Time-resolved FRET reveals the structural mechanism of SERCA-PLB regulation

Biochemical and Biophysical Research Communications

Volumn 449, Issue 2, 2014, Pages 196-201

  Dong, Xiaoqiong ^a   Thomas, David D ^b  

^a University of Minnesota   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

Author keywords

FRET; Phospholamban; Phosphorylation; SERCA

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); CALCIUM; PHOSPHOLAMBAN;

ANIMAL TISSUE; ARTICLE; CONCENTRATION (PARAMETERS); CYTOPLASM; DISSOCIATION; ENZYME INHIBITION; FLUORESCENCE RESONANCE ENERGY TRANSFER; LIPID BILAYER; MOLECULAR MECHANICS; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN PHOSPHORYLATION; PROTEIN STRUCTURE; SARCOPLASMIC RETICULUM; TIME RESOLVED FLUORESCENCE RESONANCE ENERGY TRANSFER;

FRET; PHOSPHOLAMBAN; PHOSPHORYLATION; SERCA;

ANIMALS; CALCIUM-BINDING PROTEINS; FLUORESCENCE RESONANCE ENERGY TRANSFER; FLUORESCENT DYES; LIPID BILAYERS; MODELS, MOLECULAR; MULTIPROTEIN COMPLEXES; MUSCLE FIBERS, FAST-TWITCH; MYOCARDIUM; PHOSPHORYLATION; PROTEIN BINDING; PROTEIN INTERACTION DOMAINS AND MOTIFS; RABBITS; SARCOPLASMIC RETICULUM; SARCOPLASMIC RETICULUM CALCIUM-TRANSPORTING ATPASES;

EID: 84902082688     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2014.04.166     Document Type: Article

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