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Updated: Oct 26, 2025

Detection of Protein S-Acylation using Acyl-Resin Assisted Capture
Published on: April 10, 2020
Chemical approaches for investigating site-specific protein S-fatty acylation
Emma H Garst1, Tandrila Das1, Howard C Hang2
1Laboratory of Chemical Biology and Microbial Pathogenesis, The Rockefeller University, New York, NY 10065, United States; Tri-Institutional Ph.D. Program in Chemical Biology, New York, NY 10065, United States.
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.
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