Liposome Binding Assay to Characterize the Structure and Function of Cavin Proteins.
Caveolae
Cavin
Coat protein
Liposome binding
Liposome flotation
Proteoliposome
Reconstitution
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
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