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Real-Time Pathogen-Host Interactome Prediction

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DPA26BZ03-DV014SBIR / STTR

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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The contract seeks to develop a computational system capable of rapidly characterizing novel or emerging pathogens—viruses, bacteria, and parasites—using only their protein sequence data, eliminating the need for weeks or months of experimental work. The system must accurately predict protein-protein interactions between pathogens and human hosts across all three pathogen classes, with zero-shot learning capabilities to generalize to previously unseen threats without prior exposure in training data. It must provide detailed functional annotations for both pathogen and host proteins, automatically generate ranked mechanistic hypotheses about infection pathways, and deliver core predictions within 15 minutes and full characterization reports within one hour using standard computing hardware. Rigorous validation is required to ensure the system does not simply memorize known data but can truly generalize, with performance benchmarks against established protein interaction databases and experimental confirmation via standard binding assays. The initiative, titled Real-Time Pathogen-Host Interactome Prediction under solicitation DPA26BZ03-DV014, is issued by the Defense Advanced Research Projects Agency within the Department of Defense to address critical delays in therapeutic response to biological threats. The effort is structured as a total small business set-aside, limited to entities with fewer than 500 employees, aligning with SBIR/STTR mandates. The system must be operationally deployable in real-world defense and public health scenarios to enable rapid prioritization of medical countermeasures and enhance force health protection. Proposals must demonstrate not only technical feasibility but also robust evaluation methodologies and the ability to operate effectively under standard computational environments, ensuring accessibility and scalability for urgent response operations.

General Info

Develop real-time pathogen-host interaction predictor using protein sequences with zero-shot learning, deployable on standard hardware within 15 minutes.

Agency

Department of Defense → Defense Advanced Research Projects AgencyView Agency

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology) View NAICS

Place of Performance

Not specified

Set-Aside

SBA

Documents

(0)

No documents available

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Timeline

PhaseSolicitation
Posted

Solicitation

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Submission deadline

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Organization & Contact Information

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AgencyDepartment of Defense → Defense Advanced Research Projects Agency
ContactsNo contacts available
OfficeUS
Organization / Agency
Department of Defense → Defense Advanced Research Projects Agency
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Office AddressUS
ContactsNo contact information available

Full Description

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When novel or emerging pathogens (bacteria, viruses, parasites) are encountered, characterization of their interactions with human hosts currently requires weeks to months of experimental work, often yielding incomplete understanding. This capability gap limits rapid therapeutic response and countermeasure development. Recent advances in protein language models and large-scale protein-protein interaction (PPI) prediction make computational threat characterization feasible. This topic seeks to develop and validate an operationally deployable capability that can characterize any pathogen—naturally emerging, accidentally released, or engineered—from protein sequence data alone. The system must: (1) predict host-pathogen protein interactions with high accuracy across viral, bacterial, and parasitic pathogen classes; (2) demonstrate zero-shot prediction capability on previously unseen pathogens; (3) provide comprehensive functional annotation of both pathogen and host proteins; (4) generate ranked mechanistic hypotheses about infection pathways through automated analysis; and (5) complete core predictions within 15 minutes and full characterization reports within one hour on standard computing hardware. Proposers must demonstrate rigorous evaluation methods to ensure the system generalizes to unseen pathogens rather than memorizing training data. Performance must be benchmarked against established protein interaction databases and validated experimentally using standard binding assay techniques. The end-state capability enables rapid biological threat characterization to support medical countermeasure prioritization and force health protection.

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