Probing small-molecule microarrays with tagged proteins in cell lysates.
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Abstract | The technique of small-molecule microarray (SMM) screening is based on the ability of small molecules to bind to various soluble proteins. This type of interaction is easily detected by the presence of a fluorescence signal produced by labeled antibodies that specifically recognize a unique sequence (tag) present on the target protein. The fluorescent signal intensity values are determined based on signal-to-noise ratios (SNRs). SMM screening is a high-throughput, unbiased method that can rapidly identify novel direct ligands for various protein targets. This binding-based assay format is generally applicable to most proteins, but it is especially useful for protein targets that do not possess an enzymatic activity. SMMs enable screening a protein in a purified form or in the context of a cellular lysate, likely providing a more physiologically relevant screening environment. |
Year of Publication | 2014
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Journal | Curr Protoc Chem Biol
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Volume | 6
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Issue | 4
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Pages | 209-20
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Date Published | 2014 Dec 01
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ISSN | 2160-4762
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DOI | 10.1002/9780470559277.ch140101
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PubMed ID | 25445177
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PubMed Central ID | PMC4266996
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Grant list | R01 CA160860 / CA / NCI NIH HHS / United States
CA160860 / CA / NCI NIH HHS / United States
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