How curvature-generating proteins build scaffolds on membrane nanotubes

Proceedings of the National Academy of Sciences of the United States of America

Volumn 113, Issue 40, 2016, Pages 11226-11231

  Simunovic, Mijo ^a,b,c,d,i   Evergren, Emma ^e,j   Golushko, Ivan ^f   Prévost, Coline ^a,k   Renard, Henri François ^g,l   Johannes, Ludger ^g   McMahon, Harvey T ^e   Lorman, Vladimir ^f   Voth, Gregory A ^b,c,d   Bassereau, Patricia ^a,h  

^a INSTITUT CURIE   (France)

^b UNIVERSITY OF CHICAGO   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d UNIVERSITY OF CHICAGO   (United States)

^e MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

^f UNIVERSITÉ MONTPELLIER 2   (France)

^g CNRS UMR3666   (France)

^h SORBONNE UNIVERSITÉ   (France)

ⁱ ROCKEFELLER UNIVERSITY   (United States)

^j QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^k HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^l UNIVERSITÉ CATHOLIQUE DE LOUVAIN   (Belgium)

more..

Author keywords

BAR proteins; Endocytosis; Membrane curvature; Protein scaffold; Self assembly

Indexed keywords

ADAPTOR PROTEIN; AMPHIPHYSIN; BETA2 CENTAURIN; ENDOPHILIN; ENDOPHILIN A2; EPSIN; EPSIN 1; MEMBRANE PROTEIN; MOLECULAR SCAFFOLD; NANOTUBE; PROTEIN BIN; PROTEIN CENTAURIN; PROTEIN RVS; UNCLASSIFIED DRUG; LIPID; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ARTICLE; BINDING SITE; FLUORESCENCE MICROSCOPY; LIPID MEMBRANE; MATHEMATICAL MODEL; MICROSCOPY; MOLECULAR DYNAMICS; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN BINDING; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; SIMULATION; CALIBRATION; CELL MEMBRANE; CHEMISTRY; COMPUTER SIMULATION; FLUORESCENCE; METABOLISM; PROTEIN SECONDARY STRUCTURE; STRUCTURAL HOMOLOGY; SURFACE PROPERTY; X RAY;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; BINDING SITES; CALIBRATION; CELL MEMBRANE; COMPUTER SIMULATION; FLUORESCENCE; LIPIDS; MEMBRANE PROTEINS; MOLECULAR DYNAMICS SIMULATION; NANOTUBES; PROTEIN DOMAINS; PROTEIN STRUCTURE, SECONDARY; STRUCTURAL HOMOLOGY, PROTEIN; SURFACE PROPERTIES; X-RAYS;

EID: 84989935188     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1606943113     Document Type: Article

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