Decoding Cardiovascular Disease Through Spatial Proteomics

Min Ma1,2, Yingyi Lian1, Erfei Shang3

  • 1Department of Pharmaceutical Sciences (M.M., Y.L., C.X., M.Z., J.Q.), University at Buffalo, NY.

Circulation Research
|July 30, 2026
PubMed

Insights

Spatial proteomics reveals how protein organization in cardiovascular tissues impacts health and disease. Integrating tissue mapping and region-specific analysis offers deeper insights into complex cardiovascular biology.

Area of Science:

  • Cardiovascular Biology
  • Proteomics
  • Spatial Biology

Background:

  • Cardiovascular function relies on intricate tissue architectures, including cell and extracellular matrix organization.
  • Spatial proteomics is crucial for understanding cardiovascular biology and disease by mapping protein distribution.
  • Existing spatial proteomics methods vary in scope, from localized analysis to broad tissue mapping.

Purpose of the Study:

  • To review spatial proteomics strategies applicable to cardiovascular research.
  • To discuss the strengths and limitations of different spatial proteomics technologies.
  • To propose an integrated workflow for comprehensive cardiovascular tissue analysis.

Main Methods:

  • Categorization of spatial proteomics into region-of-interest (ROI)-based and tissue mapping approaches.
  • Evaluation of technologies based on molecular depth, spatial coverage, and spatial resolution.
  • Proposal of a sequential workflow combining untargeted tissue mapping with targeted ROI analysis.

Main Results:

  • Neither tissue mapping nor ROI-based methods alone fully capture cardiovascular tissue complexity.
  • An integrated approach leverages the complementary strengths of both mapping and ROI strategies.
  • This integrated workflow provides multiscale insights into spatially organized cardiovascular disease processes.

Conclusions:

  • Comprehensive understanding of cardiovascular tissue requires both broad spatial organization and localized molecular detail.
  • An integrated workflow using untargeted mapping followed by targeted validation is proposed.
  • This approach enhances mechanistic insights into cardiovascular biology and disease.

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