Leadership
Thomas R. Fuerst, Ph.D.
Professor, Department of Cell Biology and Molecular Genetics
Director, Center for Glycosylation of Advanced Biologics
Fellow, Institute for Bioscience and Biotechnology Research University of Maryland
Dr. Fuerst is a professor in the Department of Cell Biology and Molecular Genetics, University
of Maryland (UMD), and serves as director of the Center for Glycosylation of Advanced
Biologics (CGAB). He also served as director of the Institute for Bioscience and Biotechnology
Research (IBBR), UMD. Dr. Fuerst has over three decades of research and development
experience in vaccines and therapeutics. At UMD-CGAB, his research is focused on structure-
based vaccine design with an emphasis on hepatitis C virus, scaffold-based protein
therapeutics with an emphasis on cancer targets (RAS-based), precision glycoengineering of
biomolecules with an emphasis on SERPINS (Serine Protease Inhibitors), and an
immunoadjuvant and delivery system centered on a polyphosphazene-based macromolecular
scaffold and Toll-Like Receptor (TLR) agonists. Early in his career, Dr. Fuerst was the founding
scientist of MedImmune (now AstraZeneca) in which he helped to establish its R&D programs.
At MedImmune, his lab was engaged in the development of several products, two of which
have been licensed by the FDA (Synagis, humanized monoclonal antibody to respiratory
syncytial virus, and Cervarix, human papillomavirus vaccine). After the 9/11 attack, he was
asked to join the U.S. Department of Health and Human Services to serve as director, vaccines
and biologics in the Office of the Secretary. In this capacity, he helped establish and lead the
Biomedical Advanced Research and Development Authority (BARDA) responsible for the
development and acquisition of vaccines and immunotherapeutic products for biodefense and
other emerging public health threats. Dr. Fuerst also served as program director of a Defense
Advanced Research Projects Agency (DARPA) initiative for the Department of Defense (DoD)
to develop the concept of a dedicated, flexible capability for the advanced development and
manufacturing (ADM) of biological countermeasures to address national security needs. The
ADM now serves as the basis for HHS and DoD strategic initiatives to enhance domestic-
based development and manufacturing capabilities for biodefense and pandemic flu
preparedness and response. Dr. Fuerst received his training as a senior fellow at the National
Institutes of Health, NIAID, in Bethesda, MD, and holds a BA in biochemistry from the
University of California at Berkeley, a PhD in molecular genetics from Cornell University, and an
MBA in science, technology, and innovation from the George Washington University. He has
authored over 100 publications, recipient of 11 issued patents, received several Distinguished
Service Awards for leadership from HHS, and serves on advisory boards in the biotechnology
industry.
Nathan Lewis, Ph.D.
Professor and GRA Eminent Scholar, Member of the Center for Molecular Medicine
Nathan Lewis is a GRA Eminent Scholar and Professor in
Complex Carbohydrate Research Center, Center for Molecular Medicine, and
Department of Biochemistry and Molecular Biology at the University of Georgia. As the
Co-Director of CGAB, he oversees cell line engineering, automation, and AI systems,
focused on the production of industry-ready cell lines and glycotherapeutics. More
broadly, Prof. Lewis is an expert in biotechnology and computational biology, with
extensive experience in the analysis and design of cell factories and biologics. With
experience in genomics and systems biology, he helped lead the public efforts to
sequence the genomes of the Chinese hamster and diverse CHO cell lines. He
subsequently served as the Scientific Coordinator for the CHO cell engineering program
at the Novo Nordisk Foundation Center for Biosustainability and the National Biologics
Facility at the Technical University of Denmark, wherein his team led the development of
complex systems biology models and A.I. to study and engineer metabolism, protein
secretion, and glycosylation in mammalian cells, and to engineer desired traits into
mammalian production hosts.