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Bridging oxidative post-translational modifications to biological meaning
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DOI：10.1016/j.tcb.2026.05.004.png)
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Abstract
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Redox proteomics has revealed thousands of oxidative post-translational modifications across the proteome. The functional consequences of most oxidative post-translational modifications remain unknown. Fold change-based ranking enriches for highly reactive cysteines but can miss low-stoichiometry allosteric redox switches. Functional genomic screens provide an orthogonal approach to deconvolute the importance of redox-active sites identified in proteomic analysis.
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