SARomics Biostructures entered an expansive phase and things started to move quickly. Last year may be described by one single word – fantastic! The company employed four new people, new services were introduced, and many new customers found their way to us.
Perhaps one of the most exciting moments was that our newly introduced weak affinity chromatography (WAC) fragment library screening services really started to give results – with the introduction of WAC our integrated drug discovery platform was “discovered” by big pharma as well as smaller biotech companies. We believe that the new screening technology, in combination with the extensive biophysical competence at SARomics Biostructures, will pave the way for us to attack certain classes of drug targets with high innovative potential, notoriously known for the difficulties associated with the identification of new hits/inhibitors against them. Together with our close partner, Red Glead Discovery, we have now full capacity to successfully run fragment-to-lead or gene-to-lead projects.Our screening capabilities using biophysical methods, like protein NMR spectroscopy and other techniques are highly complementary to WAC and may be used, e.g., for the characterization of the binding site and detailed analysis of protein-ligand interactions.
Introduction of biosimilar testing services, including higher-order structure characterization – these services are based on recent advances in NMR spectroscopy that have made it possible to acquire a unique fingerprint representation of the 3D conformation of large molecules like biologics, without expensive isotope labeling. By directly matching the NMR fingerprint of a given protein to its high-resolution three-dimensional structure, we can rapidly assess comparability of a biosimilar and its originator, or different batches of the same biologic. These services are of high value for customers, since FDA registration of biosimilar is much more complicated and more expensive than registration of generic small molecule drugs, and requires more advanced product characterization. With the current growth of the biologics/biosimilars market, we believe that these services will see considerable growth in the coming years.
In addition to the biosimilar testing services, we have “officially” introduced co-crystallization of antigen-antibody complexes. Although we have been doing this for a while and have accumulated extensive experience within the area, we never had a separate page on our web site dedicated to these services. For simplicity and convenience, we have now a separate description of these services for our clients.
Our most popular crystallography services pipeline has also been upgraded: Our off-the-shelf FastLane™ Premium and FastLane™ standard libraries have been complemented with a number of new structures.
Often the crystallography services pipeline is used for co-crystallization of the protein in question with the client’s ligand (or a set of ligands). In the case of gene-to-structure projects, we clone, express, purify and crystallize the protein. In the case of FastLane Premium structures, we normally have the protein stored in the lab and crystallization drops can be set up essentially immediately after the arrival of the ligands. For the FastLane Standard library we have the construct and verified protocols for expression, purification and crystallization of the proteins. In some cases it has taken us only about two weeks from signing the contract with the customer to the three-dimensional structure of the protein complex.
It is well known that the CRO market is in a state of constant expansion. Most small-to-mid-size biotech companies typically lack structural biology capabilities, and often even biophysical competence, since core competences at these companies are normally focused in the fields of biochemistry and molecular biology. SARomics Biostructures’ technology platform is well prepared for meeting these needs by providing reliable data at the best quality level.