Development of Nuclear-Targeted Photoaffinity Probes with Cleavable Disulfide Bonds for Enhancing Selectivity in hPTM Interactome Profiling

Cell-penetrating, nuclear-targeted histone photoaffinity probes enable histone post-translational modification (hPTM) interactome profiling in native cells, yet noncleavable cell-penetrating peptides (e.g., cyclic polyarginine cell-penetrating peptide, cR10) induce interference due to their high positive charge. Herein, via facile synthesis, we developed novel nuclear-targeted histone photoaffinity probes with intracellularly cleavable cR10-disulfide linkages, targeting H3K4me3/H3K14la. In vitro labeling and proteomic assays demonstrated significantly improved binding selectivity for reader proteins and drastically reduced false-positive signals following cR10 cleavage.

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Publication Details

Journal
Organic Letters
Published
2026-03-16
DOI
https://doi.org/10.1021/acs.orglett.6c00381
Primary Topic
Click Chemistry and Applications
Type
article
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article

Development of Nuclear-Targeted Photoaffinity Probes with Cleavable Disulfide Bonds for Enhancing Selectivity in hPTM Interactome Profiling

Ding-Fei Yan, B. Wang, Yan Xu, Shihe Yang et al.
Organic Letters
Click Chemistry and Applications
article

Development of Nuclear-Targeted Photoaffinity Probes with Cleavable Disulfide Bonds for Enhancing Selectivity in hPTM Interactome Profiling

Ding-Fei Yan, B. Wang, Yan Xu, Shihe Yang, Fanghui Chen, Yu Wang, Yi-Ming Li, Ran Zhu
article en

Abstract

Cell-penetrating, nuclear-targeted histone photoaffinity probes enable histone post-translational modification (hPTM) interactome profiling in native cells, yet noncleavable cell-penetrating peptides (e.g., cyclic polyarginine cell-penetrating peptide, cR10) induce interference due to their high positive charge. Herein, via facile synthesis, we developed novel nuclear-targeted histone photoaffinity probes with intracellularly cleavable cR10-disulfide linkages, targeting H3K4me3/H3K14la. In vitro labeling and proteomic assays demonstrated significantly improved binding selectivity for reader proteins and drastically reduced false-positive signals following cR10 cleavage.

Organic LettersVol. 28(12)
Hefei University of Technology (CN), Protein Technologies (United Kingdom) (GB), Tsinghua University (CN)
Openalex Percentile: Top 19%
Click Chemistry and Applications
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