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V.e.c.t.o.r. Experiments


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#1 VictorMedvil

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Posted 06 August 2019 - 07:53 AM

I will start by stating the meaning of the acronym V.E.C.T.O.R. being Viral Engineering Collaborative Transgenic Organism Research or V.E.C.T.O.R., I will be explaining the function and research of each sub project within this project at a later time, I don't have the time to outline the full details of the V.E.C.T.O.R. experiments right now but I will at a later time, but this is a project but it is a thread combining of all my personal research into Viral Engineering over the last 7 years, which I wish to put into a single place.

 

Retroviral-Engineering-SMAC-1.png


Edited by VictorMedvil, 06 August 2019 - 08:30 AM.


#2 VictorMedvil

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Posted 06 August 2019 - 08:30 AM

I will start with the first project within V.E.C.T.O.R.

 

Name: Precursor MV-3 

 

Type: Self Terminating Multi-Valent  Retroviral Vector for Lung Cancer Gene Therapy

 

Gene Map:

New-Bitmap-Image-2.png

 

Status: Never created, Model tested by protein folding Theoretically works.

 

Thoughts: This was my first experiment with Viral Vectors this was made for a biochemistry final project for my professor back in March 2013  this was before the first gene therapy trials for Retroviral Vectors in 2014 against leukemia(https://www.rt.com/n...tient-cure-940/), I had hopes that this could be used to insert a suicide gene into lung cells, blood vessel cells, and white blood cells that gained cancer and could recognize them with a CRISPR-like Synthetic Endonuclease the cancerous genes and delete them causing suicide of the cancerous tissue. This had a special trait which was the Self Terminating Endonuclease Loop which would cause the Retroviral Vector to stop production of the Caspid and DNA Machinery upon one loop making a single reproduction before production was canceled as I said this was before Addgene and Many companies that later popularized the other model without LTR5' and LTR3' around the entire virus, it was unknown how to exactly control the replication of the Virus into a Vector. This was also right as I started reading the book Principals of Retroviral Vector Design (https://www.ncbi.nlm...books/NBK19423/). I remember a professor calling them "Things" and I laughed because I understood that they are "Things" too, but little did either of us realize how important these "Things" would become back then not only to myself but this entire world they were just a subject that hadn't been researched very much in some dusty archive, but something changed after that, I called them "Viral Nanobots" after that.

 

Mid 2013 Video about programmable nanobots possible?

 

Mid 2013 The First mention of "Viral Nanobots" 

 

Late 2013, Gene Therapy using Retroviruses, this person had a amazing adaption which is commonly used in all vectors now. LTR3' and LTR5' outside the genome.


Edited by VictorMedvil, 06 August 2019 - 05:38 PM.


#3 VictorMedvil

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Posted 06 August 2019 - 05:58 PM

The Next Project within V.E.C.T.O.R. early 2014.

 

Name: Zombie Virus MV-5

 

Type: LEGENDARY Multi-valent Viral Genetic Warfare Agent

 

Gene Map:

Zu0ki00-gif-1e80778e557ec7199671e1870316

 

Status: Never Created, Model Tested by Protein Folding, Infectivity Simulation, and Viral Construction Theoretically Works but could have carrying capacity problems.

 

Thoughts: This was a Viral Genetic Warfare Agent constructed because I watched Resident Evil then I was convinced I could create a zombie virus from the movie. This was for Halloween on Facebook in 2014 for dramatic effect, it merited a FBI visit where the FBI asked about the creation of biochemical weapons the FBI thought that it would be a dangerous weapon if ever constructed and could have serious military applications. The design was somewhat successful until 2014 when I seriously questioned the carrying capacity of the nanobot which could cause issues with replication of the virus if ever deployed. The Inspiration for this nanobot was from Ebolapox that the Russian government had constructed Ebolapox I was determined I would create something worse(https://www.quora.co...preparat-a-hoax) that maybe the US government would find useful. A flash drive containing all research about Zombie Virus MV-5 and Precursor MV-3 was gifted to the FBI for their visit. The question you must now ask yourself is did the government create devices like this after this meeting that are classified?(https://www.national...-virus-science/)

 

 


Edited by VictorMedvil, 06 August 2019 - 06:49 PM.


