Endophilin BAR domain drives membrane curvature by two newly identified structure-based mechanisms

EMBO Journal

Volumn 25, Issue 12, 2006, Pages 2889-2897

  Masuda, Michitaka ^a   Takeda, Soichi ^a,b   Sone, Manami ^a   Ohki, Takashi ^a   Mori, Hidezo ^a   Kamioka, Yuji ^a   Mochizuki, Naoki ^a  

^a NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

^b RIKEN HARIMA INSTITUTE   (Japan)

Author keywords

BAR domain; Endophilin; Liposome; Membrane curvature; Membrane insertion

Indexed keywords

AMPHIPHYSIN; ENDOPHILIN; LIPOSOME;

AMINO TERMINAL SEQUENCE; ARTICLE; BILAYER MEMBRANE; BINDING AFFINITY; CRYSTAL STRUCTURE; GENE INSERTION; HUMAN; HUMAN CELL; HYDROPHOBICITY; MEMBRANE BINDING; NERVE SPROUTING; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FAMILY; PROTEIN STRUCTURE; STRUCTURE ANALYSIS;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SEQUENCE; ANIMALS; CELL MEMBRANE; CELLS, CULTURED; CERCOPITHECUS AETHIOPS; CHO CELLS; COS CELLS; CRICETINAE; FLUORESCENCE; FLUORESCENCE RESONANCE ENERGY TRANSFER; HUMANS; HYDROPHOBICITY; LIPOSOMES; MICE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; NIH 3T3 CELLS; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; TRYPTOPHAN;

EID: 33745559393     PISSN: 02614189     EISSN: 14602075     Source Type: Journal    
DOI: 10.1038/sj.emboj.7601176     Document Type: Article

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