# Chemical Proteomics Identifies Ketogenesis‐Mediated Cysteine Modifications Regulating Redox Function

## TL;DR

This study shows that ketone bodies can modify cysteine in proteins, affecting redox function, and identifies a new type of modification called cysteine crotonation.

## Contribution

The study introduces a new chemical probe and identifies cysteine crotonation as a novel ketogenesis-mediated modification.

## Key findings

- Acetoacetate induces cysteine modifications, including crotonation, in mammalian cells.
- Cysteine crotonation at PRDX3 C229 impairs dimerization and redox activity.
- BDH1 and ECHS1 are key enzymes involved in cysteine crotonation formation.

## Abstract

All the studies of ketogenesis‐dependent post‐translational modifications (PTMs), notably those mediated by ketone bodies, β‐hydroxybutyrate (Bhb) and acetoacetate (Acac), have focused on lysine acylations. However, given the chemically diverse and reactive nature of metabolites generated, it remains unclear whether non‐lysine modifications can also happen. Here, we develop an acetoacetate‐alkyne (Acac‐alkyne) chemical probe that enables efficient metabolic labeling, robust fluorescent visualization, and site‐specific identification of Acac‐modified proteins. By combining chemical proteomics with open‐search strategy, we showed that Acac induces previously uncharacterized cysteine modifications in mammalian cells. Notably, cysteine crotonation (Ccr) is validated by employing both probe‐based and standard peptide‐based co‐elution assays. Metabolic pathway tracing further identifies BDH1 and ECHS1 as key enzymes that generate Ccr formation. We further demonstrate that Ccr at PRDX3 C229 site impairs dimerization and redox activity, linking this newly discovered modification to the regulation of cellular reactive oxygen species. Together, these findings establish ketone metabolism as a novel source of cysteine modifications and provide an alternative mechanistic pathway to explain the profound biological effects of ketone bodies.

Herein, we report ketone body induce cysteine modifications beyond lysine acylation, as revealed by integrating chemical proteomics with open‐search methods. Among the modifications, cysteine crotonation (Ccr) was chemically validated by endogenous peptide‐based co‐elution assays. Metabolic tracing identifies BDH1 and ECHS1 as key Ccr‐generating enzymes. Functional studies showed that Ccr at C229 of PRDX3 impairs dimerization and redox function.