tag the individual identity

22 the NUB area making immunity

32 single cell life forms

35 polycellular life forms

36-64 The Polymers

38 formation

40 side groups

44 Phosphorus containing polymers

44 self duplication of polymers

47 Terminal groups importance

49 Clef polymers and the Cell wall

51 disturbing the cell wall

51-52 entry of the virus

51-54 Cell wall blocking the Virus

54-59 The Virus Polymer Structure-

54-58 a Gene Polymer fragment

58 Virus and Immunity

59 Preparation of a Virus –

64-73 Basis of Making ANTI-VIRUS CHEMICAL POLYMERS-

71 The ANTI-VIRUS Polymer

Laboratory preparation of ANTI-Virus Polymer

83-93 Testing ANTI - AIDS polymer

Extended preparation and testing anti-Virus Materials

95-99 Comments on the development of anti virus materials

THE VIRUS POLYMER

The virus is a polymer. A polymer is a connected group of chemical substances, joined together, in form like a "string" having a definite composition and functional capability with other polymers and chemicals.

The bodies organs and structures of animals and plants are largely made up of cells.

The actions carried out by the virus polymer occur in cells and in fluids in contact with cells.

The cells of a normal plant or animal are also largely composed of polymers.

The virus has the undesirable function of causing variation in the normal plant or animal cell from the normal function of the cell. (It is thus a Pathogen).

The synthesis or preparation of materials to apply to a plant or animal for the purpose of stopping the action of the virus, without altering the normal function of the cell, are dependent on a detailed understanding of the virus polymer chemistry and then the synthesis of new polymers to stop the action of the virus polymer.

Information on the cell chemistry and cell polymer function and also information on the virus polymer chemistry have now made the direct synthesis of anti-virus chemicals and polymers which do not interfere with the workings of cells a reality.

The formation and synthesis of new chemicals and polymers having a direct break-up action on the virus has been made and tested. The new chemicals and polymers restrict the activity of specific viruses such as those of AIDS and Herpes. So that chemicals and polymers, having the ability to stop the action of the AIDS and Herpes viruses, are available which protect the normal body and body parts from virus diseases, and allow normal healing and body processes to take place and recovery to occur.

The important Polymers in connection with the AIDS Virus and the conditions within which the AIDS virus functions are:

1. The AIDS virus itself- a polymer made up of phosphorus sugar and ammonia bases. It carries a program to effect the gene polymer within the cell. The AIDS virus multiplies itself by causing the gene polymer to make virus polymer from its own material.

2. The GENE polymer which is also a phosphorus sugar ammonia base polymer exists within the body cells. The GENE polymer (also called DNA) is the polymer responsible for programming the growth, the character, the immunity and digestion of the human person. When the GENE polymer is attacked by the VIRUS polymer, the GENE polymer alters its regular action and the GENE polymer alters its regular action of programming the actions and characteristics of the individual and only produces the VIRUS polymer. This causes the GENE polymer to stop directing the life process.

3. The MESSENGER polymer which is another phosphorus sugar ammonia base polymer (also called RNA) exists within all body cells of a human person. The MESSENGER polymer follows the instructions of the GENE polymer and is the pattern for and engineers the making of PROTEIN polymers and enzymes and antibodies. The MESSENGER polymer can also be attacked by an AIDS VIRUS polymer and thereby re-programmed so that it makes the VIRUS polymer rather than proteins, antibodies and enzymes.

4. Body proteins are the polymers that form the structures within the cells. The cell protein polymers form (with cells) the muscles and organs of the body of human beings and animals.

The protein polymers are made in the cell at the direction of the MESSENGER polymers. They are made from "amino acids" of many varieties which get into the cell as the result of digestion of nutriments. There are many special proteins including antibodies, enzymes and pigments.

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The three polymer systems GENE polymer, MESSENGER polymer and PROTEIN are dependent on each other for their formation, and on them depends the life of the human, animal, or plant. The break up of one system of polymers by a VIRUS polymer results in the ending of the ability of a living thing to function.

