SBIR-STTR Award

Assigning Protein Functions For The Tuberculosis Genome
Award last edited on: 3/5/07

Sponsored Program
SBIR
Awarding Agency
NIH : NIAID
Total Award Amount
$590,304
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Matteo Pellegrini

Company Information

Protein Pathways Inc

1145 Gayley Avenue Suite 304
Los Angeles, CA 90024
   (310) 208-8444
   N/A
   www.proteinpathways.com
Location: Single
Congr. District: 33
County: Los Angeles

Phase I

Contract Number: 1R43AI047533-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2000
Phase I Amount
$98,306
New proprietary computational methods will be applied to assign biological functions to novel proteins in the genome of Mycobacterium tuberculosis, the causative agent of tuberculosis. Traditional computational methods can only assign functions to genome sequences that are homologs of other previously characterized proteins. The new algorithms developed by Protein Pathways, Inc. use other types of information derived from transgenomic analysis to assign functions to proteins that cannot be characterized by traditional computational methods. The methods will assign probable functions to as many as 1,000 uncharacterized TB protein sequences. Many of the proteins will be identified as having roles in virulence and will therefore be attractive targets for future drug development efforts.

Phase II

Contract Number: 2R44AI047533-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2001
(last award dollars: 2002)
Phase II Amount
$491,998

We propose to apply new proprietary computational methods to assign biological functions to novel proteins in the genome of Mycobacterium tuberculosis, the causative agent of TB. Traditional computational methods can only assign functions to genome sequences that are homologs of other previously characterized proteins. The new algorithms developed by Protein Pathways scientists use other types of information, derived from trans-genome analyses, to assign functions to proteins that cannot be characterized by traditional computational methods. The methods will assign probable functions to as many as 1,000 uncharacterized TB protein sequences. Many of these proteins will be identified as having roles in virulence and will therefore be attractive targets for future drug development efforts. PROPOSED COMMERCIAL APPLICATION: The world-wide emergence of multi-drug resistant strains of many common pathogens calls for new antibiotics. The work proposed here will identify the functions of many previously uncharacterized proteins in the genomes of serveral pathogens, including Staphylococcus aureus and Enterococcus faecalis. Those with roles related to virulence will serve as new, previously unknown targets for therapeutic drugs. Once experimentally validated, these targets will be marketed to our pharmeceutical customers and partners.