| Literature DB >> 28429463 |
Danyang Wang1, Shubo Du1, Amaury Cazenave-Gassiot2, Jingyan Ge3, Jun-Seok Lee4, Markus R Wenk2, Shao Q Yao1.
Abstract
The protein-lipid interaction is an essential metabolic process that mediates cellular signaling and functions. Existing strategies for large-scale mapping studies of the protein-lipid interaction fall short in their incompatibility with metabolic incorporation or inability to remove unwanted interferences from lipidated proteins. By incorporating an alkyne-containing choline head group and a diazirine-modified fatty acid simultaneously into choline-containing phospholipids synthesized from live mammalian cells, protein-phospholipid interactions have been successfully imaged in live cells. Subsequent in situ profiling of the modified Cho phospholipid-crosslinked proteins followed by quantitative proteomics allowed identification of several hundred putative phospholipid-interacting proteins, some of which were further validated.Entities:
Keywords: click chemistry; phosphatidylcholine; photo-crosslinking; protein-lipid interactions; quantitative proteomics
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Year: 2017 PMID: 28429463 DOI: 10.1002/anie.201702509
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336