Why would this purification procedure be applied to RaTG13’s sample but not any of the other samples of the same type and uploaded around the same time?
2. Mutations in the Spike protein of RaTG13
This recent paper argues that mutation from T to R at position 403 in RaTG13’s spike is essential for allowing it to infect human cells:
Spike residue 403 affects binding of coronavirus spikes to human ACE2
Logically therefore, were "they" to generate a consensus sequence virus (even within the RsYN06-RaTG13 clade) as has been suggested by some, it would surely have an R at that position...
Position 403
Without knowing what "they" have (or "had") in their dearly missed database, which may have been used to generate a consensus sequence, we can’t know what sequence it would produce.
but we can be reasonably sure that it would have an R, not a T at position 403...
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1. The long awaited 293 questions for Dr. Ralph Baric have finally been completed and shared! Long live the quest for truth! You are hereby invited to read the sharpest, most lethal 293-question dossier ever built.
1. "These tiny fragments were far smaller than cells and even smaller than many viruses. Some were close to the size of DNA strands. Under high magnification, she noticed small hooked shapes with sharp points.
✴️2. OVERLOOKED
"She realized that the plastic in human brains was not only present, but surprisingly small. The fragments were so tiny that common diagnostic tools could not detect them. Pathologists had likely been overlooking them for years."
"The two original samples showed a strong link between plastic particles and dementia. As Bearer expanded her work to ten more donated brains, she found plastic in every single one. None were free of synthetic fragments."
Unfortunately, there is no direct proof provided by Redfield in this new interview, but he cites engineering features, early data, and classified information.
🧵3. Summary of Redfield's Statements
(on SARS-CoV-2 Origins & Cover-Up)
He claims SARS-CoV-2 originated from GOF research in a lab and emphasizes a significant US role alongside China.
He views this as a major biosecurity failure with ongoing suppression of transparency.
"Of note, the spike protein of this novel bat coronavirus possesses a functional FCS at the S1/S2 junction with a unique amino acid sequence motif (RDAR) that differs from that found in SARS-CoV-2 (RRAR) by only 1 amino acid."
"The molecular biology capabilities of WIV & the genome assessment are consistent with the hypothesis that SARS-CoV-2 was a lab-engineered virus that was part of a bank of chimeric viruses in Zheng-Li Shi's laboratory at WIV that escaped from containment"
Between 2017 and 2019, WIV created full-length a infectious clone in pBAC-CMV using an unpublished bat Coronavirus genome as template (BatCoVX)
page 85
3. Hypothesis 3:
Between 2017 and 2019, WIV created chimeric Bat-CoV-X viruses using the pBACCMV-BCOVX backbone and swapping out key cassettes with other bat Coronaviruses (RBD, RBM, etc.) and adding additional features such as a furin cleavage site