Mass-tag labeling reveals site-specific and endogenous levels of protein S-fatty acylation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 113, Issue 16, 2016, Pages 4302-4307

  Percher, Avital ^a   Ramakrishnan, Srinivasan ^a   Thinon, Emmanuelle ^a   Yuan, Xiaoqiu ^a   Yount, Jacob S ^a,b   Hang, Howard C ^a  

^a ROCKEFELLER UNIVERSITY   (United States)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

Fatty acylation; IFITM3; Influenza virus; Palmitoylation; Pegylation

Indexed keywords

CYSTEINE; INTERFERON; PROTEIN S; FATTY ACID; MEMBRANE PROTEIN;

3T3 CELL LINE; ACYLATION; ANTIVIRAL ACTIVITY; ARTICLE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; ENDOSOME; FATTY ACYLATION; FLOW CYTOMETRY; HUMAN; IMMUNOFLUORESCENCE; INFLUENZA VIRUS; PALMITOYLATION; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN PROCESSING; QUANTITATIVE STUDY; WESTERN BLOTTING; ANIMAL; MASS SPECTROMETRY; METABOLISM; MOUSE; PHYSIOLOGY; PROCEDURES; STAINING;

ACYLATION; ANIMALS; CYSTEINE; FATTY ACIDS; MASS SPECTROMETRY; MEMBRANE PROTEINS; MICE; PROTEIN PROCESSING, POST-TRANSLATIONAL; STAINING AND LABELING;

EID: 84964324810     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1602244113     Document Type: Article

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