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Designing Artificial Metalloenzymes by Tuning of the Environment beyond the Primary Coordination Sphere

化学 协调球 小学(天文学) 合理设计 纳米技术 模板 异核分子 配位复合体 组合化学 生化工程 金属 立体化学 有机化学 核磁共振波谱 材料科学 物理 工程类 天文
作者
Casey Van Stappen,Yunling Deng,Yiwei Liu,Hadi Heidari,Jingxiang Wang,Zhou Yu,Aaron P. Ledray,Yi Lu
出处
期刊:Chemical Reviews [American Chemical Society]
卷期号:122 (14): 11974-12045 被引量:81
标识
DOI:10.1021/acs.chemrev.2c00106
摘要

Metalloenzymes catalyze a variety of reactions using a limited number of natural amino acids and metallocofactors. Therefore, the environment beyond the primary coordination sphere must play an important role in both conferring and tuning their phenomenal catalytic properties, enabling active sites with otherwise similar primary coordination environments to perform a diverse array of biological functions. However, since the interactions beyond the primary coordination sphere are numerous and weak, it has been difficult to pinpoint structural features responsible for the tuning of activities of native enzymes. Designing artificial metalloenzymes (ArMs) offers an excellent basis to elucidate the roles of these interactions and to further develop practical biological catalysts. In this review, we highlight how the secondary coordination spheres of ArMs influence metal binding and catalysis, with particular focus on the use of native protein scaffolds as templates for the design of ArMs by either rational design aided by computational modeling, directed evolution, or a combination of both approaches. In describing successes in designing heme, nonheme Fe, and Cu metalloenzymes, heteronuclear metalloenzymes containing heme, and those ArMs containing other metal centers (including those with non-native metal ions and metallocofactors), we have summarized insights gained on how careful controls of the interactions in the secondary coordination sphere, including hydrophobic and hydrogen bonding interactions, allow the generation and tuning of these respective systems to approach, rival, and, in a few cases, exceed those of native enzymes. We have also provided an outlook on the remaining challenges in the field and future directions that will allow for a deeper understanding of the secondary coordination sphere a deeper understanding of the secondary coordintion sphere to be gained, and in turn to guide the design of a broader and more efficient variety of ArMs.

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