JURA Bio


Developer of an integrated AI-native drug discovery stack that combines manufacturing-aware generative sequence models, large-scale DNA library synthesis, high-throughput human-cell functional screening, and machine learning training objectives designed to learn from these wet-lab datasets. The platform focuses on discovering immune-based therapeutics (TCRs, TCR-mimicking antibodies, CAR candidates) by co-designing experimental data generation and predictive/causal models.

Industries

biotechnology
genetics
health-care
life-science
therapeutics

Nr. of Employees

small (1-50)

JURA Bio

100 Morrissey Boulevard, Boston, MA 02125


Patents

Major histocompatibility complex-based chimeric receptors and uses thereof for treating autoimmune diseases

US-12421293-B2

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Major histocompatibility complex-based chimeric receptors and uses thereof for treating autoimmune diseases

US-11826385-B2

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Products

Synthesized human antibody and TCR candidate libraries

Large, in-distribution libraries of human-like antibody CDRs and TCR candidates generated by manufacturing-aware models and physically synthesized for screening.


Services

Collaborative research that combines generative sequence design, scaled synthesis, and high-throughput human-cell screening to generate training datasets and discover receptor/antibody candidates.

Design and manufacture of massive synthetic sequence libraries from generative models and downstream screening in engineered human cells with single-cell readouts.

Expertise Areas

  • Generative protein and sequence design
  • High-throughput DNA library synthesis and manufacture
  • High-throughput functional screening in human cells
  • Sequence-to-activity predictive modeling (CNNs, transformers)
  • Show More (6)

Key Technologies

  • Manufacturing-aware generative models
  • High-throughput DNA synthesis
  • Single-cell sequencing
  • DNA-barcoded antigen assays
  • Show More (5)

News & Updates

Research partnership to apply machine learning and synthetic libraries to discover antigen-specific TCRs for development of TCR-NK cell therapies; JURA to receive research funding, milestone and option payments.

Description of LeaVS, a library-aware training objective and experimental-design approach for learning sequence-to-activity maps from measurement-limited screens.

Overview of the VISTA system for creating large, in vitro datasets by steering synthesis and screening with AI models to train therapeutics-focused predictors and generative models.

Introduction of variational synthesis, a manufacturing-aware generative architecture for producing designs that can be synthesized at massive scale and for producing synthesis instructions.

Presentation of CAIRE, a causal estimation method that uses repertoire sequencing and clinical outcomes to infer effects of TCRs on patient outcomes and to prioritize therapeutic candidates.

Produced >1,000 diverse candidate scFv-CARs with specified binding against clinically relevant peptide–HLA targets and validated humanness and specificity metrics in human-cell assays.


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