Integrated Core Services

Accelerating Drug Discovery
and Development

The USC Mann School Integrated Core Services, housed in the John Stauffer Pharmaceutical Sciences Center, are your centralized resource on the USC Health Sciences Campus. We provide USC and external investigators with specialized scientific expertise and state-of-the-art technologies to accelerate research in drug discovery and development.

From target identification and high-throughput screening to lead optimization and preclinical evaluation, our Core Labs deliver a comprehensive, end-to-end service pipeline. Each facility is led by experienced PhD-level scientific directors who collaborate closely with USC Mann faculty and affiliates. This unique blend of expertise ensures translational relevance and deep scientific support for academic teams, biotech innovators and industry partners alike.

Fully Integrated Services

Seamless, cost-effective project support with high scientific quality

Cutting-Edge Technology

More than 100 advanced instruments enabling high-throughput workflows

Subject Matter Expertise

PhD-level core directors with extensive experience in pharmaceutical and biotechnology research

Academic Collaboration

Access to the broad expertise of USC Mann faculty across therapeutic areas and research disciplines

  • High-throughput assays and imaging for target discovery and validation
  • Multi-omic and AI analyses to reveal disease mechanisms and targets
  • Custom assay design and expert consultation
  • Human-relevant models such as organ-on-a-chip systems
  • Automated high-throughput screening to identify bioactive hits
  • Mechanisms-of-action studies to define on- and off-target effects
  • Biomarker discovery to inform drug development and patient stratification
  • Generative AI-driven design of novel small molecules, biologics, and other therapeutic modalities
  • Structure-activity and ADMET optimization to improve potency, selectivity and bioavailability
  • Custom synthesis of small molecules, metabolites, and intermediates tailored to project needs
  • Structural characterization of small molecules and biologics using NMR, mass spectrometry and elemental analysis
  • Comprehensive compound profiling to prioritize the most promising candidates
  • Target druggability assessment and library design using commercially available or synthetically feasible scaffolds
  • Structure-based and phenotype-based virtual screenings, including predictions of dynamic binding features and cryptic binding pockets
  • Advanced ADMET and PK/PD profiling to characterize compound behavior and guide dose selection
  • Human-based organ-on-a-chip models to assess drug-induced liver injury (DILI) and overall preclinical safety
  • AI-integrated multi-omic profiling to evaluate therapeutic efficacy and generate holistic mechanistic insights

Contact Us

For specific core inquiries, please contact the core directors directly. For general inquiries about our integrated core services, please fill out the form below. 

Core Directors

Whitaker Cohn, PhD

Multi-Omics Mass Spectrometry Core
wcohn@usc.edu

Zhang-Xu Liu, PhD

Translational Research Laboratory Core
zxliu@usc.edu

Syed Ahmed, PhD

Medicinal Chemistry Core
ahmedsye@usc.edu

FAQ

XXXXXXXXXXXXXXXXXXXXXXXXXXXXX

How will the core support Drug Design and Synthesis?

The USC medicinal chemistry core works with investigators end-to-end, providing consultation and support in both structure-based and ligand-based drug design. The core’s experienced medicinal chemists utilize advanced computational approaches, including glide docking within the Schrödinger software suite and StarDrop for metabolic assessments, followed by synthesis, purification, and complete characterization of the designed compounds.

What is the scope of work that the Core assists with on “hit” identification? 

The core assists with hit identification through both computational and experimental approaches. Computational methods include virtual screening, molecular docking, and pharmacophore modeling to identify potential hit compounds. Experimental approaches involve high-throughput screening (HTS) of chemical libraries against biological targets, fragment-based screening, and biochemical or cell-based assays to detect active compounds. Additional techniques such as surface plasmon resonance (SPR), thermal shift assays, and NMR-based screening are employed to confirm binding interactions and evaluate compound potency. Together, these strategies help validate computational predictions and identify promising hits for further optimization.

Can I get help with Hit-to-Lead and Lead Optimization Chemistry?

The core provides support for both hit-to-lead and lead optimization chemistry. This includes:

  • Design and synthesize analogs to improve potency, selectivity, and drug-like properties
  • Structure-activity relationship (SAR) studies to guide chemical modifications
  • Computational support to predict metabolic stability, solubility, and binding
  • Synthesis, purification, and characterization of optimized compounds
  • Integration with ADME/PK data to guide next-generation compound design

Can the USC Medicinal Chemistry Core assist with ADMET profiling and in vivo PK/PD studies?

