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Fabrication of a Multiplexed Artificial Cellular MicroEnvironment Array
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Inferring reaction network structure from single-cell, multiplex data, using toric systems theory.

Shu Wang1,2, Jia-Ren Lin1, Eduardo D Sontag1,3

  • 1Laboratory of Systems Pharmacology, Department of Systems Biology, Harvard Medical School, Boston, Massachusetts, United States of America.

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|December 7, 2019
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Summary
This summary is machine-generated.

We introduce Effective Stoichiometric Spaces (ESS) to reconstruct biochemical networks from single-cell data. This method uses toric geometry to map cell data to chemical reaction network structures.

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Area of Science:

  • Biochemistry
  • Systems Biology
  • Computational Biology

Background:

  • Single-cell studies aim to understand biochemical reactions governing cell fate and state.
  • Reconstructing biochemical networks from complex single-cell data remains a challenge.

Purpose of the Study:

  • Introduce Effective Stoichiometric Spaces (ESS) for biochemical network reconstruction.
  • Leverage toric varieties to analyze single-cell data and infer chemical reaction network (CRN) structure.

Main Methods:

  • Developed the Effective Stoichiometric Spaces (ESS) concept.
  • Applied geometric theory of toric varieties to map data covariances to stoichiometric information.
  • Reframed aspects of CRN theory for enhanced data analysis.

Main Results:

  • ESS provides a data-driven approach to unravel CRN structure.
  • Each cell subpopulation is associated with an ESS interpretable via CRN theory.
  • Successfully processed cytometry and image-based single-cell datasets.

Conclusions:

  • ESS offers a novel framework for single-cell data analysis in systems biology.
  • The method facilitates the identification of differences in cell populations, such as responses to kinase inhibitors.
  • Applicable to data from methods like Fluorescence Activated Cell Sorting (FACS) and multiplex immunofluorescence.