Glycosaminoglycans (GAGs) are involved in a plethora of diseases such as inflammation,
fibrinogenesis, wound healing, oncology & metastasis, blood coagulation, MI & restenosis, MS &
neurodegeneration. These highly charged and linear polysaccharides represent a novel class of
therapeutic targets which cannot be explored by biologics such as monoclonal antibodies because
of the lack of suitable and specific antigens. We are therefore using the recognition sites of natural
GAG-binding proteins and engineer them towards high affinity ligand binding. For this purpose
we have generated a unique library of human GAG oligosaccharides which are used for screening
and optimising our GAGbodies™. Target specificity and off-target effects are tested by our ELICO
technology. We have collected the large pool of all GAG-binding proteins in our GlycAffibaseTM which
provides the basis for our directed GAGbody™ engineering.
Antagonis is located in a research-driven environment on the Campus of the Karl Franzens-University
Graz where internationally recognised GAG research has been successfully ongoing over the last
ten years, which was funded by national and international public organisations as well as by private
venture capital. Antagonis has a close collaboration with a local manufacturer who provides the
Pichia pastoris expression expertise as well as the scaffolding technology for serum half life extension
of our GAGbodies™. Although Antagonis is positioned as a platform company our lead product is an
MCP-1-based GAGbody™ which shows excellent activity in a murine metastasis model.