Matrix-Based Activity Pattern Classification as a Novel Method for the Characterization of Enzyme Inhibitors Derived from High-Throughput Screening

被引:5
作者
Auld, Douglas S. [1 ]
Jimenez, Marta [1 ]
Yue, Kimberley [1 ]
Busby, Scott [1 ]
Chen, Yu-Chi [1 ,2 ]
Bowes, Scott [1 ]
Wendel, Greg [1 ]
Smith, Thomas [1 ]
Zhang, Ji-Hu [1 ]
机构
[1] Novartis Inst Biomed Res, Ctr Prote Chem, 250 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Natl Ctr Adv Translat Sci, Bethesda, MD USA
关键词
mode of inhibition; enzyme inhibitors; inhibitor classification; enzyme assays; FIREFLY LUCIFERASE; RNA-POLYMERASE; IDENTIFICATION; DISCOVERY; REPORTER; ORIGINS; BINDING; DRUGS; MODE;
D O I
10.1177/1087057116667255
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
One of the central questions in the characterization of enzyme inhibitors is determining the mode of inhibition (MOI). Classically, this is done with a number of low-throughput methods in which inhibition models are fitted to the data. The ability to rapidly characterize the MOI for inhibitors arising from high-throughput screening in which hundreds to thousands of primary inhibitors may need to be characterized would greatly help in lead selection efforts. Here we describe a novel method for determining the MOI of a compound without the need for curve fitting of the enzyme inhibition data. We provide experimental data to demonstrate the utility of this new high-throughput MOI classification method based on nonparametric analysis of the activity derived from a small matrix of substrate and inhibitor concentrations (e.g., from a 4(S) x 4(I) matrix). Lists of inhibitors from four different enzyme assays are studied, and the results are compared with the previously described IC50-shift method for MOI classification. The MOI results from this method are in good agreement with the known MOI and compare favorably with those from the IC50-shift method. In addition, we discuss some advantages and limitations of the method and provide recommendations for utilization of this MOI classification method.
引用
收藏
页码:1075 / 1089
页数:15
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