Literature DB >> 30317507

Determination of Sec18-Lipid Interactions by Liposome-Binding Assay.

Matthew L Starr1, Rutilio Fratti2.   

Abstract

Protein-lipid binding interactions play a key role in the regulation of peripheral membrane protein function. Liposome-binding assays are a simple and affordable means of screening for specific protein-lipid interactions. Liposomes are prepared by mixing phospholipid combinations of interest before drying and rehydration. Sonication of the lipid mixture produces small unilamellar vesicles (SUVs) which are incubated with a protein of interest to allow for any binding to occur. Liposomes and liposome-protein complexes are floated on a sucrose gradient by centrifugation to separate them from unbound protein. Bound protein levels are easily determined by SDS-PAGE and Western blotting. This approach provides a reliable means of assaying novel protein-lipid interactions in vitro. Here we use liposome floatation to show the binding of the SNARE-activating protein Sec18 (mammalian NSF) to phosphatidic acid.

Entities:  

Keywords:  Liposome; Membrane fusion; Membrane trafficking; NSF; Phosphatidic acid; Phospholipids; SNARE; Sec18

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Year:  2019        PMID: 30317507     DOI: 10.1007/978-1-4939-8760-3_13

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  StaR-related lipid transfer-like domain-containing protein CLDP43 affects cardiolipin synthesis and mitochondrial function in Trypanosoma brucei.

Authors:  Alessio Loffreda; Michael Schlame; Peter Bütikofer
Journal:  PLoS One       Date:  2022-04-22       Impact factor: 3.752

  1 in total

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