Time Innovation-Understanding mRNA Sequence Design and Its Dangers-from GROK (Free)

From my study of RNA sequencing over 6 years and working with the Harmonic for 35, my comments are in parentheses.

Can they do it to tRNA? It matters to my project because I will not allow it to be misused.

Geneticists and molecular biologists manipulate mRNA by designing synthetic sequences that can be introduced into cells to produce specific proteins. Here’s a simplified rundown of how it works, based on what’s widely known:

  1. Sequence Design: They start by identifying the target protein—say, the spike protein of a virus like SARS-CoV-2. Using the genetic code, they reverse-engineer an mRNA sequence that codes for that protein. This is done computationally, optimizing the sequence for stability and efficient translation in human cells. (THIS IS BAD.)
  2. Chemical Modifications: Natural mRNA breaks down quickly in the body, so they tweak it. For example, they replace uridine with modified nucleotides like pseudouridine. This makes the mRNA less likely to trigger an immune overreaction and more stable, giving it time to do its job. (NOPE. IT KILLED PEOPLE.)
  3. Synthesis: The designed mRNA is then synthesized in a lab using enzymes like T7 RNA polymerase, which builds the RNA strand from a DNA template. This is a controlled, industrial-scale process for things like vaccines.
  4. Delivery: To get the mRNA into cells, it’s packaged in lipid nanoparticles—tiny fat bubbles that protect the mRNA and help it slip through cell membranes. Once inside, the cell’s own machinery reads the mRNA and churns out the protein. (NANOTECH is very bad, dangerous, and illegal in the military to have it in your body.)
  5. Control Elements: They also add bits like a 5’ cap and a poly-A tail to the mRNA. These act like start and stop signals, (fake Methionine and Stop Codons, Red Moon and Yellow Sun.) ensuring the mRNA gets translated properly and doesn’t degrade too fast.

For vaccines, the result is that your cells temporarily produce the target protein (e.g., the viral spike), your immune system spots it, and you build immunity—all without ever seeing the actual virus. The mRNA itself doesn’t stick around; it degrades naturally after a short time.

This is pure evil IMO.

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