Defining dynamic protein interactions using SILAC-based quantitative mass spectrometry

Methods in Molecular Biology

Volumn 1188, Issue , 2014, Pages 191-205

  Wang, Xiaorong ^a   Huang, Lan ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

AP MS; Dynamic interactors; HB tag; MAP SILAC; PAM SILAC; Proteasome interacting proteins; Protein protein interaction; Quantitative mass spectrometry; Stable interactors; Tc PAM SILAC

Indexed keywords

ARTICLE; CELL LABELING; CELL LYSATE; CONTROLLED STUDY; HUMAN; HUMAN CELL; INCUBATION TIME; MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN PROTEIN INTERACTION; PROTEIN PURIFICATION; STABLE ISOTOPE LABELING OF AMINO ACIDS IN CELL CULTURE; CHEMISTRY; GENETIC TRANSFECTION; GENETICS; HEK293 CELL LINE; ISOLATION AND PURIFICATION; ISOTOPE LABELING; LIQUID CHROMATOGRAPHY; METABOLISM; PROCEDURES; PROTEIN ANALYSIS; PROTEIN DEGRADATION; TANDEM MASS SPECTROMETRY; TIME;

ADRM1 PROTEIN, HUMAN; AMINO ACID; MEMBRANE PROTEIN; PROTEIN;

AMINO ACIDS; CHROMATOGRAPHY, LIQUID; HEK293 CELLS; HUMANS; ISOTOPE LABELING; MASS SPECTROMETRY; MEMBRANE GLYCOPROTEINS; PROTEIN INTERACTION MAPPING; PROTEINS; PROTEOLYSIS; TANDEM MASS SPECTROMETRY; TIME FACTORS; TRANSFECTION;

EID: 84925884234     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4939-1142-4_14     Document Type: Article

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