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Active CONTINUING GRANT National Science Foundation (US)

CAREER: Enabling next era nucleic acid biotechnology through XNA sequencing

$3.21M USD

Funder National Science Foundation (US)
Recipient Organization University of Washington
Country United States
Start Date Sep 01, 2025
End Date Aug 31, 2030
Duration 1,825 days
Number of Grantees 1
Roles Principal Investigator
Data Source National Science Foundation (US)
Grant ID 2440857
Grant Description

The project develops tools to read expanded genetic alphabets that contain bases other than A, T, G, and C, and studies how natural biological systems interact with these unnatural DNA letters. This research contributes to transformative applications in nucleic acid biotechnology, and has the potential to improve diagnostic assays, lead to the discovery of novel therapeutics, and enhance biomanufacturing techniques.

The project integrates these research activities with robust educational objectives: preparing a globally competitive workforce through workshops for industry professionals, fostering public engagement with hands-on community activities, and developing online resources for data science education. Graduate and undergraduate students participating in the project will gain valuable skills and mentorship experience, contributing to STEM workforce development.

This research addresses key challenges in expanded genetic alphabets, focusing on three objectives. First, it aims to improve generalizability (and accuracy) of next generation sequencing for unnatural base pairs through deep learning. Second, it develops single-context sequencing models that enable high accuracy measurements of polymerase replication fidelity for unnatural bases.

With this new methodology, the project measures polymerases replication fidelity of various polymerase for these unnatural bases in various model in vitro systems - such as PCR and LAMP. Lastly, the project investigates the biocompatibility of unnatural base pairs in a microbial host by examining metabolic processes, replication fidelity, error repair pathways, and host responses.

These approaches promise to bridge key technological gaps and knowledge gaps in expanded genetic alphabets, helping bridge this area of research towards transformative applications in biotechnology.

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

All Grantees

University of Washington

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