Literature DB >> 19235135

Analysis of protein acylation.

Ruth Zeidman1, Caroline S Jackson, Anthony I Magee.   

Abstract

Proteins can be acylated with a variety of fatty acids attached by different covalent bonds, influencing, among other things, their function and intracellular localization. This unit describes methods to analyze protein acylation, both levels of acylation and also the identification of the fatty acid and the type of bond present in the protein of interest. Protocols are provided for metabolic labeling of proteins with tritiated fatty acids, for exploitation of the differential sensitivity to cleavage of different types of bonds, in order to distinguish between them, and for thin-layer chromatography to separate and identify the fatty acids associated with proteins.

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Year:  2009        PMID: 19235135     DOI: 10.1002/0471140864.ps1402s55

Source DB:  PubMed          Journal:  Curr Protoc Protein Sci        ISSN: 1934-3655


  1 in total

1.  Unconventional myristoylation of large-conductance Ca²⁺-activated K⁺ channel (Slo1) via serine/threonine residues regulates channel surface expression.

Authors:  Abderrahmane Alioua; Min Li; Yong Wu; Enrico Stefani; Ligia Toro
Journal:  Proc Natl Acad Sci U S A       Date:  2011-06-13       Impact factor: 11.205

  1 in total

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