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用于蛋白质功能大规模分析的筛选和选择方法。

Screening and selection methods for large-scale analysis of protein function.

作者信息

Lin Hening, Cornish Virginia W

机构信息

Department of Chemistry, Columbia University, New York, NY 10027, USA.

出版信息

Angew Chem Int Ed Engl. 2002 Dec 2;41(23):4402-25. doi: 10.1002/1521-3773(20021202)41:23<4402::AID-ANIE4402>3.0.CO;2-H.

Abstract

High-throughput assays hold tremendous promise for protein engineering and proteomics. With powerful assays it should be possible to evolve, for example, a stereoselective esterase for the chemical synthesis or a site-specific endonuclease for biomedical research. Entire cDNA libraries, which encode all of the proteins expressed in a given organism or cell line, should simply be passed through a battery of biochemical assays to determine the function of each individual protein. Herein we look at the types of assays that have been developed and how close we are to our goals of engineering proteins with new activities as well as rapidly assigning function to the thousands of proteins that make up each genome.

摘要

高通量检测技术在蛋白质工程和蛋白质组学领域有着巨大的应用前景。借助强大的检测技术,例如,有可能开发出用于化学合成的立体选择性酯酶或用于生物医学研究的位点特异性核酸内切酶。完整的cDNA文库编码了特定生物体或细胞系中表达的所有蛋白质,只需通过一系列生化检测,就能确定每个蛋白质的功能。在本文中,我们将探讨已开发的检测类型,以及我们距离实现利用新活性设计蛋白质的目标有多近,同时也将探讨能否快速为构成每个基因组的数千种蛋白质赋予功能。

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