High-throughput screening of enzyme inhibitors: Automatic determination of light-binding inhibition constants

被引:55
作者
Kuzmic, P
Sideris, S
Cregar, LM
Elrod, KC
Rice, KD
Janc, JW
机构
[1] BioKin Ltd, Madison, WI 53708 USA
[2] Axys Pharmaceut Inc, Dept Med Chem, San Francisco, CA 94080 USA
[3] Axys Pharmaceut Inc, Dept Enzymol, San Francisco, CA 94080 USA
关键词
enzyme kinetics; mathematics; data analysis; statistics; tight binding; inhibition constant; high-throughput screening; mast-cell tryptase;
D O I
10.1006/abio.2000.4501
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Determination of tight-binding inhibition constants by nonlinear least-squares regression requires sufficiently good initial estimates of the best-fit values. Normally an initial estimate of the inhibition constant must be provided by the investigator. This paper describes an automatic procedure for the estimation of tight-binding inhibition constants directly from dose-response data. Because the procedure does not require human intervention, it was incorporated into an algorithm for high-throughput screening of enzyme inhibitors. A suitable computer program is available electronically (http://www.biokin.com). Representative experimental data are shown for the inhibition of human mast-cell tryptase. (C) 2000 Academic Press.
引用
收藏
页码:62 / 67
页数:6
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