Issue 1, 2021

A peptidic inhibitor for PD-1 palmitoylation targets its expression and functions

Abstract

Programmed cell death protein 1 (PD-1) is a crucial anticancer target, but the relatively low response rate and acquired resistance to existing antibody drugs highlight an urgent need to develop alternative targeting strategies. Here, we report the palmitoylation of PD-1, discover the main DHHC enzyme for this modification, reveal the mechanism of its effect on PD-1 protein stability, and rationally develop a peptide for targeting PD-1 expression. Palmitoylation promoted the trafficking of PD-1 to the recycling endosome, thus preventing its lysosome-dependent degradation. Palmitoylation of PD-1, but not of PD-L1, promoted mTOR signaling and tumor cell proliferation, and targeting palmitoylation displayed significant anti-tumor effects in a three-dimensional culture system. A peptide was designed to competitively inhibit PD-1 palmitoylation and expression, opening a new route for developing PD-1 inhibitors and combinatorial cancer immunotherapy.

Graphical abstract: A peptidic inhibitor for PD-1 palmitoylation targets its expression and functions

Supplementary files

Article information

Article type
Paper
Submitted
25 ago 2020
Accepted
05 out 2020
First published
03 nov 2020
This article is Open Access
Creative Commons BY-NC license

RSC Chem. Biol., 2021,2, 192-205

A peptidic inhibitor for PD-1 palmitoylation targets its expression and functions

H. Yao, C. Li, F. He, T. Song, J. Brosseau, H. Wang, H. Lu, C. Fang, H. Shi, J. Lan, J. Fang and J. Xu, RSC Chem. Biol., 2021, 2, 192 DOI: 10.1039/D0CB00157K

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