Literature DB >> 34333222

Chemical approaches for investigating site-specific protein S-fatty acylation.

Emma H Garst1, Tandrila Das1, Howard C Hang2.   

Abstract

Protein S-fatty acylation or S-palmitoylation is a reversible and regulated lipid post-translational modification (PTM) in eukaryotes. Loss-of-function mutagenesis studies have suggested important roles for protein S-fatty acylation in many fundamental biological pathways in development, neurobiology, and immunity that are also associated with human diseases. However, the hydrophobicity and reversibility of this PTM have made site-specific gain-of-function studies more challenging to investigate. In this review, we summarize recent chemical biology approaches and methods that have enabled site-specific gain-of-function studies of protein S-fatty acylation and the investigation of the mechanisms and significance of this PTM in eukaryotic biology.
Copyright © 2021 Elsevier Ltd. All rights reserved.

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Year:  2021        PMID: 34333222      PMCID: PMC8671186          DOI: 10.1016/j.cbpa.2021.06.004

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  57 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-10       Impact factor: 11.205

8.  Protein chemical synthesis by serine and threonine ligation.

Authors:  Yinfeng Zhang; Ci Xu; Hiu Yung Lam; Chi Lung Lee; Xuechen Li
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-08       Impact factor: 11.205

9.  Peptide Ligations by Using Aryloxycarbonyl-o-methylaminoanilides: Chemical Synthesis of Palmitoylated Sonic Hedgehog.

Authors:  Judith Palà-Pujadas; Fernando Albericio; Juan B Blanco-Canosa
Journal:  Angew Chem Int Ed Engl       Date:  2018-11-08       Impact factor: 15.336

10.  Bioorthogonal reactions for labeling proteins.

Authors:  Kathrin Lang; Jason W Chin
Journal:  ACS Chem Biol       Date:  2014-01-17       Impact factor: 5.100

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