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Active NON-SBIR/STTR RPGS NIH (US)

Developing RNP-MaP into a broad-spectrum toolset for discovery, definition, and drug targeting of RNA-protein complexes in live cells

$3.14M USD

Funder NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
Recipient Organization University of Michigan At Ann Arbor
Country United States
Start Date Sep 21, 2024
End Date Aug 31, 2029
Duration 1,805 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10940606
Grant Description

ABSTRACT My laboratory is interested in how interactions between RNA and RNA-binding proteins drive diverse biology and disease, and how these RNA-protein complexes might be targeted to alter their functions. Existing knowledge includes only a small fraction of protein-RNA interactions in the cell, and we know particularly little of how RNA-

binding proteins cooperate to form complexes on noncoding RNAs, which make up the vast majority of human transcripts. Further, while pipelines for identifying protein-binding molecules for therapeutic development are informed by significant understanding of protein structure, there is no existing equivalent for designing small

molecules that target RNA and RNA-binding interfaces. Critically, there remains a lack of straightforward technologies for discovery, definition, and drug targeting of protein-RNA interactions inside cells. To illuminate features of RNA-protein complexes and discover new ways to control their functions, my laboratory

is developing a suite of novel live-cell chemical probing technologies based around my unique RNP-MaP approach (RNA-protein networks analyzed by mutational profiling). By enhancing and modularly extending the base RNP-MaP framework, we will develop new facile methods for 1) mapping multi-protein networks on RNA

across transcriptomes and identifying associated RNA-binding proteins, 2) mapping transcriptome-wide targets of RNA-binding proteins while simultaneously measuring RNA site-specific occupancy, and 3) mapping small molecule RNA-targeting potential inside cells. Our ultimate goal is to create a set of tools that could enable any medical research laboratory to identify,

characterize, and target any RNA-protein interface relevant to their disease/pathway/model of interest. By providing the means to probe the uncharted landscapes of RNA-protein networks, this work will be foundational for expansive new RNA biology discoveries and RNA-targeted therapeutics.

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University of Michigan At Ann Arbor

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