THE VIRUS- a reactive polymer chain functioning within the inclosure of a biological cell and the liquid surrounding the cell. The virus interferes with the normal organization of the cell.

THE BIOLOGICAL CELL- is an inclosed process domain, holding a unit organization derived from organizing and high molecular weight polymers. (Generally phosphoric acid polymers with saccharide and cycloamine groups- genetic material and also polyamid polymers with reactive organic side groups- protein material). The unit organization has the capability of maintaining its identity and of duplicating itself.

The cell (the inclosed space and its contents) requires a bounded domain to carry forward without interruption the organizational requirements of raw material supply, systematic production, and the retention of its identity.

Each of the many types of Biological cell conforms to these basics of organization.

The cell thus functions from "large"- high molecular weight chemical polymers (in the mol weight range of 1000 to 25000 or higher) operating in the presence of "small" chemicals- low molecular weight chemicals, up to 1000.

The cell is part of an environment and the environment is part of the cell.

In environments conducive to biological operation, many small chemicals exist. Among the small chemicals are water, oxygen, carbon dioxide, nitrogen, ammonia-metal ions: sodium, potassium, magnesium, zinc, calcium, manganese, cobalt, iron, molybdenum-

anions: chlorides, iodides, phosphates, sulphates, nitrates-

organics : dibasic acids, alcohols, ketones, saccharides, mondasic acids, aromatics-

nitrogen organics: diamines, cyclic nitrogen organics,

nitrogenous ketones, amino acids-

mineral fragments: asbestos, limestone, silicates, phosphates,

sulphides, oxides.

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THE NATURE AND LOCATION OF THE VIRUS-

--- The biological cell an operational center for the virus ---

Important parts of the functioning of the "biological cell" are dependent on the use, transmission, and control of "chain" structures.

The chain structures are put together from small chemical units which are repeatedly attached one unit to a previous unit. Thus when a chain of amino acids is made, a protein results; when a chain of saccharide materials is made, a cellulose fiber results;

When a chain of phosphate radicals which carry saccharides to which cyclic organic amines are attached, then a Phosphogenetic chain results.

The chemical units (monomers), which make up the chain (polymer) generally use the same chemistry to attach one unit to another in a "straight" sequence, but the constituents of the monomers other than the attaching groups are not necessarily identical. Each monomer in the chain may carry available reactive groups,

available, but not involved in chain formation. Thus many chains in biological cells are reactable entities dependent on the chemical nature of the side group, the number on the chain and the length of the chain. The chains, dependent on function, may be from 500 monomer units long to 5000 monomer units long.

The genetic process is really a means of achieving biological products of high chain length, of specific properties and using the individual characteristics and products of each for construction, synthesis, digestion and control.

RELATED CHAIN ENTITIES-- The protein chain is a chain of amino acids.

The enzyme is a chain of amino acids terminated in a functioning metal.

The genetic chain is a chain of phosphate groups which carry functional side groups of saccharide attached to cyclic amine groups.

An Enzyme is a protein chain with a metal termination. The protein is a chain of amino acids. The metal terminal is required for the enzyme to function. The Enzyme causes organic reactions to occur.

A GENETIC chain is a chain of phosphorus oxide groups to which sugar moles are attached along the chain and cyclic amine groups are attached to the sugar groups. The numerous Phosphogenetic

chains in a cell depend on one "starting" type of Phosphogenetic chain, which has the functions of "pointing" the assembly of Phosphogenetic chains derived from the starting "pointer Phosphogenetic chain".

There are many "Pointer Phosphogenetic Chains", each one covering a Product Domain. Each Pointer Phosphogenetic Chain is capable of

1. Reproducing itself as the prime genetic material for transfer to another cell-
2. Producing a Messenger Phosphogenetic Chain. The messenger chain carries the pattern and template for the production of a "product output". The Messenger Chain actively engages the "product" formation. The Messenger chain cannot reproduce itself. The Genetic chain requires a metal terminating group like the Enzyme does. The Messenger genetic chain, derived from the Pointer chain, which is in the Chromosome, accepts and reacts with amino acids, one by one, attaching the amino acids together thereby forming a long chain of amino acids. The long chain of amino acids are a protein and released when complete.

