Spike Protein, Gain of Function, and Why mRNA Injections Aren't Vaccines

What Is the Spike Protein?

The Spike protein is a surface protein present naturally in several viruses, including coronaviruses. But SARS-CoV-2's Spike is different. It was manufactured through Gain of Function (GoF) research. That means it's not a natural protein.

Figure 1: Structure of SARS-CoV-2 showing the Spike protein highlighted on the viral surface. The Spike protein is a surface protein naturally present in coronaviruses, but SARS-CoV-2's version was manufactured through Gain of Function research with 4 major modifications: enables human transmission, increases pathogenicity, allows persistence in the organism, and creates unprecedented biological functions.

GoF introduced 4 major modifications:

1. Transmission: Enables a virus of animal origin to infect humans
2. Increased pathogenicity: Potentially makes the virus more dangerous
3. Persistence: Allows the virus to remain in the organism longer
4. Unprecedented functions: Creates biological capabilities not seen in nature

This isn't random evolution. It's engineering.

Spike Structure: Engineered to Infect Humans

The Spike protein is composed of 3 identical units. Here's what makes it dangerous:

Figure 1a: Detailed molecular model of the SARS-CoV-2 Spike protein showing the 3 identical units. Red arrows indicate the 3 Gp120 inserts from HIV that enable binding to human ACE2 receptors. Green arrow shows the Furin Cleavage Site unique to SARS-CoV-2.

HIV Inserts

Three Gp120 inserts from HIV are perfectly adapted to bind to human ACE2 receptors. That's why the virus infects humans so effectively. Without these inserts, zoonotic transmission (animal-to-human) wouldn't work this efficiently.

Furin Cleavage Site (FCS)

The FCS is present only in SARS-CoV-2. No other coronavirus has it. This site allows the Spike to split into two subunits:

S1 subunit:

• Amyloid formation
• Neuroinflammatory effects

S2 subunit:

• Fusogenic (fusion with cells)

The Translation: The Spike isn't just a key that unlocks cells. It's a bioweapon with two separate attack mechanisms. One for your brain, one for cell fusion.

How Proteins Are Made (The mRNA Injection Mechanism)

Your cells produce proteins through two steps:

Figure 2: Dr. Anthony Fauci and NIAID's role in funding Gain of Function research on coronaviruses at the Wuhan Institute of Virology, leading to the engineered Spike protein of SARS-CoV-2.

1. Transcription DNA (genes) gets transcribed into mRNA

2. Translation The mRNA gets translated into proteins. These are specific sequences of amino acids.

Each protein has a biological function, like a key opening a lock. The Spike of SARS-CoV-2 is the key that allows viral entry.

How SARS-CoV-2 Infects Cells

SARS-CoV-2 is an obligate cellular parasite. It needs your cellular machinery to multiply:

Figure 3: Mechanisms of infection by SARS-CoV-2. Like all viruses, SARS-CoV-2 is an obligate cellular parasite requiring the cell's machinery to multiply. The Spike (key) binds to ACE2 receptor (lock), virus fuses and penetrates, viral mRNA is released and translated by cell tools to produce viral proteins (N, S, M, E), virions assemble, then cell explodes releasing virions to infect other cells.

1. Spike (key) binds to ACE2 receptor (lock)
2. Virus fuses and penetrates the target cell
3. Viral mRNA is released
4. Your cell's tools translate the viral mRNA to produce viral proteins (N, S, M, E)
5. Viral proteins assemble into new virions
6. Cell explodes, releasing virions to infect other cells

The "Vaccine" Bait and Switch

Following infection, your cells produce Spike. That's expected.

But following mRNA or DNA injections, your cells also produce Spike. These injections work the same way. They force your body to manufacture the antigen.

The problem: These products were wrongly called "vaccines."

Why? Because they don't meet the definition.

What Is a Vaccine? (Actual Definition)

The aim of a vaccine: Use material harmless to the organism to mimic pathogen infection. This allows immune defense development (antibodies), inducing lasting protection against future encounters and preventing illness.

How real vaccines work:

• Inject attenuated or inactivated pathogen
• Or inject purified antigen from that pathogen
• Known quantity = known dose

Key point: Vaccines are prophylaxis (prevention), not curative treatment.

They Changed the Definition Instead of Fixing the Product

In September 2021, the CDC and Merriam-Webster updated their definitions of vaccine and vaccination.

Old CDC definition (before Sept 2021): A product that stimulates a person's immune system to produce immunity to a specific disease, protecting the person from that disease.

New CDC definition (Sept 2021): A preparation that is used to stimulate the body's immune response against diseases.

What changed: Immunity became protection Protecting the person from that disease was removed entirely

The CDC's excuse: They claimed the change was for transparency and technical accuracy to avoid implying vaccines are 100% effective.

The reality: They moved the goalposts. When your product doesn't meet the definition, you change the definition.

This definition was changed to accommodate products that:

• Don't provide lasting immunity
• Don't prevent infection
• Don't prevent transmission
• Require endless boosters

The word vaccine used to mean something specific. Now it means whatever they need it to mean.

