Li Wan-Lu, Head-Gordon Teresa
Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Kenneth S. Pitzer Center for Theoretical Chemistry, University of California Berkeley, Berkeley, California 94720, United States.
ACS Cent Sci. 2021 Jan 27;7(1):72-80. doi: 10.1021/acscentsci.0c01556. Epub 2020 Dec 19.
As biocatalysts, enzymes are characterized by their high catalytic efficiency and strong specificity but are relatively fragile by requiring narrow and specific reactive conditions for activity. Synthetic catalysts offer an opportunity for more chemical versatility operating over a wider range of conditions but currently do not reach the remarkable performance of natural enzymes. Here we consider some new design strategies based on the contributions of nonlocal electric fields and thermodynamic fluctuations to both improve the catalytic step and turnover for rate acceleration in arbitrary synthetic catalysts through bioinspired studies of natural enzymes. With a focus on the enzyme as a whole catalytic construct, we illustrate the translational impact of natural enzyme principles to synthetic enzymes, supramolecular capsules, and electrocatalytic surfaces.
作为生物催化剂,酶具有高催化效率和强特异性的特点,但由于其活性需要狭窄且特定的反应条件,因而相对脆弱。合成催化剂提供了在更广泛条件下实现更多化学多样性的机会,但目前尚未达到天然酶的卓越性能。在此,我们基于非局部电场和热力学涨落的作用,通过对天然酶的仿生研究,探讨一些新的设计策略,以改进任意合成催化剂的催化步骤和周转率,从而加速反应速率。我们聚焦于作为整体催化结构的酶,阐述天然酶原理对合成酶、超分子胶囊和电催化表面的转化影响。