The Genetic chain is many hundreds of phosphate-sugar-cyclic amines in length. (It has to be to synthesize proteins many hundreds of amino acids in length).

When a Phosphogenetic-Genetic chain is fragmented, due to a cellular breakdown or mechanical disruption, fragments of the Messenger genetic chain float free. These, with other cellular contents, move into any surrounding or flowing fluid. When these fragments become attached (by chance) to a suitable metal

terminating material, a shorter chain Genetic material with a new function is formed. This new Genetic material is called a VIRUS.

The virus is capable of attacking a normal functioning Messenger Genetic chain, after penetrating inside a cell, and instead of the chain making proteins the genetic chain makes reproductions of the Virus using the genetic material of the cellular genetic chain to reproduce itself. Thus Viruses increase by invading other cells and stopping the activity of the "host" cells and reproduces itself. Now two virus entities pass into the intracellular fluid and invade two cells. In each of these two cells the virus produces two viruses which pass into the intracellular fluid. Thus the number of Virus particles doubles very rapidly as the number of invaded cells increase.

From the standpoint of origin, the Virus, using a fragment of displaced genetic chain, exists only after cellular function and structure have been established. New viruses are in process of assembly at any time displaced fragments of cellular genetic material and suitable metallic terminators are available.

Normally the genetic chain synthesizes proteins from amino acids by starting at one end of the genetic chain and proceeding to add amino acids to each other along the genetic chain. As the protein is formed each addition is being directed by the corresponding nitrogen ring unit of the genetic chain. When complete the protein is released. If the protein has a metallic termination it is an enzyme: if it is not terminated it is a structural or fundamental protein.

The Virus attacks the genetic chain in the middle and causes the production of virus genetic material from using one portion of the chain of normal genetic sequence. Thus the new Virus consists of genetic materials (phosphorus-oxide-sugar-cyclic-nitrogen-carbon items) derived from a part of the normal genetic chain.

So one virus (the attack virus) produces another virus (the chip virus) and two viruses result from each attack. A metal terminal is absorbed outside the cell. The two viruses pass out of the cell. After leaving the cell, since they are identical, both are attack-viruses. The virus does not use the genetic material of which it is composed to produce protein.

However, as the attack virus is producing the chip virus, the normal genetic sequence is producing proteins from amino acids in the cell, as this protein in formation reaches the place where the virus is attached to the normal chain, the protein continues to form along the virus sequence until it reaches the end. This single protein is thus made up of two distinct sequences, one from part of the normal genetic pattern, one from the virus genetic pattern. This protein passes out of the cell after both viruses

leave the cell, and goes into the general circulatory medium. When this protein (which tends to orient on a cell wall due to the protein portion derived from the normal portion of its makeup) comes in position near an attack virus, this normal – plus-viral synthesized protein- using the viral derived portion of its configuration, attaches to the genetic functions of the attack virus and "fills in" the genetic function of the virus, and the remaining tail –originating from the normal genetic sequence, covers over the terminal function of the virus and interferes with the virus functioning. Such a protein is called INTERFERON.

The Interferon therefore blocks the activity of the virus when both interferon and virus are in motion within the extracellular fluid. Dilution of both the interferon and the virus by considerable amounts of extracellular fluid, favors the continued existence of the virus, because the probability of Interferon meeting and attaching to virus decreases as dilution of both increase. Meanwhile, the virus is presented with many cells which it can invade and use as a base for further production of itself.

In many cases the interferon completely blocks the activity and therefore the survival of the Virus, but not in all cases.

Within the extracellular fluid, through which the virus must pass, there are other cellular breakdown fragments. These may be of a type which could add on to the virus, thus altering its invading and reproductive capability.

The virus is limited to the type of cell it can attack. Viruses originate from and propagate only from cells containing the Phosphogenetic-saccharide-cyclic-nitrogen production or reproduction system. Thus the virus does not have a reproductive capacity with erythrocytes.

