SBIR/STTR Research Award

Integrating microbial signal transduction pathways and their metabolic targets

Award identifier 7b569432eb7e39f9630c82f1c8f9b312c6c284d3626f945ab04a4a80d85e256aAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$99,500

Program and phase

SBIR · Phase I

Award year

2008

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
AGILE GENOMICS, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2007-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Signal transduction systems regulate the majority of cellular activities including the metabolism, development, host-recognition, biofilm production, virulence, and antibiotic resistance of human pathogens. Thus, knowle dge of the proteins and interactions that comprise these communication networks is an essential component to furthering biomedical discovery. The proliferation of genomic data from high-throughput sequencing projects has dramatically accelerated biological discovery, yet there is an ever-increasing need for computational approaches to synthesize meaningful higher-order knowledge from this data. The inherent complexity of signal transduction systems has impeded efforts to elucidate the higher-order prope rties of these critical regulatory networks at the genomic level. The goal of the proposed research is to develop an effective, computational approach for deriving microbial signal transduction pathways from genomic data and linking these systems to their respective regulatory and metabolic targets. The proposed solution to computationally inferring signal transduction pathways involves a bottom-up approach that begins with analyzing signal transduction proteins at the domain level, followed by establishi ng clusters of orthologous domains, and finally grouping functionally associated two-component proteins into pathways using genomic context methods. The final product will be a comprehensive database of microbial signal transduction systems and their assoc iated metabolic networks. Knowledge of the signaling systems responsible for the virulence of human pathogens will promote our understanding of bacteria-host interactions, the immune response, novel antibiotic drug discovery, and therapeutic applications f or treating disease. Because of the critical role of signal transduction in bacteria, this project will significantly impact and contribute to biomedical discovery, public health care, bioremediation, and agriculture.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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