Artificial Metalloenzymes and Metallopeptide Catalysts for Organic Synthesis

被引:216
|
作者
Lewis, Jared C. [1 ]
机构
[1] Univ Chicago, Dept Chem, Searle Chem Lab, Chicago, IL 60637 USA
来源
ACS CATALYSIS | 2013年 / 3卷 / 12期
基金
美国国家科学基金会;
关键词
artificial metalloenzymes; metallopeptide; molecular recognition; evolution; catalysis; ASYMMETRIC TRANSFER HYDROGENATION; BIOTIN-AVIDIN TECHNOLOGY; CARBONIC-ANHYDRASE-II; DUAL ANCHORING STRATEGY; SOLID-PHASE SYNTHESIS; ALPHA-AMINO-ACIDS; DE-NOVO DESIGN; ENANTIOSELECTIVE CATALYSIS; PEROXIDASE-ACTIVITY; DIRECTED EVOLUTION;
D O I
10.1021/cs400806a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transition metal catalysts and enzymes possess unique and often complementary properties that have made them important tools for chemical synthesis. The potential practical benefits of catalysts that combine these properties and a desire to understand how the structure and reactivity of metal and peptide components affect each other have driven researchers to create hybrid metal-peptide catalysts since the 1970s. The hybrid catalysts developed to date possess unique compositions of matter at the inorganic/biological interface that often pose significant challenges from design, synthesis, and characterization perspectives. Despite these obstacles, researchers have developed systems in which secondary coordination sphere effects impart selectivity to metal catalysts, accelerate chemical reactions, and are systematically optimized via directed evolution. This perspective outlines fundamental principles, key developments, and future prospects for the design, preparation, and application of peptide- and protein-based hybrid catalysts for organic transformations.
引用
收藏
页码:2954 / 2975
页数:22
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