Reymond Jean-Louis, Babiak Peter
Department of Chemistry & Biochemistry, University of Berne, Freiestrasse 3, 3012 Berne, Switzerland.
Adv Biochem Eng Biotechnol. 2007;105:31-58. doi: 10.1007/10_2006_032.
Enzyme screening technology has undergone massive developments in recent years, particularly in the area of high-throughput screening and microarray methods. Screening consists of testing each sample of a sample library individually for the targeted reaction. This requires enzyme assays that accurately test relevant parameters of the reaction, such as catalytic turnover with a given substrate and selectivity parameters such as enantio- and regioselectivity. Enzyme assays also play an important role outside of enzyme screening, in particular for drug screening, medical diagnostics, and in the area of cellular and tissue imaging. In the 1990s, methods for high-throughput screening of enzyme activities were perceived as a critical bottleneck. As illustrated partly in this chapter, a large repertoire of efficient screening strategies are available today that allow testing of almost any reaction with high-throughput.
近年来,酶筛选技术取得了巨大进展,特别是在高通量筛选和微阵列方法领域。筛选包括对样品库中的每个样品单独进行目标反应测试。这需要酶分析方法来准确测试反应的相关参数,例如与给定底物的催化周转率以及对映选择性和区域选择性等选择性参数。酶分析在酶筛选之外也发挥着重要作用,特别是在药物筛选、医学诊断以及细胞和组织成像领域。在20世纪90年代,酶活性的高通量筛选方法被视为一个关键瓶颈。如本章部分所示,如今有大量高效的筛选策略可供使用,几乎可以对任何反应进行高通量测试。