Amplification of Custom RNA in Plants
Amplification of Custom RNA in Plants
批准号:
6525477
负责人:
SERGEI A KAZAKOV
金额:
$57.11万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-08-01 至 2004-08-31
关键词:
RNA autoradiography biotechnology biotherapeutic agent hepatitis C virus high throughput technology method development nucleic acid biosynthesis nucleic acid hybridization nucleic acid purification nucleic acid quantitation /detection nucleic acid structure plants polymerase chain reaction radiotracer ribozymes tobacco mosaic virus transfection /expression vector virus genetics virus protein virus replication
中文摘要
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英文摘要
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.
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