| Literature DB >> 25803566 |
Aneika C Leney, Reza Rezaei Darestani, Jun Li, Sanaz Nikjah, Elena N Kitova, Chunxia Zou, Christopher W Cairo, Zi Jian Xiong1, Gilbert G Privé1,2, John S Klassen.
Abstract
Protein interactions with glycolipids are implicated in diverse cellular processes. However, the study of protein-glycolipid complexes remains a significant experimental challenge. Here, we describe a powerful new assay that combines electrospray ionization mass spectrometry (ESI-MS) and picodiscs, which are composed of human sphingolipid activator protein saposin A and a small number of phospholipids, to display glycolipids in a lipid environment for protein-glycolipid interaction studies in aqueous solution. Time-resolved measurements of enzyme catalyzed hydrolysis of glycolipid substrates and the detection of low, moderate, and high affinity protein-glycolipid interactions serve to demonstrate the reliability and versatility of the assay.Entities:
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Year: 2015 PMID: 25803566 DOI: 10.1021/acs.analchem.5b00170
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986