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Updated: Aug 5, 2026

Simultaneous Affinity Enrichment of Two Post-Translational Modifications for Quantification and Site Localization
Published on: February 27, 2020
Characterization of Post-translational Modification in Metabolic Dysfunction-Associated Steatohepatitis: Acetylation,
Kuan Li1, Yundong Li1, Yuqing Zhang1
1Hepatobiliary surgery, the Affiliated Calmette Hospital of Kunming Medical University,the First Hospital of Kunming, No. 1228 Beijing Rd, Kunming, Yunnan 650000, PRC.
This study reveals widespread post-translational modification (PTM) changes in metabolic dysfunction-associated steatohepatitis (MASH). Key proteins like CMKLR1, CYP2E1, GLRX, and XRCC1 are identified as crucial targets for MASH intervention.
Area of Science:
- Biochemistry
- Molecular Biology
- Hepatology
Background:
- Metabolic dysfunction-associated steatohepatitis (MASH) involves complex pathological processes.
- Abnormalities in post-translational modifications (PTMs) are implicated in MASH progression.
Purpose of the Study:
- To characterize PTM features (acetylation, lactylation, phosphorylation) in MASH.
- To identify potential diagnostic markers and therapeutic targets for MASH.
Main Methods:
- Liquid chromatography-mass spectrometry (LC-MS) was used to analyze protein and modification profiles.
- Comparative analysis of liver tissues from normal and MASH patients.
- Identification of differentially expressed proteins (DEPs) and differentially modified proteins (DMPs).
Main Results:
- Acetylation and lactylation primarily occurred at lysine (K) residues, while phosphorylation occurred at serine (S) and threonine (T) residues.
- Proteomics identified numerous DEPs/DMPs regulating cytoskeleton, immunity, metabolism, and inflammatory pathways.
- CMKLR1, CYP2E1, GLRX, and XRCC1 were identified as key regulators with dysregulated expression in MASH.
Conclusions:
- This study systematically reveals global PTM dysregulation in MASH.
- Highlights CMKLR1, CYP2E1, GLRX, and XRCC1 as critical proteins and modification sites.
- Provides new perspectives for targeted interventions in MASH.
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