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Using BpyAla to generate copper artificial metalloenzymes: a catalytic and structural study

E. Klemencic, Richard C. Brewster, Hafiz Saqib Ali, J. Richardson, Amanda G. Jarvis

2024Catalysis Science & Technology18 citationsDOIOpen Access PDF

Abstract

). Interestingly, despite using the same protein scaffold, different attachment strategies for Bpy at the same residue (Q111) led to a switch in the enantiopreference of the ArM. X-ray crystal structures of SCP_Q111CBpy and SCP_Q111BpyAla ArMs with bound Cu(ii) ions unveiled crucial differences in the orientation of the catalytic centre. Combining structural information, alanine scanning studies, and computational analysis shed light on the distinct active sites of the ArMs, clarifying that these active sites stabilise the nucleophilic substrate on different sides of the electrophile leading to the observed switch in enantioselectivity. This work underscores the importance of integrating structural studies with catalytic screening to unravel the intricacies of ArM behaviour and facilitate their development for targeted applications in biocatalysis.

Topics & Concepts

BioconjugationChemistryEnantioselective synthesisBiocatalysisCombinatorial chemistryNucleophileElectrophileCatalysisActive siteDirected evolutionResidue (chemistry)StereochemistryBiochemistryReaction mechanismGeneMutantCyclopropane Reaction MechanismsAsymmetric Hydrogenation and CatalysisMetalloenzymes and iron-sulfur proteins
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