Large-scale profiling of protein palmitoylation in mammalian cells

被引:0
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作者
Martin B.R. [1 ]
Cravatt B.F. [1 ]
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[1] The Skaggs Institute of Chemical Biology, Department of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037
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D O I
10.1038/nmeth.1293
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摘要
S-palmitoylation is a pervasive post-translational modification required for the trafficking, compartmentalization and membrane tethering of many proteins. We demonstrate that the commercially available compound 17-octadecynoic acid (17-ODYA) can serve as a bioorthogonal, click chemistry probe for in situ labeling, identification and verification of palmitoylated proteins in human cells. We identified ∼125 predicted palmitoylated proteins, including G proteins, receptors and a family of uncharacterized hydrolases whose plasma membrane localization depends on palmitoylation.
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页码:135 / 138
页数:3
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