Liposome Binding Assay to Characterize the Structure and Function of Cavin Proteins.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2020
Historique:
entrez: 18 6 2020
pubmed: 18 6 2020
medline: 1 4 2021
Statut: ppublish

Résumé

Protein-protein and protein-lipid interactions play important roles in the assembly of protein coats that regulate membrane organization, signaling, and trafficking in eukaryotic cells. Caveolae are plasma membrane invaginations that are formed by a protein coat consisting of caveolin and cavin protein complexes. The biochemical and structural principles of membrane binding by coat components can be studied through in vitro reconstitution of purified proteins and lipid vesicles. In this chapter, we describe a method to isolate peripheral cavin coat complexes and to subsequently bind purified cavin to chemically defined liposomes. The cavin proteoliposomes can be further analyzed to gain insights into lipid binding specificity, membrane-remodeling properties, and structural characteristics of the cavin family members.

Identifiants

pubmed: 32548825
doi: 10.1007/978-1-0716-0732-9_12
doi:

Substances chimiques

CAVIN1 protein, human 0
Liposomes 0
Membrane Proteins 0
RNA-Binding Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

129-136

Auteurs

Miriam Stoeber (M)

Department of Cell Physiology and Metabolism, University of Geneva, Geneva, Switzerland. miriam.stoeber@unige.ch.

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Classifications MeSH