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- W2006175718 abstract "Characterization of small molecule (SM)–protein interaction is of high importance in biomedical research such as target identification and proteomic profiling. Photo-cross-linking is a powerful and straightforward strategy to covalently capture SM’s binding proteins. The DNA-based photoaffinity labeling method is able to capture SM’s protein targets with high specificity but suffers low cross-linking efficiency, which limits its utility for low abundance and low affinity proteins. After screening a variety of cross-linkers, by utilizing the multivalency effect, the cross-linking efficiency was improved by nearly 7-fold without compromising probe specificity. The generality and performance of multivalent photoaffinity probes have been validated with a variety of SM-protein pairs in the complexity of cell lysates." @default.
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- W2006175718 date "2014-06-03" @default.
- W2006175718 modified "2023-10-17" @default.
- W2006175718 title "Multivalent Photoaffinity Probe for Labeling Small Molecule Binding Proteins" @default.
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- W2006175718 doi "https://doi.org/10.1021/bc500195w" @default.
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