Due to its origin, the virus is approximately specific to the cell genetic class of its origin and therefore to those cellular structures carrying commonly compatible genetic entities.

Viruses propagate only from cellular material of actively Producing cells, not actively Reproducing cells. The virus is transmitted in intracellular fluid within an organism and between organisms.

The virus originates from and attacks only the Phosphogenetic operation of those cells in rapid production of chemical protein materials which action is present in considerable concentrations of, for instance B. Coli and the rapidly producing progenitors of white blood cells (both leucocytes and monocytes). The white blood cells are carriers of components responsible for "immunity" to bacterial infection. Damage to these progenitors of immunity bearing cells, results in an immunity which is damaged. That is, an immunity deficiency which is acquired by damage to the immunity cell progenitors. During an infection by bacteria, the demand for white cells is high, causing a demand for immune carrying cells. If the producers of the immune cells are damaged, white cells are not produced, immunity centers do not function and infection proceeds unchecked. This is the sequence of "acquired immunity deficiency".

Viruses do not arise during embryonic growth, because free displaced fragmented material does not flow to external locations.

THE CELL

The concept of a Biological Cell reduced to essential terms is – an instruction dependent agency, dependent on transmitted instructions.

The Virus is an instruction in part similar to a set of instructions within a Cell and in part instructions different from the functional instructions of the cell.

Other effects that change the instructions within a cell are- physical damage to the instruction and chemical damage to the instructions.

Quite different is the damage to the instruction mechanics of the cell by the entrance of a small bacterial product chemical. The immunity process provides a means for the instruction assembly to check the on the structural variation of a foreign structure, and thereafter act accordingly.

THE CELL from the operational standpoint is an assembly of interconnected regions. The regions are permeable to each other under conditions determined by each region and by the full assembly of regions.

The cell assembly is arranged to provide for its own reproduction (or to be part of a cell group arranging for reproduction of the group).

The plan of process, reactions and reproduction are within the program (genetic) region of the cell, but the triggers (or events) which activate the continuity processes come from outside the cell and are the result of environment materials and physical conditions, which are in fact the "trigger" items elucidating responses within the cell.

The overall container identifying the individual cell and enabling many reactions to take place in sequence is the "Cell Wall".

THE VIRUS- a reactive polymer chain functioning within the inclosure of a biological cell and the liquid surrounding the cell. The Virus interferes with the normal organization of the cell.

THE BIOLOGICAL CELL- is an inclosed process domain, holding a unit organization derived from organizing polymers. – Generally phosphoric acid polymers with saccharide and cycloamine groups- genetic material and also polyamid polymers with reactive organic side groups- protein material. The unit organization has the capability of maintaining its identity and of duplicating itself.

The cell (the inclosed space and its contents) requires a bounded domain to carry forward without interruption the organizational requirements of raw material supply, systematic production, and the retention of its identity.

Each of the many types of Biological cell conforms to these basics of organization.

The cell thus functions from "large" – high molecular weight chemical polymers (in the mol weight range of 100 to 25000 or higher) in the presence of "small" chemicals – low molecular weight chemicals, up to 1000.

The cell is part of an environment and the environment is part of the cell.

In environments conducive to biological operation, many small chemicals exist. Among the small chemicals are

water, oxygen, carbon dioxide, nitrogen, ammonia-

metal ions: sodium, potassium, magnesium, zinc, calcium, manganese, cobalt, iron, molybdenum-

anions: chlorides, iodides, phosphates, sulphates, nitrates-

organics : dibasic acids, alcohols, ketones, saccharides, mondasic

acids, aromatics-

nitrogen organics: diamines, cyclic nitrogen organics,

nitrogenous ketones, amino acids-

mineral fragments: asbestos, limestone, silicates, phosphates,

sulphides, oxides.

THE POINTER (DNA)

Consists of a chain of phosphoric acid monomers to each monomer unit is attached a deoxyribose (pentose sugar unit) to which is attached one of four possible cyclic amine units, the sequence of the units makes up a code and impressing a version of the code on the offspring and for forming the offspring of the pointer chain. It does not of itself carry identity groups.

It can duplicate itself.