#4 VictorMedvil

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Posted 07 August 2019 - 10:18 AM

Next Project in V.E.C.T.O.R. Mid 2014

 

Name: Genetic Warfare Agent MV-27

 

Type: Multi-Valent Viral Genetic Warfare Agent

 

Gene Map: 27 Species Chimera, Gene Permutation Structure(https://en.wikipedia...ion_in_proteins), Gene(1,1) ..... Gene (X,27)

 

Status: Never Created, Model Tested by Protein Folding,Infectivity Simulation, and Viral Construction, Has Carrying Capacity problems the genome is too long for any caspid to contain.

 

Thoughts: This was the most powerful genetic warfare agent ever considered it is a fusion of many virulent and extremely lethal pathogens all BSL-2 to BSL-4 including Smallpox, Rabies, S.A.R.S., and 24 others. This device is probably impossible to construct due to the extreme length which is around 270,000 bp, there is no capsid in nature that can contain a virus of that DNA/RNA length, if it ever were to be created to definately has the possibility of creating a global pandemic given the nature of the pathogens included which have air-borne, blood-borne and touch-borne traits, this was the masterpiece of my Chimera experiments within V.E.C.T.O.R. within the hostile genetic warfare agents with a simple genetic design all that is missing is a capsid that can actually carry that much DNA/RNA. This could be theoretically constructed using a synthetic caspid but I will not go into too much detail about how to construct the genetic warfare agents as they have intentional flaws as I never wanted them used.

 

 


Edited by VictorMedvil, 18 September 2019 - 10:55 AM.


#5 VictorMedvil

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Posted 07 August 2019 - 10:52 AM

Next Project within V.E.C.T.O.R, Mid 2014

 

Name: Pholus Mutagen MV-21

 

Type: Multi-Valent Plant Viral Genetic Warfare Agent

 

Gene Map: 21 Plant Viral Species Chimera, Gene Permutation Structure(https://en.wikipedia...ion_in_proteins), Gene(1,1) ..... Gene (X,21)

 

Status: Never Created, Model Tested by Protein Folding,Infectivity Simulation, and Viral Construction, Has Carrying Capacity problems the genome is too long for any caspid to contain.

 

Thoughts: The concept behind this device was to make one that would only effect plants this would spread the disease into plants causing worldwide famine and the death of 21 different species of crop bearing plants such as Corn,Rice,Soy Beans, Oranges, and 17 other species of plants that are commonly used as food crops. This device also has the problem of caspid size as no caspid can carry this like the MV-27 a synthetic caspid would need to be used if ever this were to be constructed given that it is around 210,000 bp in DNA/RNA length these are highly virulent to plants and only plants which would most likely ecocide the planet killing all crops of 21 different species. This Virus would create a worldwide famine as the MV-27 this has built in issues with carrying capacity these unable to be constructed on purpose as to not allow it to fall into the hands of those that would abuse this technology.

 


Edited by VictorMedvil, 07 August 2019 - 11:20 AM.


#6 VictorMedvil

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Posted 14 August 2019 - 01:28 AM

Continuing the Next Project within V.E.C.T.O.R. Late 2014.

 

Name: Ebola Vaccine/Vector

 

Type: Uni-valent Pseudo-typed Viral Vector Vaccine

 

Status: Never Created,Model tested by Protein Folding and Viral Structural Simulation, awaiting synthesis.

 

Gene Map

New-Bitmap-Image-2.png

 

Thoughts: This Vector/Vaccine is a standard retroviral vector pseudo-typed with ebola's glycoprotein to target the same cells that ebola targets in its infection, basically the same targetting system that the virus uses is used to target the infected cells. This Vector/Vaccine edits the cells making them immune making the virus unable to replicate within these cells that have been vaccinated to ebola virus this vector hunter-seeks and cleaves out the L,VP30,VP40, and VP24 protein constructs of ebola as a added gene to the human genome which its target is a RNA polymerase,RNA Transcription, and Viral Assembly which replicates the virus's DNA. Upon finding its L Target it will destroy the gene making ebola virus unable to replicate. Upon Finding the VP30 Target it will destroy the gene doing RNA Transcription, then upon find VP40 and VP 24 it will destroy the genes doing Viral Assembly deactivating the virus forever.  This is a type of genetic engineering that makes the cells immune to ebola by placing in a defense Gene/protein that hunter seeks and that kills ebola virus upon contact, if ebola virus begins to infect cells that have been made genetically immune to the virus, the virus will be deactivated on the genetic level by the vaccinated cells by this vector/vaccine. These genes L,VP30,VP40, and VP24 being silenced by destruction of the genetic code itself by the Cas9 + Guide RNA Pair. Personally, I have always wanted to test this vector/vaccine in the real world but have never had the opportunity to test it. This is the definition of a Viral Nanobot being used as a gene disruption device but in a helpful way against Ebola Virus.