Why mRNA Injections Aren't Vaccines

mRNA injections work by injecting genetic code (DNA or RNA) that makes your body produce the antigen. That antigen is the Spike protein.

Three problems:

1. We don't know which cells produce Spike
2. We don't know the quantity produced
3. We don't know how long production continues

These are genetic injections, not vaccines.

The biological reality: In natural infection, the Spike protein doesn't produce the most antibodies or the most lasting ones. Basing supposedly protective injections on this single toxic protein was nonsense.

Viral Spike vs mRNA Spike: What's Different?

Nearly identical. But there are 3 critical exceptions:

1. Amino Acid Substitutions

The mRNA-coded Spike has 2 amino-acid substitutions (986-987) that create unknown conformational changes.

2. Different Glycosylation

The mRNA Spike has different sugar molecules attached, affecting how it interacts with cells.

3. N-methyl-pseudouridines

The mRNA uses N-methyl-pseudouridine instead of natural uridine.

What this means:

• Causes reading errors during protein synthesis
• Potential carcinogenic effects
• Unknown long-term consequences

What stays the same:

• Furin cleavage site is conserved → S1/S2 dissociation still happens
• Same ACE2 interaction → still infects human cells

Bottom line: The mRNA Spike is engineered differently with potentially MORE dangerous properties than the natural viral Spike.

Lipid Nanoparticles (LNPs): The Delivery System

LNPs carry the mRNA code. They're another problematic component:

Figure 5: Biodistribution of Lipid Nanoparticles (LNPs). The modified mRNA sequence coding for Spike protein is encapsulated in LNPs (fats) for protection because mRNA is fragile. These LNPs have demonstrated inflammatory properties, improve distribution and cellular integration, are not vectorized (can reach all cells), and cross essential biological barriers including the blood-brain barrier and placenta. Moderna patented this formulation in 2012 (WO2012045075 A1, European patent EP11830061).

What they do: The modified mRNA sequence coding for the Spike protein must be protected because mRNA is fragile. For this, it has been encapsulated in lipid nanoparticles (LNPs), or fats. Yet it has been demonstrated that these LNPs have inflammatory properties.

These LNPs improve distribution in the organism and cellular integration. They are not vectorized and can therefore address all the cells of the body. Worse still, they allow the crossing of essential biological barriers that defend certain body compartments, such as the blood-brain barrier (which protects the brain) or the placenta (which protects the fetus).

Endosomal membrane damage:

LNPs cause endosomal membrane damage, contributing to:

• Neurodegenerative disease, including Alzheimer
• Cancer progression
• Exploitation by pathogens to enhance infectivity

Sources:

• https://doi.org/10.1101/2024.04.16.589801
• https://link.springer.com/article/10.1186/s40035-024-00460-7
• https://link.springer.com/article/10.1007/s10555-020-09870-1
• https://link.springer.com/chapter/10.1007/978-0-387-39951-5_11

Moderna patent:

• International patent WO2012045075 A1 (2012)
• European patent EP11830061, registered the same year
• European Patent Register: https://register.epo.org/application?number=EP11830061

LNPs don't stay at the injection site. They distribute systemically. That means Spike production can happen anywhere. Including your brain and a developing fetus.

SV40 Promoter: The Nuclear Key

Pfizer's mRNA injections contain something else problematic: SV40 promoter sequences.

Figure 6: SV40 promoter sequence found in Pfizer mRNA injections. SV40 (Simian Virus 40) is a virus known to cause cancer in animal models. The promoter sequence acts as a nuclear localization signal, helping mRNA enter the cell nucleus and enabling potential integration into human DNA, which would turn cells into permanent Spike protein factories.

What is SV40? Simian Virus 40. A virus known to cause cancer in animal models.

What does the promoter do?

• Acts as a nuclear localization signal
• Helps mRNA enter the cell nucleus
• Enables potential integration into human DNA

Why this matters: If mRNA integrates into your genome, your cells become permanent Spike factories. This isn't temporary. This isn't what vaccines do.

Dr. Meryl Nass Confirms: Not Vaccines

Dr. Meryl Nass, internist and researcher, testified before Congress:

Her conclusions:

• These injections are not vaccines
• LNPs are problematic
• mRNA technology gives unknown dose, duration, and cells producing Spike
• Injections based on the most toxic (not most immunogenic) protein
• Several viral proteins are synthetic and designed to harm the immune system

Her statement:

"I think this virus was made in a biological weapons laboratory. It was designed to be particularly toxic."

Are These Biological Weapons?

Figure 7: Professor Francis Boyle's affidavit (May 27, 2024) confirms both the SARS-CoV-2 virus and the mRNA injections meet the legal definition of biological weapons and weapons of mass destruction. Boyle drafted the U.S. Biological Weapons Anti-Terrorism Act of 1989.

The evidence suggests yes.

