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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Baric's hACE2 transgenic mice were shared with the WIV for GOF like virus experiments designed to "assess" the potential for coronaviruses to jump from animals to humans.
2. Baric spills his humanized mice beans to Father Racaniello during a heart rending TWIV confessional in March 2020, admitting he sent his hACE2 mice to WIV in 2018 (as part of the infamous NIAID grant mentioned above):
"Our R01 work shows that bats in South China harbor many SARSr-CoVs (50+), some of which are able to use human ACE2 to enter human cells, infecting humanized mouse models to cause SARS-like illness, and evade available therapies or vaccines"
@breakfast_dogs @gadboit @NLink247 1. Insect cell baculovirus cell cultures become contaminated with insect genomic material. 2. Replication process can lead to presence of viral DNA & cellular components in culture medium. 3. This LEADS to contamination of viral product with baculovirus & insect cell-derived DNA.
@breakfast_dogs @gadboit @NLink247 Contamination
4. Expression of SC-2 Spike RBD Using the Insect Cell-Baculovirus System