Edited by VictorMedvil, 14 August 2019 - 02:07 AM.


#7 VictorMedvil

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Posted 16 August 2019 - 06:51 AM

Continuing with the Next Project within V.E.C.T.O.R., Early 2015

 

Name: Norovirus Vector/Vaccine

 

Type: Uni-valent Pseudo-typed Viral Vector Vaccine

 

Status:Never Created,Model tested by Protein Folding and Viral Structural Simulation, awaiting synthesis.

 

Gene Map

New-Bitmap-Image-2.png

Thoughts: This Norovirus uses Cas9 to silence genomic targets that replicate Norovirus such as Norovirus Pol and Norovirus Protease, once the set of Guide RNA is inserted into the cell then the cas9 gene will cleave on the target DNA causing a mutation of the target DNA. This cleaving of the DNA will damage the genes associated with Norovirus Pol and Norovirus Protease, This vaccine will insert Cas9 + Guide RNA Combo into the cellular DNA making the cell immune to Norovirus this stopping the replication of Norovirus making the virus unable to make copies of itself genetically by damaging the machinery. The cellular targetting of the vector is the same as Norovirus using the Glycoproteins for Norovirus itself to enter into the cell.


Edited by VictorMedvil, 16 August 2019 - 07:12 AM.


#8 VictorMedvil

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Posted 20 August 2019 - 09:49 PM

Continuing with the Next Project within V.E.C.T.O.R., Mid 2015

 

Name: Enterovirus D68 Vector/Vaccine 

 

Type: Uni-valent Pseudo-typed Viral Vector Vaccine

 

Status:Never Created,Model tested by Protein Folding and Viral Structural Simulation, awaiting synthesis.

 

Gene Map

New-Bitmap-Image-2.png

 

Thoughts: This Vector cleaves all of the genes besides the structural genes of EV D68 causing the virus to fail in replication much like the two previous viruses but this will add the Gene to every cell in the human body as the structure of EV D68 is not a glycoprotein and does not have a lipid envelope, thus the alterations must be done to all cells within the body to prevent infection by this virus the glycoproteins cannot just be cloned, but this still uses CRISPR inserted with the genome as a viral immunity protein that cleaves on genetic targets to interrupt reproduction of the virus. The gene VSV-G is used to target every cell in the human body in absence of a targetting protein for the virus that we are trying to make a vaccine against.


Edited by VictorMedvil, 20 August 2019 - 09:51 PM.


#9 VictorMedvil

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Posted 21 August 2019 - 07:39 AM

 Further, the Next Project within V.E.C.T.O.R., Late 2015

 

Name: MV-2 (Rabies/HIV) Vector

 

Type: Multi-valent Pseudo-typed Retroviral Vector

 

Status:Never Created,Model tested by Protein Folding and Viral Structural Simulation, awaiting synthesis method Oligonucleotide Synthesis.

 

Gene Map based on 2nd Generation Vector

Untitled.png

 

Gene Map based on 3rd Generation Vector

New-Bitmap-Image-2.png

 

Thoughts: The 2nd generation gene map was created using a program for from DNA base pairs to gene map, this is the Packaging Plasmid for the MV-2 , basically it is like the other MV-5 earlier discussed but the vector version if LTR3' and LTR5' were placed around any DNA then this vector would become active taking that DNA and not the entire vector producing plasmid, this is a 2nd generation Multi-valent Retroviral Vector versus the 3rd Generation Multi-valent Retroviral Vectors I have used in the past making the 2nd generation vector Ret and Tat dependent, There are two versions of this the 3rd and 2nd generation Retroviral Vector versions. Personally, I think the 2nd generation version has a sloppy code versus the 3rd generation but this targets T-cells and Nerve cells for specific and exacting targeting of cell types. This was going to be created for Addgene in 2018 but was never constructed due to legal issues that arose between me and Addgene about whom actually had control over the plasmid unless it was paid for, thus this was never created as a 4th generation Multi-valent Retroviral Vector for that company, which I was interested in selling it but I wanted paid something other than plasmids for it to be sold as they currently pay you for your work in plasmids only if you donate a plasmid. I was not interested in being paid in plasmids for my work and I we couldn't reach an agreement about it as I sought to pursue industrial production and not open sourced research, so it was never created by oligonucleotide synthesis, then me and that company parted ways when we told each other to never contact each other again then they destroyed the previous plasmids I had sent in, which retain as mine, but the original code for this was created long before 2018 in late 2015.


