Exscientia Expands Biologics Design Capability with Automated Laboratory
Exscientia (NASDAQ: EXAI) has announced the launch of an automated biologics laboratory in Oxford, enhancing its platform to design human antibodies. This development follows AI advancements in virtual biologics design and aims to integrate AI with high-throughput profiling. The laboratory will allow Exscientia to create optimized antibodies rapidly, tapping into a database of paired human antibody sequences. The goal is to revolutionize biologic drug discovery, potentially doubling the target market as antibodies are prominent in top-selling drugs.
- Launch of an automated biologics laboratory in Oxford to enhance antibody design capabilities.
- Expansion into biologics expected to nearly double Exscientia's target market.
- AI-driven methods promise faster and more accurate antibody design compared to traditional approaches.
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Fast and accurate generative AI design of novel antibodies extends
Sequencing paired human antibody data to create better AI models for antibody design
Automated laboratory with proprietary hardware to enable integration of AI design with high-throughput biologics profiling under development
“Exscientia is integrating biologics design into the modular architecture of our end-to-end, patient-first AI platform. Having demonstrated the ability of our existing precision medicine patient tissue models to analyse novel antibodies, we believe the addition of this biologics design capability will create one of the most powerful antibody platforms available,” said Professor
Current approaches to optimise antibodies, even those that use machine learning, still depend on discovering antibodies by experimental screening methods. Combining generative AI design and virtual screening of biologics would allow investigation of a broader antibody space and support Exscientia’s goal to design all of its biologics de novo for specific target epitopes without the need for screening.
In order to design novel antibodies against specific protein epitopes, it is necessary to generate accurate models of their structure at speed and scale. Initial versions of the technology invented by Professor
Key to Exscientia’s AI approach is using the knowledge of the observed human antibody space to optimise biologics for clinical development. The binding site of the antibody consists of two chains (heavy and light). Typically, sequencing of antibodies has been limited to single chains, losing the true biology of antibodies. The Company is building a proprietary database of paired chain sequences to better understand the complex biology of antibodies in a more natural environment.
Exscientia’s new laboratory facilities, which add an additional 8,000 square feet to its headquarters in the
“Our strategy is to replace current experimental discovery techniques with precision engineered de novo design of optimised, fully-human biologics,” said Professor
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Forward-Looking Statements
This press release contains certain forward-looking statements within the meaning of the “safe harbour” provisions of the Private Securities Litigation Reform Act of 1995, including statements with regard to Exscientia’s expectations for the progress of development of candidate molecules; timing and progress of, and data reported from, preclinical studies and clinical trials of Exscientia’s product candidates; Exscientia’s ability to generate novel insights into antibody design and to build hardware and other systems to support high-throughput biologics profiling; and Exscientia’s expectations regarding the expansion of its precision medicine platform and AI-driven drug discovery platform. Words such as “anticipates,” "believes," “expects,” "intends," "projects," "anticipates," and "future" or similar expressions are intended to identify forward-looking statements. These forward-looking statements are subject to the uncertainties inherent in predicting future results and conditions, including the scope, progress and expansion of Exscientia’s product development efforts; the initiation, scope and progress of Exscientia’s and its partners’ clinical trials and ramifications for the cost thereof; clinical, scientific, regulatory and technical developments; and those inherent in the process of discovering, developing and commercialising product candidates that are safe and effective for use as human therapeutics, and in the endeavour of building a business around such product candidates.
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