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We tested whether the ProteinMPNN-redesigned BoNT/E variants could be combined with PACE-evolved mutations by grafting the 16 PACE mutations of E(4130)A2 into the top redesigned BoNT/E backgrounds D1, D2 and D3 (Fig

In hopes of developing drugs that could block viral entry, Genwei Zhang, a postdoc in Pentelutes lab, performed computational simulations of the interactions between the ACE2 receptor and the receptor binding domain of the coronavirus spike protein

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