Altering hydrophobic sequence lengths shows that hydrophobic mismatch controls affinity for ordered lipid domains (rafts) in the multitransmembrane strand protein perfringolysin O

Journal of Biological Chemistry

Volumn 288, Issue 2, 2013, Pages 1340-1352

  Lin, Qingqing ^a   London, Erwin ^a  

^a STONY BROOK UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BI-LAYER; DISORDERED DOMAINS; GIANT VESICLES; HYDROPHOBIC MISMATCH; HYDROPHOBIC SEQUENCES; MEMBRANE INSERTION; MULTIMERIC; ORDERED DOMAINS; ORDERED LIPID DOMAINS; PHOSPHATIDYLCHOLINE; PORE FORMATION; PROTEIN AFFINITY; SPHINGOMYELIN; TRANSMEMBRANES; WIDTH CONTROL; WILD TYPES;

CHOLESTEROL; HYDROPHOBICITY; PHOSPHOLIPIDS;

PROTEINS;

CHOLESTEROL; CLOSTRIDIUM PERFRINGENS TOXIN; MEMBRANE PROTEIN; PHOSPHATIDYLCHOLINE; SPHINGOMYELIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BILAYER MEMBRANE; BINDING AFFINITY; CONTROLLED STUDY; FLUORESCENCE RESONANCE ENERGY TRANSFER; HYDROPHOBIC MISMATCH; LIPID RAFT; MEMBRANE VESICLE; MICROSCOPY; MOLECULAR BIOLOGY; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DOMAIN;

BACTERIAL TOXINS; BASE SEQUENCE; CENTRIFUGATION; DNA PRIMERS; FLUORESCENCE RESONANCE ENERGY TRANSFER; HEMOLYSIN PROTEINS; LIPID BILAYERS; LIPIDS; MUTATION; SPECTROMETRY, FLUORESCENCE;

EID: 84872325526     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.415596     Document Type: Article

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