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

Author:

Auld Douglas S.1,Jimenez Marta1,Yue Kimberley1,Busby Scott1,Chen Yu-Chi12,Bowes Scott1,Wendel Greg1,Smith Thomas1,Zhang Ji-Hu1

Affiliation:

1. Novartis Institutes for Biomedical Research, Center for Proteomic Chemistry, Cambridge, MA, USA

2. National Center for Advancing Translational Sciences, Bethesda, MD, USA

Abstract

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 4S × 4I 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.

Publisher

Elsevier BV

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. High-Throughput Mechanism of Inhibition;SLAS DISCOVERY: Advancing the Science of Drug Discovery;2021-01-22

2. Enzyme–Inhibitor Interactions and a Simple, Rapid Method for Determining Inhibition Modality;SLAS DISCOVERY: Advancing the Science of Drug Discovery;2019-02-27

3. ADMETopt: A Web Server for ADMET Optimization in Drug Design via Scaffold Hopping;Journal of Chemical Information and Modeling;2018-09-25

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