Author

R.-X. Sun

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

B. Qin· 1 shared H.-J. Zhu· 1 shared J. Ji· 1 shared J.-N. Wang· 1 shared J.-X. Zhao· 1 shared M.-Q. Dong· 1 shared M.-Q. Zuo· 1 shared Q.-D. Shen· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCell Biology

B. Qin

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Lactylation-driven FTO-mediated m6A modification of CDK2 aggravates diabetic microvascular anomalies

X. Chen, R.-X. Sun, J.-N. Wang, Y.-R. Zhang, B. Qin, Y.-C. Zhang, Y.-X. Dai, H.-J. Zhu, Y. Wang, J.-X. Zhao, W.-W. Zhang, J. Ji, S.-T. Yuan, Q.-D. Shen, Q.-H. Liu

This study shows that FTO, through lactylation-driven m6A modification of CDK2, worsens diabetic retinopathy by promoting angiogenesis and inflammation, and presents a nanotherapeutic approach to inhibit FTO.

bioRxiv · May 19, 2023 · PreprintCell Biology

D/E-rich peptides are less suitable than D/E-deficient peptides for identification by negative-ion HCD due to scarce production of sequencing ions from multiply charged precursors

M.-Q. Zuo, R.-X. Sun, M.-Q. Dong

The paper shows D/E-rich peptides produce fewer sequencing ions in negative-ion HCD MS, making them harder to identify, and suggests using proteases that generate D/E-deficient peptides for better results.

bioRxiv · Jun 30, 2022Biochemistry