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Catalytic role of enzymes Short strong H-bond-induced partial proton shuttles and charge redistributions

机译:酶的催化作用短的强H键诱导的部分质子穿梭和电荷重新分布

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摘要

A two-step reaction mechanism (catalyzed alternatively by acid and base) with partial proton shuttles and charge redistributions promoted by short strong H bonds (SSHBs) (playing a dual role as an amphi-acid/base catalyst) is proposed to explain the enormous rate enhancement observed in enzymatic reactions involving carbanion intermediates. The SSHBs in the two-step reactions are found to be responsible for enhancing enzyme- substrate interactions in favor of the transition state structure over that of reactant. The detailed quantum theoretical studies of ketosteroid isomerase provide evidence of assisting roles of SSHB in enzymatic activity. The understanding of the two-step reaction mechanism would be a useful aid in designing novel functional enzymes and abzymes.
机译:提出了两步反应机制(由酸和碱交替催化),具有部分质子穿梭和由短的强氢键(SSHBs)促进的电荷再分布(起两性酸/碱催化剂的双重作用),以解释这一巨大的作用。涉及碳负离子中间体的酶促反应中速率增加。发现两步反应中的SSHB负责增强酶-底物的相互作用,从而使过渡态结构优于反应物。酮类固醇异构酶的详细量子理论研究提供了SSHB在酶活性中辅助作用的证据。对两步反应机理的理解将有助于设计新型功能酶和抗体酶。

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