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从底层设计酶:具有结构化肽外配位层的活性镍电催化剂。

Enzyme design from the bottom up: an active nickel electrocatalyst with a structured peptide outer coordination sphere.

机构信息

Pacific Northwest National Labs, Richland, WA 99354 (USA).

出版信息

Chemistry. 2014 Feb 3;20(6):1510-4. doi: 10.1002/chem.201303976. Epub 2014 Jan 17.

Abstract

Catalytic, peptide-containing metal complexes with a well-defined peptide structure have the potential to enhance molecular catalysts through an enzyme-like outer coordination sphere. Here, we report the synthesis and characterization of an active, peptide-based metal complex built upon the well-characterized hydrogen production catalyst Ni(P(Ph)2N(Ph))2 (P(Ph)2N(Ph)=1,3,6-triphenyl-1-aza-3,6-diphosphacycloheptane). The incorporated peptide maintains its β-hairpin structure when appended to the metal core, and the electrocatalytic activity of the peptide-based metal complex (≈100,000 s(-1)) is enhanced compared to the parent complex (Ni(P(Ph)2N(APPA))2; ≈50,500 s(-1)). The combination of an active molecular catalyst with a structured peptide provides a scaffold that permits the incorporation of features of an enzyme-like outer-coordination sphere necessary to create molecular electrocatalysts with enhanced functionality.

摘要

具有明确肽结构的催化肽金属配合物具有通过类似酶的外部配位层来增强分子催化剂的潜力。在这里,我们报告了一种基于肽的金属配合物的合成和表征,该配合物基于众所周知的制氢催化剂Ni(P(Ph)2N(Ph))2(P(Ph)2N(Ph)=1,3,6-三苯基-1-氮杂-3,6-二磷杂环庚烷)。当肽连接到金属核时,所包含的肽保持其β-发夹结构,并且基于肽的金属配合物的电催化活性(≈100,000 s(-1))与母体配合物相比得到增强(Ni(P(Ph)2N(APPA))2;≈50,500 s(-1))。将活性分子催化剂与结构肽结合在一起提供了一个支架,该支架允许引入类似酶的外部配位层的特征,这些特征对于创建具有增强功能的分子电催化剂是必要的。

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