| Literature DB >> 28967196 |
Ke Cheng1, Jun-Seok Lee2, Piliang Hao3, Shao Q Yao4, Ke Ding1, Zhengqiu Li1.
Abstract
Target-identification phenotypic screening has been a powerful approach in drug discovery; however, it is hindered by difficulties in identifying the underlying cellular targets. To address this challenge, we have combined phenotypic screening of a fully functionalized small-molecule library with competitive affinity-based proteome profiling to map and functionally characterize the targets of screening hits. Using this approach, we identified ANXA2, PDIA3/4, FLAD1, and NOS2 as primary cellular targets of two bioactive molecules that inhibit cancer cell proliferation. We further demonstrated that a panel of probes can label and/or image annexin A2 (a cancer biomarker) from different cancer cell lines, thus providing opportunities for potential cancer diagnosis and therapy.Entities:
Keywords: affinity-based probes; cancer biomarkers; phenotypic screening; target identification; tetrazole
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Year: 2017 PMID: 28967196 DOI: 10.1002/anie.201709584
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336