Positions of polar amino acids alter interactions between transmembrane segments and detergents

Biochemistry

Volumn 50, Issue 19, 2011, Pages 3928-3935

  Tulumello, David V ^a   Deber, Charles M ^a,b  

^a HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BI-LAYER; BLUE SHIFT; C-TERMINUS; DISEASE STATE; HYDROPHOBIC AMINO ACIDS; HYDROPHOBIC REGIONS; IN-VITRO; MEMBRANE BILAYERS; MEMBRANE PROTEINS; NON-POLAR; POINT MUTATIONS; POLAR AMINO ACIDS; POLAR RESIDUES; PROTEIN STRUCTURES; PROTEIN-LIPID INTERACTIONS; REFOLDING; SODIUM DODECYL SULFATE-POLYACRYLAMIDE GEL ELECTROPHORESIS; TRANSMEMBRANE SEGMENTS; TRANSMEMBRANES; TRP-FLUORESCENCE; TRYPTOPHAN FLUORESCENCE;

AMINO ACIDS; BIOLOGICAL MEMBRANES; CIRCULAR DICHROISM SPECTROSCOPY; COMPLEXATION; CYTOLOGY; DICHROISM; ELECTROPHORESIS; FLUORESCENCE; HYDROPHOBICITY; PEPTIDES; PHOSPHOLIPIDS; SODIUM; SODIUM SULFATE; SOLVATION;

SOAPS (DETERGENTS);

ALPHA HELICAL TRANSMEMBRANE SEGMENT; AMINO ACID; ASPARAGINE; DODECYL SULFATE SODIUM; MEMBRANE PROTEIN; PHOSPHOLIPID; TRYPTOPHAN; UNCLASSIFIED DRUG;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CIRCULAR DICHROISM; FLUORESCENCE; POINT MUTATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN FOLDING; SOLVATION;

ALANINE; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ASPARAGINE; DETERGENTS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; PEPTIDE FRAGMENTS; PROTEIN FOLDING; PROTEIN STRUCTURE, SECONDARY; SODIUM DODECYL SULFATE; TRYPTOPHAN;

EID: 79955864550     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi200238g     Document Type: Article

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