Edited by VictorMedvil, 21 August 2019 - 05:49 PM.


#10 VictorMedvil

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Posted 21 August 2019 - 08:36 PM

Further, the Next Project within V.E.C.T.O.R., Early 2016

 

Name: MRHHS MV-5  Vector

 

Type: Multi-valent Pseudo-typed Retroviral Vector

 

Status:Never Created,Model tested by Protein Folding and Viral Structural Simulation, awaiting synthesis method Oligonucleotide Synthesis.

 

Gene Map based on 2nd generation vector

 

Untitled.png

 

Gene Map based on 3rd Generation Vector

New-Bitmap-Image-2.png

 

Thoughts: This is another Multivalent Retroviral Vector that specifically targets certain tissue types while ignoring others these glycoproteins target Nerve,T-Cell,Liver,Lung,and Skin tissues in the body which is a more exacting way to target cell types to make alterations, this has a DNA insert between the LTR3' and LTR5' of Cas9 for CRISPR editing unlike the MV-2. This was another vector that was going to be produced in 2018 for Addgene had they accepted my terms but as of now because of the disagreement between me and Addgene it was never constructed physically. The Gene patterns and DNA code is much older than 2018 going back to 2016 while I was attempting to make Multivalent Retroviral Vectors that worked, the glycoproteins all connect upon a C-Terminal on the Envelope of the vector.


Edited by VictorMedvil, 21 August 2019 - 08:37 PM.


#11 VictorMedvil

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Posted 27 August 2019 - 12:19 PM

Further, the Next Project within V.E.C.T.O.R., mid 2016

 

Name:  Chimeric Bacteriophage MV-3

 

Type: Multi-valent Chimeric Bacteriophage

 

Status:Created,Model tested by Protein Folding and Viral Structural Simulation, Method of Synthesis DNA recombination. 

 

Gene Map

New-Bitmap-Image-2.png

 

Culture Picture

WIN-20190827-13-55-21-Pro.jpg

 

Thoughts: This was a experiment into antibacterial chimera viruses that would kill antibiotic resistant bacteria these are a genetic recombination strain of chimeric bacteriophages being a chimera of Φx174,T2, and T4 which are kept in cold storage below 50 F this being the perfect temperature for bacteriophage storage. This is actually is a Non synthetic MV-3 made from the living viruses and not constructed DNA, they are absolutely harmless to animals and plants but deadly to bacteria of all kinds almost being as lethal to bacteria as anti-bacterial sprays which kill 99.9% of all types of bacteria, this having almost the same effect but this is a persistent agent meaning like antibiotics, bacteriophages will continue to kill bacteria but unlike antibiotics they cannot have a resistance gained against these virii meaning they will still kill antibiotic resistant bacteria 99.9% of the time. This was overall successful Chimeric Bacteriophage MV-3 which physically function, they are produced using Synthetic machine bacteria(Metamorphic Gel 45) which replicate, the bacteriophage structure allows for a much larger genetic cargo having almost 20x the size of genetic data as standard retroviral vectors which have been already created in the lab, so there was no point of created them again. This Chimeric bacteriophage uses the lytic cycle and not lysogenic cycle kills the cellular host after infection releasing more of the Chimeric bacteriophages upon killing bacteria, the actual color of this is bright orange in the bright light or Dark Orange in less light  which is another way you can tell it is a successful chimera as Φx174 are naturally Red, T2 naturally black and T4 naturally Yellow. This is the only 500 ml of this chimera known to exist which does not exist in nature, which is contained in a 500 ml borosilcate flask air tight sealed, the yellow at the bottom of this picture is actually agar feeding solution for the machine bacteria(Metamorphic Gel 45) to eat that produce the chimeric bacteriophage, this is a 3 year old culture of them in the present picture.

 

 

Even Bacteriophages can benefit from genetic engineering.


Edited by VictorMedvil, 27 August 2019 - 01:05 PM.


#12 VictorMedvil

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Posted 27 August 2019 - 01:49 PM

Further, the Next Project within V.E.C.T.O.R., Late 2016

 

Name:  Extremophillic Chimeric Chickenpox MV-3

 

Type: Multi-valent Controlled Evolved Extremophile Chimeric Virus

 

Status:Created,Model tested by Protein Folding and Viral Structural Simulation, Method of Synthesis DNA recombination and Directed Evolution.

