SBIR/STTR Research Award

Amplification of Custom RNA in Plants

Award identifier e8f7d2d07ee0a6c7626b38e87e7d7d2515051d53e905f1d788707091157b2506Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$516,509

Program and phase

SBIR · Phase II

Award year

2001

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Somagenics, Inc.
Proposal award date
Not reported
Contract end date
Not reported
UEI
NWMCAECH9RX7
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): RNA-based technologies have become increasingly prominent in research and biotechnology since the discovery of catalytic RNA (ribozymes), techniques for selection of novel functions from random libraries of RNA, and the widespread use of microarrays. However, the cost of producing RNA by synthetic or enzymatic means remains high-at least ten times the cost of DNA, and synthetic methods are limited to short RNAs. This proposal describes a novel method for the low-cost, largescale production of custom RNA products of any length based on amplification in plants using viral vectors, an approach that has been successfully used for the production of protein products. After infection with recombinant virus, the plants are harvested, virions are isolated using an established, single-step procedure, RNA is extracted, and the desired fragment is excised and purified in a simple procedure. Yields of viral RNA are approximately 0.5 percent of total dry plant mass. In Phase I of this project we established proof of principle by demonstrating the insertion of a custom RNA fragment into the viral RNA vector, which remained completely stable and intact under normal storage and in vivo conditions. Upon addition of a new solution component, the insert was efficiently excised from the vector. In Phase II, we will develop this approach into a practical method ready for commercialization. This will involve a series of optimizations to make the system robust enough to overcome any obstacles that may emerge for certain custom RNAs. Our first demonstration of large-scale RNA production from plants will be to several hundred milligrams of a candidate therapeutic ribozyme and a key element of the hepatitis C virus. PROPOSED COMMERCIAL APPLICATION: RNA is an important target for structural biology and biomedical studied including HIV and influenza viruses. It also has potential in antisense and ribozyme therapeutics, biotechnology products and molecular biology tools: Our technology would provide large amounts of custom RNAs less expensively and more efficiently than alternative methods. Our current business strategy is to sell custom RNA in partnership with Large Scale Biology Corp. and license the technology to certain other manufacturers.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Research funding history

39 SBIR/STTR records share this UEI (1994–2020). Reported award amounts total $23,258,381. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.