Fluorescence Resonance Energy Transfer (FRET) indicates that association with the type I ryanodine receptor (RyR1) causes reorientation of multiple cytoplasmic domains of the dihydropyridine receptor (DHPR) α1s subunit

Journal of Biological Chemistry

Volumn 287, Issue 49, 2012, Pages 41560-41568

  Polster, Alexander ^a,b   Ohrtman, Joshua D ^b   Beam, Kurt G ^b   Papadopoulos, Symeon ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

^b UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL MEMBRANES; CELL PROLIFERATION; ENERGY TRANSFER; INSECTICIDES; MUSCLE; PROTEINS; PYRIDINE;

CYTOPLASMIC DOMAINS; DIHYDROPYRIDINE RECEPTORS; FLUORESCENCE RESONANCE ENERGY TRANSFER; FLUORESCENT PROTEIN; RYANODINE RECEPTORS; SARCOPLASMIC RETICULUM; SPATIAL RELATIONSHIPS; TUBULAR MEMBRANES;

FORSTER RESONANCE ENERGY TRANSFER;

1,4 DIHYDROPYRIDINE RECEPTOR; DIHYDROPYRIDINE RECEPTOR ALPHA SUBUNIT; RYANODINE RECEPTOR 1; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BINDING AFFINITY; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CELL SURFACE; CONTROLLED STUDY; CYTOPLASM; FLUORESCENCE RESONANCE ENERGY TRANSFER; MOLECULAR DYNAMICS; MOUSE; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN TARGETING; SIGNAL TRANSDUCTION;

EID: 84870387573     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.404194     Document Type: Article

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