The core provides comprehensive support for ADMET (absorption, distribution, metabolism, excretion, and toxicity) profiling and in vivo PK/PD (pharmacokinetic/pharmacodynamic) studies. It helps evaluate a drug candidate’s metabolic stability, bioavailability, clearance, and tissue distribution, generating critical data to guide lead optimization and preclinical development. 

Does this core support small-molecule discovery and patent filing?

Yes. The core supports small-molecule drug discovery and can assist in the development of novel compounds suitable for patent filing.

Does this core provide support with grant-based collaborations? 

The core supports grant-based collaborations by assisting investigators with project planning, budgeting for medicinal chemistry services, and providing letters of support or technical details required for grant applications. The Core’s expertise in drug design, synthesis, and ADMET evaluation can be included as part of collaborative proposals to strengthen funding applications and ensure the feasibility of the proposed research.

What types of molecules can you analyze? 

The core routinely measure small molecules, drugs, metabolites, lipids, and proteins, and can tailor methods for your specific compound or biological question.

How can the core support drug discovery and development studies? 

The core provides support throughout the entire drug development pipeline, from early-stage target identification and high-throughput screening to ADME and pharmacokinetic studies that aid hit-to-lead optimization, all the way through mechanism of action characterization and biomarker discovery.

Can you help determine the mechanism of action of my drug? 

Yes. The core uses a variety of advanced proteomics approaches to identify both direct drug targets and downstream pathway effects, providing a systems-level view of your compound’s mechanism of action.

Can you analyze where my drug goes in the body? 

Absolutely. The core can track drug distribution and metabolism in plasma, tissues, and cells to understand how your compound is absorbed, distributed, and cleared.

Can you help characterize the physicochemical and ADME properties of my drug?

Yes. The core offers assays to evaluate plasma and tissue binding, solubility, cell permeability, and metabolic stability. These studies help predict how your drug behaves in vivo and support lead optimization.

Can you image molecules with a mass spectrometer? 

Yes. Using mass spectrometry imaging, we can visualize the spatial distribution of drugs, metabolites, and other biomolecules directly in tissues, allowing you to see where your compound goes and how it affects the surrounding environment without the need for labels or stains.

How much sample do you need? 

Typically, only a few microliters of biofluid or milligrams of tissue are needed, depending on the analysis. We can help you plan sample collection and preparation.

How long does an analysis take? 

Turnaround times vary with project size, but most studies are completed within 2–4 weeks. Method development or imaging projects may take longer.

How do I get started? 

Just contact the core with a short project description. We’ll schedule a consultation to discuss your goals, sample types, and the best analytical approach.

What services does your core provide?

The translational research core offers user training, assisted use, and expert consultation across a wide range of instruments and applications, including sample processing, cell and immunobiology, flow cytometry, in-vitro and in-vivo imaging, cellular and molecular assays, organ-on-a-chip models, and histology.  

Do you provide services for biomarker identification?

Yes. The core provides comprehensive Luminex and MSD multiplex immunoassay services for cytokine profiling, biomarker discovery, and personalized medicine applications.

Do you provide flow cytometry services?

Yes. The core offers multiparameter flow cytometry services for analyzing cell phenotypes and functions. We also provide sterile cell sorting with high purity and viability for both in-vitro and in-vivo studies.

Do you offer animal-alternative platforms for testing drug toxicity in a human organ-specific environment?

Yes. The core offers a human-based microphysiological system (organ-on-a-chip) to enable human-relevant, organ-specific drug toxicity testing. This platform allows for real-time imaging and multi-omics assays, providing more predictive drug response data than traditional animal models and is particularly valuable for evaluating drug-induced liver toxicity, a major challenge in drug discovery and development.  Other applications with this system include interrogation of disease biology at the organ-specific level.

Do you provide services for studying cellular metabolism in live cells?

Yes. The core provides access to the Agilent Seahorse XFe96 Analyzer, which measures the oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) to assess mitochondrial respiration and glycolytic activity, enabling comprehensive evaluation of cellular metabolic function.

Do you provide imaging services?

Yes. TRCore offers a wide range of imaging services, including the Agilent Cytation 5 cell imager, Keyence BZX all-in-one microscope, Zeiss LSM 880 with Airyscan confocal microscope for high-resolution fluorescence imaging of cells and tissues, and the IVIS Lumina system for in vivo imaging.

USC Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.