SBIR/STTR Research Award

Targeting RNA to develop novel antibacterial agents

Award identifier 0b3f68b332e8ab29052668563b5b1446477ce276d16d4f3a8dbced7fee008c52Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$152,325

Program and phase

SBIR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
PTC THERAPEUTICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
LH7QEHP9V7W1
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Both the emergence of multidrug resistant bacteria and the further development and deployment of bioterrorism agents emphasizes the urgency for identifying novel antibiotics. PTC Therapeutics, Inc. is a company dedicated to targeting post-transcriptional cellular pathways by identifying small molecule compounds that bind directly to unique regulatory RNA sequences. Bacterial RNase P is a ubiquitous, structurally conserved RNA-based ribozyme that is essential for maturation of tRNA and thus bacterial cell growth. The enzyme is distinct from its eucaryal counterpart, making it an ideal target for the development of small molecule drugs. There are currently no therapies that target this essential catalytic RNA enzyme. The applicants have developed a high throughput FP assay that is robust, reproducible and has been validated against a 3,400 compound library. The investigators propose to screen the PTC's extensive small molecule compound library for inhibitors of Escherichia coli RNase P. Inhibitors of the E. coli enzyme (type A) will be tested against enzymes obtained from Staphylococcus aureus and Bacillus subtilis (both of the type B class). Bacteria predominantly contain either type A or B RNase P, and compounds shown to inhibit both types of enzymes will be characterized by their ability to inhibit growth of vancomycin resistant Enterococci and multidrug resistant Staphylococcus aureus (MRSA). Broad-spectrum inhibitors will be further tested for inhibition of the eucaryal RNase P enzyme and cytotoxicity against a panel of mammalian cell lines.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Research funding history

13 SBIR/STTR records share this UEI (2000–2006). Reported award amounts total $5,224,297. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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