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

Curr Opin Chem Biol

Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, NY 10065, United States; Departments of Immunology and Microbiology and Chemistry, Scripps Research, La Jolla, CA 92037, United States. Electronic address:

Published: December 2021

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671186PMC
http://dx.doi.org/10.1016/j.cbpa.2021.06.004DOI Listing

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