Centre for High-Throughput Biology (CHiBi) and Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, B.C. V6T 1Z1, Canada.
Chembiochem. 2009 Nov 23;10(17):2704-15. doi: 10.1002/cbic.200900384.
Directed enzyme evolution has proven to be a powerful tool for improving a range of properties of enzymes through consecutive rounds of diversification and selection. However, its success depends heavily on the efficiency of the screening strategy employed. Fluorescence-activated cell sorting (FACS) has recently emerged as a powerful tool for screening enzyme libraries due to its high sensitivity and its ability to analyze as many as 10(8) mutants per day. Applications of FACS screening have allowed the isolation of enzyme variants with significantly improved activities, altered substrate specificities, or even novel functions. This review discusses FACS-based screening for enzymatic activity and its potential application for the directed evolution of enzymes, ribozymes, and catalytic antibodies.
定向酶进化已被证明是一种强大的工具,可通过连续几轮的多样化和选择来改善酶的一系列性质。然而,其成功在很大程度上取决于所采用的筛选策略的效率。荧光激活细胞分选(FACS)由于其高灵敏度和每天能够分析多达 10(8)个突变体的能力,最近已成为筛选酶文库的强大工具。FACS 筛选的应用允许分离出具有显著提高的活性、改变的底物特异性甚至新功能的酶变体。本文讨论了基于 FACS 的酶活性筛选及其在定向进化酶、核酶和催化抗体方面的潜在应用。