 

Gene Map 

New-Bitmap-Image-2.png

 

 

Culture Picture

WIN-20190827-15-35-28-Pro.jpg

 

Thoughts: This was an experiment in controlled evolution which basically means dramatically changing the environment on samples then recombining the surviving organisms to this MV-3, the change making mutated versions of the organisms in this case chickenpox. First the chickenpox virus was exposed to Cold Temperatures for a long period of time, then High Temperatures for a long period of time making a extremophile strain with a caspid that could survive these conditions, Then another sample of the same virus was exposed to extremely high temperatures, while another sample was exposed to extremely low temperatures below freezing, then the surviving samples of each of the three's genomes were recombined from the mutated variants to survive Mid range Cold/Hot, Extreme Cold, and Extreme Heat making this Extremophillic Chickenpox MV-3 strain being taken from 3 differently evolved by conditions versions of the same virus. The caspid of this virus can survive in almost any conditions of temperature based on the  directed evolution of the gene making a synthetic gene which was the purpose of this experiment to make that synthetic Caspid Gene. The color of this MV-3 being Bright Yellow in and out of light which is the natural color of chickenpox virus cultures, this virus not being particularly dangerous as I have had chickenpox along with most of the world after being infected with chickenpox you are immune for life unless it evolves into shingles which is a similar but very different mutation than this one still being driven by natural selection like this. This Synthetic Gene of chickenpox is to be used in Retroviral Vectors for gene therapy as a special Chickenpox caspid that has a extended carrying capacity being a combination of 3 chickenpox caspid genes each with a 100,000 to 160,000 bp carrying capacity.

 

 


Edited by VictorMedvil, 03 September 2019 - 10:54 PM.


#13 VictorMedvil

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Posted 28 August 2019 - 05:53 AM

Further, the Next Project within V.E.C.T.O.R., Early 2017

 

Name:  Extremophillic Chimeric Phagepox MV-5

 

Type: Multi-valent Controlled Evolved Extremophile Chimeric bacteriophage/chickenpox

 

Status:Created,Model tested by Protein Folding and Viral Structural Simulation, Method of Synthesis DNA recombination and Directed Evolution.

 

Gene Map 

New-Bitmap-Image-2.png

 

Culture Picture

WIN-20190828-07-40-10-Pro.jpg

 

Thoughts: This was a Bacteriophage Chickenpox chimeric creation to attempt to construct another synthetic gene which was successful the Caspid of Bacteriophages is between 100,000 and 200,000 bp to carry their long genome while chickenpox is also has a carrying capacity of between 100,000 and 160,000 bp thus the idea was combining Bacteriophages with chickenpox would yield a caspid that was able to carry a capacity of DNA or RNA beyond 200,000 bp, the chimera was successful between 3 bacteriophages and 2 variants of chickenpox so there is definately a caspid carrying all the DNA so I would suspect that the carrying capacity of this new chimeric caspid being between 500,000 and 1,000,000 bp, the MV-5 itself is not necessarily dangerous but is still a exotic pathogen being BSL-2 which will cause viral inflammation of infected areas of the body which will go away within hours being the only bad symptom of this chimeric pathogen while still killing bacteria even gut bacteria that are good for the body. This has a bright beige color in and out of light showing once again it is a successful chimera between multiple organisms as none of the virii are naturally beige in color. This being like the Bacteriophage MV-3 but having the Cyrophile and Thermophile chickenpox virii merged into the genome of this organism which is probably what gives the these virii this color of beige. This being produced by the producer Machine Bacteria used in the MV-3 Phage, I have always wanted to look at these virii under a electron microscope to see what they actually look like but have never had the chance to see what Phagepox MV-5 looks like.

 

 

It's a amazing thing to me the feedback loop between mutation, Artificial selection, and DNA recombination never really ends...... Infinitely producing synthetic genes like a gene machine, that is the essence of directed evolution.


Edited by VictorMedvil, 04 September 2019 - 12:02 AM.