IT can be transferred between many types of life.

It cannot penetrate cells.

The polyphosphoric acid chain is terminated. The termination determines the output function of the chain.

It can append portions of other pointers.

The Pointer parts are altered by chemicals which do penetrate the cell.

It can be active or inactive for long periods.

It reproduces itself for age renewal.

It can produce Messenger chains.

THE MESSENGER CHAIN (RNA)

Is a phosphoric acid polymer chain containing on each polymer unit a RIBOSE (pentosan sugar) –not deoxygenated as in the pointer but attached to each pentosan group is one of four possible cyclo amine groups.

The Messenger chain carries a program sequence of cyclic amines in an arrangement placed in the chain by the Pointer from which it was derived.

It can produce a protein also according to the pattern derived from the parent Pointer.

It can move around cellular compartments.

It is activated by specific terminals.

It is altered by chemicals and by being broken up by activated particles of similar Messenger chains.

The Messenger Produces protein chains (Polyamid chains).

The POLYAMID (PROTEIN CHAINS)

It is fundamentally a polyamine chain with side groups as determined by the plan (of sidegroups) of the predecessor messenger chain. The chain may contain "recognition areas" enabling the protein to identify proteins not derived from Pointers and Messengers of similar species origin.

It can convert to a structure. It can convert (by suitable termination) into an antibody. It can convert to a digestive enzyme. It can convert to a protein which breaks other specific proteins into smaller (useful and reactive) fragments.

It can convert to enzymes for digestion of non-protein fragments- cellulose, pentoses, dibasic acids, lipids, terpenes.

It can convert to chains sequestering inorganic ions.

It can convert to secondary controllers.

The Rack of Pointers is an assembly of Pointers –within a cell- making a variety of outputs available from a consolidated center. The Rack overcomes the limitation of the single Pointer, since one Pointer produces one Messenger, produces (multiples) of one protein which protein has one capability.

The group action results in a group of special functions, the interaction of which makes new results possible.

The Rack of Pointers sets up its own compartment.

The rack of Pointers reproduces (when each single Pointer reproduces) as a unit.

In the rack each or any Pointer may be active at any time.

The Pointer group, by division of output and cooperative timing, manages the Cell according to methods and responses set out within the pointers and therefore the Pointer Assembly Program.

In single cell bioforms the Pointer Groups may all be functional as their part in regulating the entire Cell by input to Cell responses within the Cell.

Cell specialization (as evident in Polycellular Bioforms) originates from selection of the activation of a few of the activities of each Pointer rack in each associated cell.

THE ORIGIN (and predecessors) of the Pointer and Pointer Groups occurs when PORTAL BUNDLES produce rudimentary Pointer and Messenger units. Such units when enhanced and added to by use and adaptation, become presently recognizable Pointer and Messenger groups.

THE COMMON FEATURES OF CELLS-

The CELL WALL establishes a distinct unit identity. It provides a protective envelope.

Structure provides framework for the functions.

Circulatory avenues through the structure and functioning components- connecting, isolating, and conveying.

Spaces for containing the output of functioning components.

A RACK of Essential Polymer Pointer Chains (DNA) providing programs for structure, growth, maintenance and reproduction. Programs carried out by the Messenger Polymers (DNA).

A NUB area, to synthesize Pointer Chains (DNA) from small chunks of Pointer Chains providing adaptation from external stimuli to produce protective program information, for use by Messenger chains to synthesize antibodies.

A Messenger Chain area, where Messenger Chains, executing Pointer Chain programs, provide by synthesis polymer materials for

structure, protection, metabolism, motion.

Cells are dependent on aqueous media.

A Portal Chain area. Portals provide chemicals useful to the Messenger Chains by synthesis from simple compounds (from external sources).

In biological systems either monocellular or polycellular, the central integrity of the cell becomes clear when it is seen that the cells of many animals and plants as well as unicellular life forms, grow and survive in culture under self guidance as if the cell were unicellular.

POINTER AND MESSENGER PHOSPHOGENETIC CHAINS-

Central to the "life" processes of many unicellular