Identification of GABAc receptor protein homeostasis network components from three tandem mass spectrometry proteomics approaches

Journal of Proteome Research

Volumn 12, Issue 12, 2013, Pages 5570-5586

  Wang, Ya Juan ^a,b   Han, Dong Yun ^a   Tabib, Tracy ^c   Yates III, John R ^b   Mu, Ting Wei ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

^c AMERICAN UNIVERSITY   (United States)

Author keywords

degradation; folding; GABAC receptor; heat shock response; interactome; proteostasis; tandem mass spectrometry; trafficking; unfolded protein response

Indexed keywords

4 AMINOBUTYRIC ACID C RECEPTOR; CALNEXIN; HEAT SHOCK TRANSCRIPTION FACTOR 1; LECTIN; PROTEIN; PROTEIN LMAN1; UNCLASSIFIED DRUG; X BOX BINDING PROTEIN 1; 4 AMINOBUTYRIC ACID RECEPTOR; DNA BINDING PROTEIN; EYE PROTEIN; GABA-C RECEPTOR; HEAT SHOCK TRANSCRIPTION FACTOR; LMAN1 PROTEIN, HUMAN; MANNOSE BINDING LECTIN; MEMBRANE PROTEIN; PROTEIN BINDING; PROTEIN SUBUNIT; REGULATORY FACTOR X TRANSCRIPTION FACTORS; TRANSCRIPTION FACTOR;

ARTICLE; CELL STRAIN HEK293; CONTROLLED STUDY; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; IMMUNOPRECIPITATION; MULTIDIMENSIONAL PROTEIN IDENTIFICATION TECHNOLOGY; PRIORITY JOURNAL; PROCEDURES; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN HOMEOSTASIS; PROTEOMICS; TANDEM MASS SPECTROMETRY; ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY; UNFOLDED PROTEIN RESPONSE; WESTERN BLOTTING; BINDING SITE; CHEMISTRY; ENDOPLASMIC RETICULUM; GENE EXPRESSION REGULATION; GENETICS; HEK293 CELL LINE; HOMEOSTASIS; METABOLISM; PROTEIN MULTIMERIZATION; PROTEIN SUBUNIT;

BINDING SITES; CALNEXIN; DNA-BINDING PROTEINS; ENDOPLASMIC RETICULUM; EYE PROTEINS; GENE EXPRESSION REGULATION; HEK293 CELLS; HOMEOSTASIS; HUMANS; MANNOSE-BINDING LECTINS; MEMBRANE PROTEINS; PROTEIN BINDING; PROTEIN FOLDING; PROTEIN MULTIMERIZATION; PROTEIN SUBUNITS; PROTEOMICS; RECEPTORS, GABA; TANDEM MASS SPECTROMETRY; TRANSCRIPTION FACTORS; UNFOLDED PROTEIN RESPONSE;

EID: 84890033475     PISSN: 15353893     EISSN: 15353907     Source Type: Journal    
DOI: 10.1021/pr400535z     Document Type: Article

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