A single line often inverts meaning once you see what it
answers, so neighbouring messages are always shown.
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Probably more 'immune' related than 'mouse' related?
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Yeah - the fact these are epitopes to me strongly suggests immune selection - mouse or human. But I think that the particular substitution may depend on the species. Analysis coming...:sunglasses:
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https://jvi.asm.org/content/82/14/6984 Relevant paper: "They show that the major species barriers are determinedby interactions between four ACE2 residues (residues 31, 35, 38, and 353) and two RBD residues (residues 479and 487), that early civet SARS-CoV isolates were prevented from infecting human cells due to imbalanced saltbridges at the hydrophobic virus/receptor interface, and that SARS-CoV has evolved to gain sustained infectivity for human cells by eliminating unfavorable free charges at the interface through stepwise mutations at positions 479and 487."
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The equivalent amino acids to SC1 479 and 487 in terms of alignment to RBD appear to me to be 493 and 501, but Ineed to really take a closer look at ALL the structures.
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2020-12-22 08:52
Robert F. Garry
Those are the same and it's the alignment in PO1.
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SC1 479 and SC2 493 interact with ACE2 similarly - however SC1 487 and SC2 501 interactions with ACE2 are completely different... *Correction - not completely different - just different*
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The pattern of prolines in SC1 and SC2 RBDs are distinct - look at PO1 - which creates a very different interaction with ACE2 - but we're seeing in real time the adaptation of SC2 to receptors in humans, minks and mice pretty muchas you'd draw it up. The twist that it may be immune selection driving better receptor binding is not expected at leastby me. Tuning up receptor binding affinity happened in SARS1 per the JVI paper above, but more subtle and [probably?] not an immune component there in 2002 and 2005.
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Interesting difference between SC1 and SC2 is that it was pretty darn quick in the former - essentially happened right after the jump from intermediate hosts. Slower for SC2, but it's probably because it was pretty darn good atbinding already.
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Yeah, so this "We present evidence that the Spike H69/V70 is a fitness enhancing change that may be stabilising other S gene mutations" from Gupta's recent preprint is what worries me the most and I'm wondering if E484K (or N417K) could play a similar role in the SA lineage that H69/V70 is playing in the UK lineage. Add Nelly on top ofthat, and you might end up with what we're observing now.