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Catalytic Antibodies for Chemiluminescence Enhancement

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: N/A
Agency Tracking Number: 22244
Amount: $50,000.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Timeline
Solicitation Year: N/A
Award Year: 1993
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
4131 Lakeside Drive, Suite B
Richmond, CA 94806
United States
DUNS: N/A
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 Krishna Balakrishnan
 (510) 222-4940
Business Contact
Phone: () -
Research Institution
N/A
Abstract

Chemiluminescent (CL) reactions suffer from low quantum yields because of competing dark reaction pathways; this can be overcome, if the excited state emitter can be stabilized. A monoclonal antibody raised against an appropriately designed target structure (one that closely resembles the excited state emitter) may serve as a surrogate binding molecule. The resultant enhanced CL can then be extremely useful in a variety of applications, e. g. immunoassays. The luminol peroxide reaction is one of the most widely utilized CL reactions. If the antibodies are raised against 3-aminophthalate (APA), then the excited state emitter can be expected to enhance CL yield. In Phase I efforts, several monoclonal antibodies to the APA hapten will be developed, and their usefulness as CL enhancers will be examined. Additionally, anti- APA IgM secreting clones developed in earlier efforts will be manipulated to generate anti-APA IgG antibodies. The usefulness of all these antibodies will also be examined in the related isoluminol reaction. In Phase II studies, a larger bank of catalytic antibodies for these CL reactions as well as other reactions such as the acridinium ester reaction will be generated. The usefulness of all these catalytic antibodies in prototype immunoassays will also be examined, thus paving the way for commercial exploitation.

* Information listed above is at the time of submission. *

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