Chemical proteomics: a powerful tool for exploring protein lipidation
File(s)BST20120283.pdf (1.76 MB)
Accepted version
Author(s)
Storck, EM
Serwa, RA
Tate, EW
Type
Journal Article
Abstract
The study of post-translational modifications such as protein lipidation is a non-trivial challenge of the post-genomic era. In recent years the field of chemical proteomics has greatly advanced our ability to identify and quantify protein lipidation. In the present review, we give a brief overview of the tools available to study protein acylation, prenylation and cholesterylation, and their application in the identification and quantification of protein lipidation in health and disease.
Date Issued
2013-02-01
Date Acceptance
2013-02-01
Citation
Biochemical Society Transactions, 2013, 41 (1), pp.56-61
ISSN
1470-8752
Publisher
Portland Press
Start Page
56
End Page
61
Journal / Book Title
Biochemical Society Transactions
Volume
41
Issue
1
Copyright Statement
The final version of record is available at http://www.biochemsoctrans.org/content/41/1/56
Subjects
Science & Technology
Life Sciences & Biomedicine
Biochemistry & Molecular Biology
BIOCHEMISTRY & MOLECULAR BIOLOGY
chemical proteomics
cholesterylation
fatty acylation
prenylation
stable isotope labelling by amino acids in cell culture (SILAC)
BIOORTHOGONAL LIGATION CHEMISTRY
N-MYRISTOYL TRANSFERASE
GERANYLGERANYLATED PROTEINS
MAMMALIAN-CELLS
CLICK CHEMISTRY
AMINO-ACIDS
IN-VIVO
PALMITOYLATION
INHIBITORS
IDENTIFICATION
Publication Status
Published