Selective proteomic proximity labeling assay using tyramide (SPPLAT): A quantitative method for the proteomic analysis of localized membrane-bound protein clusters

Current Protocols in Protein Science

Volumn 2017, Issue , 2017, Pages

  Rees, Johanna Susan ^a   Li, Xue Wen ^b   Perrett, Sarah ^b   Lilley, Kathryn Susan ^a   Jackson, Antony Philip ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b INSTITUTE OF BIOPHYSICS   (China)

Author keywords

Protein microenvironments; Proteomics; Proximity; Quantitative; SPPLAT

Indexed keywords

AMINO ACID; ANTIBODY; BIOTIN; BIOTINYLTYRAMIDE; HORSERADISH PEROXIDASE; MEMBRANE PROTEIN; PEPTIDE; TYRAMINE;

ANALOGS AND DERIVATIVES; ANIMAL; CELL LINE; CELL MEMBRANE; CHEMISTRY; HUMAN; IMMUNOLOGY; ISOTOPE LABELING; LIQUID CHROMATOGRAPHY; PROCEDURES; PROTEOMICS; TANDEM MASS SPECTROMETRY;

AMINO ACIDS; ANIMALS; ANTIBODIES; BIOTIN; CELL LINE; CELL MEMBRANE; CHROMATOGRAPHY, LIQUID; HORSERADISH PEROXIDASE; HUMANS; ISOTOPE LABELING; MEMBRANE PROTEINS; PEPTIDES; PROTEOMICS; TANDEM MASS SPECTROMETRY; TYRAMINE;

EID: 85021856713     PISSN: 19343655     EISSN: 19343663     Source Type: Journal    
DOI: 10.1002/cpps.27     Document Type: Article

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