Congressional Hearings

U.S. Congressional and Senate hearings since May 2021 investigated virus origin and GoF funding using FOIA requests. These bipartisan hearings revealed:

• Major corruption and cover-ups by government agencies
• GoF funding at Wuhan Institute
• Lies under oath by key officials
• Involvement of multiple countries

Key witnesses:

• Dr. Peter Daszak (EcoHealth)
• Dr. Anthony Fauci (NIAID)
• Dr. David Morens

Senator Rand Paul hearings:

• 4 scientists testified
• Revealed obstruction of lab-origin papers
• Dangerous GoF research exposed
• Proposal for new oversight law (rejected for now)

Prof. Francis Boyle's Affidavit

Prof. Francis Boyle's affidavit (May 27, 2024):

Both the virus and the mRNA injections meet the legal definition of:

• Biological weapons
• Weapons of mass destruction

Boyle's credentials:

• Drafted the U.S. Biological Weapons Anti-Terrorism Act of 1989
• Expert in biological weapons law
• Professor of international law

His findings:

• DARPA (Pentagon) funded Moderna mRNA technology
• Fort Detrick was involved
• Both virus and vaccines are biological weapons
• This meets the legal definition of WMDs

U.S. Military Involvement

Figure 8: Comprehensive diagram showing the web of connections between U.S. agencies (NIH/NIAID, DARPA, Department of Defense), research organizations (EcoHealth Alliance, Moderna), international partners (Wuhan Institute, France), and funding sources involved in Gain of Function research that led to SARS-CoV-2. Originally published by BAM! in June 2024.

The connection web:

• NIH/NIAID funded GoF research
• EcoHealth funneled money to Wuhan
• Moderna received DARPA funding
• Military involvement at multiple levels
• Multiple countries involved
• No one spends millions on a "cold" without return on investment

The reality: GoF research = disguised biological weapons research, funded by U.S. intelligence/military.

Proof of U.S. funding bio-research in Ukraine since 2005:

• Including Metabiota
• Hunter Biden connections
• Treaty evidence available

The Spike Protein Is the Biological Weapon

Common to virus and injections:

The Spike protein is the most toxic protein, responsible for:

• Vascular damage
• Cardiotoxicity
• Neurotoxicity
• Autoimmunity
• Cancer reactivation
• Amyloid/prion-like diseases
• And more...

U.S. Patent — Modified polynucleotides for oncology-related proteins (Moderna):

Figure 9: Moderna patent US-9587003-B2, filed in 2012 and granted in 2016. The patent document shows multiple biological activities explained by the furin cleavage site, demonstrating intent and foreknowledge of the Spike protein's engineered properties years before COVID-19. Sources: PubChem and Daily Mail

• 2016 patent (filed 2012)
• Shows multiple activities explained by the furin cleavage site
• Demonstrates intent and foreknowledge

The Bottom Line

What the evidence shows:

• Patent timeline demonstrates intent
• Virus + injections = military biological weapons (fragmentation + delayed effect)
• U.S. military involvement and cover-ups
• Multiple countries involved
• No one spends millions on a "cold" without return on investment

Many "emerging" pathogens raise the same questions:

• HIV
• Bird flu
• Zika
• Ebola
• Lyme disease

The biggest trauma: Governments may not have our best interests at heart. We must inform ourselves, organize, and collectively resist.

This is about the survival of humanity.

What Lessons Can We Draw?

What Should We Do?

Treat every new pathogen seriously. Especially non-natural ones.

Early treatment is the only sustainable option

Boost natural immunity

Use reliable sources for prophylaxis & treatment

Be responsible toward others if infected

Take Care of Your "Natural" Immunity

✓ Balanced diet ✓ Outdoor exercise (30 min/day, no mask) ✓ Quality sleep (away from screens) Daily supplementation if needed (Vit D, liposomal Vit C, Zinc). Especially over 65.

Prophylaxis

20+ molecules available without prescription (most also work for treatment)

Reliable sources:

• c19early.org (prophylaxis tab)
• Dr. Sabatier
• Dr. Zelenko

Main prophylactics:

• Vitamin D
• Vitamin C
• Zinc
• Quercetin
• Curcumin
• Nigella sativa
• Ravintsara essential oil
• Aspirin
• Probiotics
• Ivermectin
• Doxycycline

Summary

Spike protein:

• Engineered through Gain of Function
• Contains HIV inserts for human infection
• Splits into neuroinflammatory (S1) and fusogenic (S2) components
• mRNA version has carcinogenic modifications
• Spike IS the biological weapon

mRNA injections:

• Make your body produce the toxic Spike protein
• mRNA Spike has unknown conformational changes
• No dose control
• No duration control
• No tissue specificity (thanks to LNPs)
• SV40 promoters enable nuclear entry and potential genome integration

Vaccine definition requires:

• Known antigen
• Known dose
• Prophylactic purpose

mRNA injections meet none of these criteria. They're genetic modification tools and biological weapons marketed as vaccines.

Based on the presentation "Once upon a time the Spike, the Covid and the biological weapons…" by Dr. Typhaine Pinsolle, August 15, 2024.