Transforming Lives
Pioneering Enzyme Replacement Therapies for lysosomal storage diseases, using AI and synthetic biology to meet patients' unmet clinical needs.
About ZYTHERA
Next-generation enzyme replacement therapies for lysosomal storage diseases.
ZYTHERA is at the forefront of developing groundbreaking treatments for lysosomal storage diseases (LSDs), a diverse group rare metabolic disorders caused by enzyme deficiencies that lead to the accumulation of harmful substances in cells. Our mission is to transform the lives of patients by delivering highly effective and innovative enzyme replacement therapies (ERT).
We are committed to researching, developing, and commercializing state-of-the-art enzyme replacement therapies that address the unmet medical needs of those suffering from lysosomal storage diseases. Our focus is on delivering therapies that are not only safe and effective but also accessible to patients worldwide.
Our platform
Transforming lives through Advanced Enzyme Replacement Therapies
The ZYTHERA platform combines generative artificial intelligence for protein engineering, with a high-throughput microbial screening platform and downstream mammalian biologics production system to move from computational design to lead candidate identification in as little as 4-weeks.
Our propietary generative AI model uses protein sequence information to learn high-order amino acid relationships to design variant libraries of a target enzyme. Our variants are prioritized using our in-silico characterisation workflows to bring into the lab the most promising candidates.
We have developed a highly efficient, microliter-scale, protein screening platform based on P. pastoris, a widely used yeast in the biotech industry, which allows us to screen hundreds of enzymes in as little as 2 weeks.
Our Chinese Hamster Ovary (CHO) system integrates landing pads at genomic loci, which are designed to ensure single copy genomic integration of target enzymes to facilitate stable production of proteins with human-like biochemical properties.
Our Team
Experts in Next-generation Therapeutics Engineering
Giovanni Stracquadanio, PhD
CEO and Co-founder
Giovanni Stracquadanio, PhD
CEO and Co-founder
Bio
Dr Giovanni Stracquadanio is an Personal Chair in Engineering
Biology at the University of Edinburgh. He is an UKRI EPSRC
fellow and co-director of the Edinburgh Genome Foundry. He has
more than 15 years of experience in AI, computational biology
and microbiology to address biomedical challenges. He was
co-author of the first synthetic eukaryotic chromosome and has
characterised the role of high-frequency inherited mutations
in the p53 pathway. He is now working on engineering new
enzyme replacement therapies for Fabry diseases using AI and
microbial expression systems.
Susan Rosser, PhD
Co-founder
Susan Rosser, PhD
Co-founder
Bio
Dr Susan Rosser is a Professor of Synthetic Biology at the
University of Edinburgh. She is Director of the Edinburgh
Mammalian Synthetic Biology Research Centre, Co-director of
the Edinburgh Genome Foundry. Her research focuses on
developing tools for synthetic biology approaches for pathway
and genome engineering in bacteria, yeast and mammalian cell
systems. The applications of her work include rapid cell line
engineering for biologics production.
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Eve Miller-Hodges, MD PhD
Medical Advisor
Eve Miller-Hodges, MD PhD
Medical Advisor
Bio
Eve Miller-Hodges is a Senior Clinical Lecturer in Inherited
Metabolic Disorders and Renal Medicine at the University of
Edinburgh with experience across all aspects of translational
research, including developmental biology, clinical trials and
data science. She helped establish clinical care for LSD
patients in Scotland and now works in the Scottish Inherited
Metabolic Disorders Service which provides specialist
management of all patients with lysosomal storage disorders in
Scotland.
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Michelle Levene
Commercial Champion
Michelle Levene
Commercial Champion
Bio
Michelle Levene is Commercial Champion at Zythera, leading
commercial strategy and business development. With over 20
years of experience in life sciences, Michelle has delivered
successful clinical development programs, managed rare disease
product launches, driven cross-functional teams, and supported
major acquisitions and spin-outs. She is passionate about
building partnerships that enable patient access to
transformative treatments and excels at navigating complex
commercial challenges.
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Research
Our ground-breaking research
ZYTHERA stems from ground-breaking research conducted in the Stracquadanio and Rosser lab at the University of Edinburgh and published in international, high-impact, peer-reviewed journals
Dirichlet latent modelling enables effective learning and sampling of the functional protein design space
Lobzaev, E. and Stracquadanio, G., 2024. Nature Communications, 15(1), p.9309.
Protein engineering using variational free energy approximation
Lobzaev, E., Herrera, M.A., Kasprzyk, M. and Stracquadanio, G., 2024. Nature Communications, 15(1), p.10447.