Oxford, UK 12 December 2017: ProImmune, a leader in services for understanding immune responses, today announced the introduction of MutaMap™, a new high-throughput assay service for understanding the impact of point mutations on protein therapeutic activity, including monoclonal antibodies. MutaMap provides a high-throughput service, with high-quality output data, to help decide which individual point mutations to pursue and enable better protein engineering decisions to be made, prior to committing a drug candidate to a clinical program.
MutaMap can deliver a high-throughput mutagenesis project for exploring 500-2000 mutations in approximately 8-12 weeks and deliver a heat map for the protein sequence of interest, showing which point mutations lead to an increase, decrease, or no change in affinity (or other activity), or non-function of the protein of interest when interacting with one, or more, of its binding partners. This effectively reveals which mutations are likely permissible or favourable for protein engineering and provides a novel tool for making informed decisions across a range of key developability objectives. These can include cherry picking mutations to improve activity, de-immunization, altering cross-species reactivity, improved humanization or provision of other engineered features, stability and manufacturability, prolonging half-life and developing unique new composition of matter IP.
MutaMap is the first service ProImmune is offering in the area of protein engineering. The technology is complementary to the company’s existing technologies for assessing the antigenicity of therapeutic proteins and can be readily combined with ProImmune’s leading ProMap® and ProScern® T cell assays, ProPresent® Antigen Presentation Assays and ProImmune REVEAL® MHC-peptide binding assays.
Nikolai Schwabe, CEO of ProImmune, commented: “MutaMap is a key new service in our portfolio that addresses a major unmet need for our customers to make informed protein engineering decisions on a broad range of developability issues such as managing the immunogenicity risk of therapeutic proteins, with confidence that the function of the candidate protein will be maintained or even be improved.”
For further information visit www.proimmune.com.