An RNA targeted platform for anti flavivirus drug discovery

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R43AI129095-01A1
Agency Tracking Number: R43AI129095
Amount: $224,475.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: NIAID
Solicitation Number: PA16-302
Timeline
Solicitation Year: 2016
Award Year: 2017
Award Start Date (Proposal Award Date): 2017-04-01
Award End Date (Contract End Date): 2018-12-31
Small Business Information
606 BOLIN CREEK DR, Carrboro, NC, 27510-1263
DUNS: 079564177
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 KATHERINE WARNER
 (919) 500-8864
 kwarner@ribometrix.com
Business Contact
 KEVIN WEEKS
Phone: (919) 404-7426
Email: admin@ribometrix.com
Research Institution
N/A
Abstract
SUMMARY Emerging and re emerging mosquito borne flaviviruses cause widespread mortality morbidity and economic burden Options for prevention and treatment of mosquito borne flaviviruses are limited Flavivirus vaccines face unique development challenges no antiviral therapies are available and the mosquito vectors have proven difficult to eradicate Despite vaccines against Yellow Fever and Japanese encephalitis viruses these two flaviviruses together cause more than deaths each year Half of the world s population is at risk of Dengue virus DENV infection and emerging flaviviruses including the Zika virus pose significant public health challenges RNA is a compelling target for small molecule drug discovery and the genomes of RNA viruses such as flaviviruses contain highly conserved targetable structures Multiple natural products target ribosomal RNA establishing proof of concept for RNA as a drug target however RNA targeted drug discovery remains a nascent field Specific tertiary structures in the DENV RNA genome have recently been shown to be essential for viral replication These structures are highly conserved across mosquito borne flaviviruses and interfering with their formation inhibits packaging and replication suggesting that small molecules that disrupt these RNA motifs will have broad spectrum antiflaviviral activity At Ribometrix our lead discovery platform combines a very rapid and high throughput initial screen with a secondary assay based on SHAPE technology the gold standard for RNA structure analyses We plan to apply our platform to identify small molecules with favorable medicinal chemistry properties that bind to and disrupt the structure of essential DENV RNA motifs These lead compounds will serve as the foundation for the development of anti DENV and broad spectrum antiflaviviral therapies in a Phase project RNAs share broadly similar overall properties so a strategy that allows RNA to be targeted efficiently in a single case will likely allow targeting of diverse therapeutically important RNAs The long term vision of Ribometrix is to apply this platform technology to discover small molecule therapeutics that target functional RNA structures involved in indications for which there are no approved therapies With this study we will establish proof of principle for an efficient and generic approach for RNA targeted ligand discovery NARRATIVE Mosquito borne flaviviruses pose a significant threat to human health but flavivirus vaccines face unique development challenges no therapies are available and the mosquito vectors have proven difficult to eradicate We propose to identify small molecules that bind to highly conserved structures in the Dengue virus genomic RNA using the Ribometrix lead discovery platform which combines a high throughput initial screen of fragment based libraries with innovative SHAPE MaP technology Disruption of the targeted RNA structures should prevent viral replication and future work will advance the compounds identified in this project into a lead optimization program

* Information listed above is at the time of submission. *

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