| Literature DB >> 16751338 |
Yulong Hong1, Brian L Webb, Sadashiva Pai, Ann Ferrie, Jinlin Peng, Fang Lai, Joydeep Lahiri, Gloria Biddlecome, Brian Rasnow, Michael Johnson, Hosung Min, Ye Fang, John Salon.
Abstract
Conventional assay methods for discovering and profiling drug-target interactions are typically developed on a target-by-target basis and hence can be cumbersome to enable and orchestrate. Herein the authors report a solid-state ligand-binding assay that operates in a multiplexed mode to report compound activity against a micorarray-configured panel of G-protein-coupled receptor (GPCR) targets. The pharmacological fidelity of the system is high, and its miniaturized "plug-and-play" format provides improved efficiency both in terms of execution time and reagent consumption. Taken together, these features make the system ideally suited to explore the structure-activity relationship of compounds across a broad region of target class space.Mesh:
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Year: 2006 PMID: 16751338 DOI: 10.1177/1087057106287139
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571