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探索酶调节剂的肽空间。

Exploring peptide space for enzyme modulators.

机构信息

Center for Single Molecule Biophysics, Arizona State University, Tempe, Arizona 85287, USA.

出版信息

J Am Chem Soc. 2010 May 12;132(18):6419-24. doi: 10.1021/ja100403a.

Abstract

A method is presented for screening high-density arrays to discover peptides that bind and modulate enzyme activity. A polyvinyl alcohol solution was applied to array surfaces to limit the diffusion of product molecules released from enzymatic reactions, allowing the simultaneous measurement of enzyme activity and binding at each peptide spot. For proof of concept, it was possible to identify peptides that bound to horseradish peroxidase, alkaline phosphatase, and beta-galactosidase and substantially altered enzyme activity by comparing the binding level of peptide to enzyme and bound enzyme activity. This basic technique may be generally applicable to find peptides or other small molecules that modify enzyme activity.

摘要

本文提出了一种筛选高密度阵列以发现结合并调节酶活性的肽的方法。将聚乙烯醇溶液施加到阵列表面以限制从酶反应释放的产物分子的扩散,从而可以同时测量每个肽点的酶活性和结合。为了验证这一概念,通过比较肽与酶的结合水平和结合酶活性,有可能鉴定出与辣根过氧化物酶、碱性磷酸酶和β-半乳糖苷酶结合并显著改变酶活性的肽。这种基本技术可能普遍适用于发现修饰酶活性的肽或其他小分子。

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