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Anal Chem ; 87(11): 5640-8, 2015 Jun 02.
Article in English | MEDLINE | ID: mdl-25921700

ABSTRACT

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.


Subject(s)
Biological Assay/methods , Dose-Response Relationship, Drug , Microarray Analysis/instrumentation , Immobilized Proteins , Ligands , Staining and Labeling
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