#14 VictorMedvil

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Posted 31 August 2019 - 06:31 AM

Furthermore, the Next Project within V.E.C.T.O.R., Mid 2018

 

Name:  N-Targeting Extremophillic Extended Retroviral Vector

 

Type: Uni-valent Pseudo-typed Synthetic Retroviral Vector

 

Status: Never Created,Model tested by Protein Folding, Viral Structural Simulation, and Directed Evolution, Awaiting Synthesis

 

Gene Map

N-Targetting-Extremophillic-Extended-Ret

 

Thoughts: This was a vector using the Chickenpox MV-3's synthetic capsid which I thought would make a larger carrying capacity of 100,000 to 160,000 bp for gene delivery which I capped at 90,000 bp for legal reasons. This is a different caspid used for a more basic retroviral vector which has also been pseudo-typed for entry to every cell in the human body, I was going to construct this in 2018-2019 under West Nanorobotics  if I had a buyer for this vector which undoubtedly works, I am almost 100% certain that this vector works without creating it. This a combination of 3 different viruses however is not a MV series as it does not have multiple glycoproteins, this is starting a new type of synthetic vectors which also can be MV as well but the envelope structure but a VSV-G gene was used instead for targeting every cell. The Chickenpox Capsid being used is much the same as Gag in structure which sits inside the envelope, the machinery of HIV-1 is still used as the pol gene is present which makes for a very large and efficient Lysogenic transfer of genes much like that of a Standard Retroviral Vector.


Edited by VictorMedvil, 03 September 2019 - 10:55 PM.


#15 VictorMedvil

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Posted 31 August 2019 - 06:57 AM

Furthermore, the Next Project within V.E.C.T.O.R., Late 2018

 

Name:   Extremophillic Extended Retroviral Vector MV-5

 

Type: Multi-valent Pseudo-typed Synthetic Retroviral Vector

 

Status: Never Created,Model tested by Protein Folding, Viral Structural Simulation, and Directed Evolution, Awaiting Synthesis

 

Gene Map

DUNh1Wp.png

Thoughts: This was a change in caspid of the other MV-5 Retroviral Vector to include the Synthetic Chickenpox MV-3 Caspid, this version has a carrying capacity of at-least 90,000 bp which could go up to 100,000 to 160,000 bp. This vector still targets Nerve,T-Cell,Liver,Lung,and Skin tissues only as the previous version of this vector which has a cas9 insert for CRISPR gene editing.


Edited by VictorMedvil, 03 September 2019 - 10:55 PM.


#16 VictorMedvil

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Posted 04 September 2019 - 12:18 AM

Previously, A Project within V.E.C.T.O.R. that I had forgotten, Late 2017

 

Name:   Metamorphic Genetic Warfare Agent MV-5

 

Type: Multi-valent Metamorphic coded Virus

 

Status: Never Created,Model tested by Protein Folding and Viral Structural Simulation

 

Gene Map

Zu0ki00-gif-1e80778e557ec7199671e1870316

 

Gene Map with Metamorphism

Zu0ki00-gif-1e80778e557ec7199671e1870316

 

Thoughts: In Late 2017, The US lifted bans on Gain of function research involving Hostile Pathogens this was a result of that I wanted to gain knowledge about Metamorphism of Biological organisms. This Metamorphic virus would within 45 second kill a mammal with the genes for a Nerve Agent and Necrosis encoded within the virus. The nature of metamorphism within this virus are the cut sequences required for the multi-valence and hostile genes to work which are done by Cas9, This vector has caspid size issues as all the hostile vectors which have been posted on purpose, The Golden Arrows indicate a gene disruption activator cut site, which makes the virus metamorph into a different state reproducing differently after the guide RNA has activated via Cas9 the Metamorphism of the Metamorphic Virus to this secondary state.


Edited by VictorMedvil, 04 September 2019 - 12:21 AM.


#17 VictorMedvil

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Posted 04 September 2019 - 12:59 AM

This Concludes the V.E.C.T.O.R. Projects after this a new form of organism was created called Metamorphic Organisms no longer being from the same kingdom all of the Organism's proteins that were used, then instead of just Virus proteins as in the previous examples which became obsolete in the terms of futuristic organisms research while still being useful then it became about hybrids between kingdoms and code structuring like computer programs. These New Pathogens and Vectors no longer being considered Virii but rather something else entirely a type of synthetic organism in 2019, the viral structure still being highly useful. For the Updated Designs for metamorphic organisms refer to (http://www.sciencefo...ellular-pastes/ and http://www.sciencefo...c-gel-infected/).

 

156758034819004224.jpg


Edited by VictorMedvil, 04 September 2019 - 08:38 PM.