Paper
28 July 2000 Improved approach to RNA and protein recognition for pathogen detection
Brian N. Zeiler, Burt V. Bronk, Abraham Grossman
Author Affiliations +
Abstract
We are developing (U.S. Air Force, SBIR) a proprietary technology, based on the enzyme Q-beta replicase, to very rapidly detect and identify microorganisms (rRNA), virions (particularly RNA-based), and proteins of interest for pathogen detection. This enzyme is known to amplify a specific RNA signal one billion-fold in less than fifteen minutes at a constant temperature of 37 degree(s)C. RNA probes are made in `halves' that are joined to each other after their terminal ends are brought into proximity mediated by the binding to the target. Only such a full-length molecule can be amplified. We have demonstrated specific examples of recognition of RNA target sequences of interest in species of Bacillus and are investigating methods for overcoming the well-known promiscuity of the enzyme so that this recognition feature can be utilized with confidence, even in the presence of dirty backgrounds.
© (2000) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Brian N. Zeiler, Burt V. Bronk, and Abraham Grossman "Improved approach to RNA and protein recognition for pathogen detection", Proc. SPIE 4036, Chemical and Biological Sensing, (28 July 2000); https://doi.org/10.1117/12.394055
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KEYWORDS
Proteins

Molecules

Sensors

Target detection

Pathogens

Binary data

Polymers

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