chandrasekaran-headshot

Sriram Chandrasekaran, Ph.D.

Associate Professor, Biomedical Engineering, and Associate Chair for Research in Biomedical Engineering

Location

NCRC, Building 520, Room 3328
1600 Huron Parkway
Ann Arbor, MI 48109

Phone

(734) 764-1566

Primary Website

Systems Biology Lab

Research Interests

  • Fighting drug resistance using AI:  We are developing mechanistic AI tools (e.g. INDIGO, MAGENTA, CARAMEL) to design drug combinations with enhanced potency and reduced potential for developing resistance. We also study pathogen metabolism and pathogen-immune interactions to discover new synergistic antibiotics against M. tuberculosis, S. aureus and other pathogens.
  • Systems biology methods for simulating metabolic regulation: Our lab is developing new modeling tools to simulate the activity of thousands of metabolic reactions in a human or microbial cell, providing a unique systems perspective on metabolic regulation. We have applied the methods that we developed (e.g. PROM, DFA, GEMINI, RECON8D, and ASTRIX) to understand microbial, stem-cell, cancer, and brain metabolism using omics datasets.

Research Areas:

Biomedical Computation and Modeling, Cancer, Drug Delivery and Therapeutics, Tissue Engineering and Biomaterials, Tissue Engineering and Regenerative Medicine

Teaching

  • AI in BME (BME 487): This course introduces students to AI and machine-learning algorithms and their applications in BME. The course is open to both graduate and undergraduate students. Learn more at the course website: https://systemsbiologylab.org/ai-bme-syllabus

Publications

  • A structural machine learning approach for rapid prediction of thermodynamically destabilizing tyrosine phosphorylations. Cell Reports Methods 2025.
  • Inferring Metabolic Objectives and Tradeoffs in Single Cells During Embryogenesis, Cell Systems, 2025.
  • A flux-based machine learning model to simulate the impact of pathogen metabolic heterogeneity on drug interactions. PNAS Nexus, 2022.
  • Genome-scale network model of metabolism and histone acetylation reveals metabolic dependencies of histone deacetylase inhibitors, Genome Biology, 2019
  • Transcriptomic signatures predict regulators of drug synergy and clinical regimen efficacy against Tuberculosis, mBio, 2019
  • Comprehensive mapping of pluripotent stem cell metabolism using dynamic genome-scale network modeling, Cell Reports, 2017
  • Granzyme B disrupts central metabolism and protein synthesis in bacteria to promote an immune cell death program, Cell, 2017

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