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Exploring drug mechanisms through single-cell proteomics

  • Yuzhi Sun
  • , Renjie Liu*
  • , Jichong Mu
  • , Liyuan Zhang
  • , Yadong Wang*
  • *Corresponding author for this work
  • Faculty of Computing, Harbin Institute of Technology
  • Harbin Institute of Technology

Research output: Contribution to journalReview articlepeer-review

Abstract

Drug discovery requires precise mechanistic insights, hindered by traditional bulk omics masking cellular heterogeneity. Single-cell proteomics (SCP) overcomes this by directly quantifying proteins—the cell's functional executors—enabling high-resolution analysis of drug action. This review details how SCP shifts research from the transcriptome to the proteome, covering key methods like high-sensitivity mass spectrometry and data-independent acquisition that now quantify thousands of proteins per cell. We highlight SCP's unique advantages in directly capturing drug targets, modifications, and pathway activity. Translational applications demonstrate its potential in target discovery, elucidation of resistance mechanisms and precision therapy. Finally, the integration of AI with SCP is poised to usher in a new era of protein-centred, high-resolution drug discovery.

Original languageEnglish
JournalBritish Journal of Pharmacology
DOIs
StateAccepted/In press - 2026
Externally publishedYes

Keywords

  • drug mechanisms
  • single-cell mass spectrometry
  • single-cell proteomics
  • single-cell sequencing

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