The endophilin N-BAR domain perturbs the structure of lipid bilayers

Biochemistry

Volumn 49, Issue 27, 2010, Pages 5766-5771

  Suresh, Swetha ^a   Edwardson, J Michael ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BENDING MECHANISM; BI-LAYER; BILAYER SHEETS; CLATHRIN-MEDIATED ENDOCYTOSIS; ENDOPHILIN; LOW CONCENTRATIONS; MEMBRANE BINDING; NERVE TERMINALS; PHYSIOLOGICAL CONDITION; PLANAR BILAYERS; PLANAR SUPPORTED LIPID BILAYERS; SYNAPTIC TRANSMISSION;

ATOMIC FORCE MICROSCOPY; HYDROPHOBICITY; MOLECULAR BIOLOGY;

LIPID BILAYERS;

ALANINE; ASPARTIC ACID; CLATHRIN; ENDOPHILIN; ENDOPHILIN A; LIPID; TRYPTOPHAN; UNCLASSIFIED DRUG; 2 ACYLGLYCEROPHOSPHATE ACYLTRANSFERASE; 2-ACYLGLYCEROPHOSPHATE ACYLTRANSFERASE; ACYLTRANSFERASE;

ARTICLE; CONTROLLED STUDY; HYDROPHOBICITY; LIPID BILAYER; MEMBRANE BINDING; MOUSE; NERVE ENDING; NONHUMAN; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN DOMAIN; PROTEIN LIPID INTERACTION; SYNAPTIC TRANSMISSION; ATOMIC FORCE MICROSCOPY; CHEMISTRY; ENDOCYTOSIS; METABOLISM; SRC HOMOLOGY DOMAIN;

ACYLTRANSFERASES; ENDOCYTOSIS; HYDROPHOBICITY; LIPID BILAYERS; MICROSCOPY, ATOMIC FORCE; SRC HOMOLOGY DOMAINS;

EID: 77954700056     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi100760e     Document Type: Article

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