SBIR/STTR Research Award
BACTERIAL RNASE P AS A TARGET FOR NOVEL ANTIMICROBIALS
Award amount
$98,975Program and phase
SBIR · Phase IAward year
2002Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- MESSAGE PHARMACEUTICALS, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant): Antibiotic resistance is a growing health
threat worldwide. Small-molecule screens that target specific complexes that
are essential for bacterial metabolism will be useful in identifying new
classes of microbial inhibitors. Bacterial RNase P represents an excellent
target for developing novel anti-infectives: it is essential for viability of
bacteria; it is well-characterized enzymatically and structurally; and it
differs structurally and functionally from mammalian RNase P. Message
Pharmaceuticals is dedicated to developing drugs that target RNA via
post-transcriptional regulation. With its high-throughput capacity, Message has
screened nearly 150,000 compounds for inhibitors of Neisseria gonorrhoeae RNase
P. More than fifty compounds among six classes have exhibited dose-dependent
inhibition of N. gonorrhoeae RNase P in vitro. Message proposes to develop
these classes of leads further by: 1) determining their minimal inhibitory
concentration endpoint against known bacterial isolates; 2) measuring the
inhibition of RNase P enzymes from other evolutionarily diverse pathogenic
bacteria; 3) comparing the inhibition to that of human RNase P; 4) assessing
cytotoxicity in mammalian cells in culture. In addition to identifying novel
anti-infectives, the results will advance our understanding of the function of
an evolutionarily ancient RNA enzyme, and, more importantly, reveal new classes
of small molecules that interact with structured RNAs.
PROPOSED COMMERCIAL APPLICATION:
With the worldwide emergence and expansion of antibiotic resistance in both the nosocomial and community settings, new classes of antibiotics are needed to combat the resistance. The results from this grant will contribute to the development of novel classes of antibiotics for a variety of resistant bacterial infections.
Technology keywords
Not reported