TAS::75 0849::TAS OPTION EXERCISE MODIFICATION

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: N44CO090067
Agency Tracking Number: N44CO090067
Amount: $373,298.00
Phase: Phase II
Program: SBIR
Awards Year: 2011
Solicitation Year: 2011
Solicitation Topic Code: NCI
Solicitation Number: N/A
Small Business Information
INTRINSIC BIOPROBES INC.
2155 E CONFERENCE DR STE 104, TEMPE, AZ, 85284-2604
DUNS: 965127038
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 KEMMONS TUBBS
 (480) 804-1778
 KTUBBS@INTRINSICBIO.COM
Business Contact
 KEMMONS TUBBS
Phone: (480) 804-1778
Email: KTUBBS@INTRINSICBIO.COM
Research Institution
 Stub
Abstract
This proposal sets forth a precise and rapid methodology for identifying the interaction sites between monoclonal antibodies and proteins. The basis of the system is a high-throughput mass spectrometry-based analysis of epitope determinants to identify theinteracting protein sequences using immunoaffinity capture combined with enzymatic digestion of the target protein; either pre- or post-capture. This combination will be used to rapidly determine the approximate location of each binding epitope. The precise location of the binding epitope will then be determined by immunoaffinity capture and mass spectrometric readout of sets of synthetic ladder peptides that span the approximate epitope established from the initial analysis. The project will develop reproducible methods to demonstrate epitope mapping for monoclonal antibodies of interest to NCI tested by multiple sampling and quantifiable results. Mapped epitopes will be functionally characterized by amino acid substitutions in the epitope sequence using high-throughput spotted array surface plasmon resonance imaging and SPR-Biomolecular Interaction Analysis to identify the key amino acids that are critically involved in binding the antibody to the antigenic epitope. Thus, this approach will provide an efficient and cost effective platform from which to accomplish high-throughput epitope mapping of monoclonal antibodies for use in diagnosis of cancer.

* information listed above is at the time of submission.

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