TOPIC 229: PHASE I AMPK DEV. OF MOLECULAR PHARMACODYNAMIC ASSAYS

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$149,995.00
Award Year:
2008
Program:
SBIR
Phase:
Phase I
Contract:
N43CM0800052
Award Id:
94171
Agency Tracking Number:
N43CM0800052
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
BIOASSAY SYSTEMS, LLC, 3423 INVESTMENT BLVD, STE 11, HAYWARD, CA, 94545
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
174630215
Principal Investigator:
FRANK HUANG
() -
Business Contact:
() -
Research Institution:
n/a
Abstract
AMP-activated protein kinase (AMPK) is a serine/threonine kinase that is a member of a metabolite sensing protein kinase family. AMPK is involved in controlling cellular metabolism and cell proliferation and when activated has been found to be a potent tum or suppressor. Despite a lot of progress in the discovery of therapeutic agents, a pharmacodynamic assay for AMPK is missing. In this proposed research, BioAssay Systems aims to develop a rapid, sensitive, robust and rigorous assay for AMPK activity in tis sue extract. In the Phase I period, BioAssay Systems will select a suitable pan antibody and coat it onto 96-well plates. The immobilized antibody will capture all AMPK protein and isolate it from any potentially interfering enzymes such as other kinases a nd phosphatases. The captured AMPK remains active so that its activity will be directly measured using a fluorescence technology. At the end of the Phase I period, BioAssay Systems will have established experimental conditions and characterized assay perfo rmance including detection limit, reagent stability, reproducibility, variation and accuracy. The SOP of the research pharmacodynamic assay for AMPK will be delivered to NCI. In the Phase II period, BioAssay Systems will further validate the assay in vario us normal and multiple tumor tissues. Studies will be performed to correlate results in tumor versus surrogate tissues such as blood, serum or plasma. Correlation studies will also be compared in human versus laboratory animals (e.g., mouse and rat). This proposal presents a generic platform technology, the successful development and application of which will allow BioAssay Systems to rapidly develop pharmacodynamic assays for other important cancer targets such as kinases, phosphatases and proteases of int erest to NCI.

* information listed above is at the time of submission.

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