Advanced training platform and methodologies for emergency responders and skilled

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$216,247.00
Award Year:
2013
Program:
SBIR
Phase:
Phase I
Contract:
1R43AI102326-01A1
Agency Tracking Number:
R43AI102326
Solicitation Year:
2013
Solicitation Topic Code:
NIAID
Solicitation Number:
PA12-088
Small Business Information
PARATECHS CORP.
1122 Oak Hill Dr., LEXINGTON, KY, -
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
178801671
Principal Investigator:
ANGELIKA FATH-GOODIN
(859) 317-9213
agoodin@paratechs.com
Business Contact:
ANGELIKA GOODIN
(859) 317-9213
agoodin@paratechs.com
Research Institution:
Stub




Abstract
DESCRIPTION (provided by applicant): The baculovirus expression vector system (BEVS) has been successfully utilized to produce thousands of proteins for use as vaccines, therapeutics, and for structure-function studies. One limitation of BEVS is the propensity of baculoviruses to accumulate transposon insertions into the fp25k gene leading to the few polyhedra (FP) phenotype. This mutation shifts the balance of virus production from occlusion-derived viruses, which are not infectious in tissue culture, tobudded viruses, which are the form of virus that is used in baculovirus expression. These higher levels of budded virus would be advantageous for BEVS users, but FP mutants are also deficient in transcription from the polyhedrin promoter, which drives expression of target genes. Baculoviruses also rapidly accumulate defective interfering particles (DIP), which are linked to a sharp decrease in target gene expression due to deletion of the target gene and/or viral genes needed for its expression. One factorthat promotes DIP formation is transposition into fp25k. The goal of this project is to develop baculovirus expression vectors that allow for manipulation of the fp25k gene. By reducing or eliminating expression of FP25K during virus amplification, we expect to obtain 5- to10- fold higher levels of budded virus titers because most of the replicative potential of the cel would go to producing budded virus instead of occlusion-derived virus. Then FP25K expression would be restored when target protein expression is desired. This would significantly lower costs for large-scale production of baculovirus-expressed proteins because high titer BV stocks would be easier to produce and the occurrence of deleterious mutations would be reduced. ParaTechs will pursue two complementary approaches to achieve this goal. One involves the production of a virus with an inducible fp25k gene that can be turned off during amplification and activated during target protein expression. The other approach utilizes a virus with a deletion in fp25k coupled with a cell line that expresses FP25K. Each of these approaches has advantages and disadvantages, both in the design phase and for the end user. Experiments described in this proposal will determine which provides higher levels of BVproduction, polyhedrin-linked expression, and stable genome maintenance. Ultimately, the system developed here would be combined with ParaTechs vankyrin expression technology, which increases polyhedrin-driven expression in BEVS from 2- to 20-fold.PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: The baculovirus expression vector system (BEVS) is commonly utilized to produce thousands of proteins for use as vaccines, therapeutics, and for structure-function studies. Unfortunately many researchersare not aware that certain mutations rapidly accumulate leading to lower levels of target gene expression. ParaTechs has developed a strategy to prevent these mutations, while simultaneously providing higher levels of virus production, stable genome maintenance, and target gene expression.

* information listed above is at the time of submission.

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