High-Throughput Dose-Response Measurement Using a Label-Free Microarray-in-Microplate Assay Platform

被引:10
|
作者
Landry, J. P. [1 ]
Malovichko, G. [1 ]
Zhu, X. D. [1 ]
机构
[1] Univ Calif Davis, Dept Phys, Davis, CA 95616 USA
关键词
SMALL MOLECULES; TARGETS; CANCER; LIBRARIES;
D O I
10.1021/acs.analchem.5b00720
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Microarray-based binding assays facilitate the discovery of protein ligands from large collections of small molecules. Hundreds of ligands can be identified, yet only a small portion of them have interfering effects (competitive or noncompetitive) on a specific protein-receptor binding reaction. Further efficient screening of ligands for those with specific modifying effect is needed in order to take the full advantage of throughputs of microarray-based assays for drug discovery. We report a label-free microarray-in-microplate assay platform for simultaneous acquisition of at least 32 dose-response curves in a single experiment, each curve having 12 concentration points. When combined with ligand discovery, this makes the microarray-based platform a true high-throughout means of finding inhibitors to specific protein-receptor reactions starting from a large collection of small-molecule libraries.
引用
收藏
页码:5640 / 5648
页数:9
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