SBIR-STTR Award

Low-Cost Production of Rapoa-Im for the Treatment of Cardiovascular Disease
Award last edited on: 10/30/14

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$260,890
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Ning Huang

Company Information

Ventria Bioscience (AKA: Applied Phytologics Inc)

12635 East Montview Boulevard
Aurora, CO 80045
   (800) 916-8311
   info@ventria.com
   www.ventria.com
Location: Single
Congr. District: 06
County: Adams

Phase I

Contract Number: 1R43HL120349-01A1
Start Date: 4/15/14    Completed: 3/31/15
Phase I year
2014
Phase I Amount
$260,890
Vascular diseases such as athersclerosis are the major causes of morbidity and mortality worldwide. The high density lipoprotein (HDL) particle is thought to protect the arteries from atherosclerosis by removing excess cholesterol and other lipids from the vessel wall and delivering them to the liver for elimination. The key protein component of HDL is apolipoprotein A-I (ApoA-I). A naturally occurring genetic variant, named ApoA-I Milano (ApoA-IM) is highly potent in reducing atherosclerotic vascular disease. This specific function of ApoA-IM and the HDL particle has become an important therapeutic focus in the HDL-based therapies. However, production of ApoA-IM is extremely difficult and costly thus limiting its therapeutic potential. Ventria Bioscience has developed a plant-based protein expression system in rice grain that produces recombinant protein generally 25 to 1000 fold higher than other plant-based protein expression systems. We hypothesize that we can use this technology to produce functional ApoA-IM in large scale and at low cost. There are four aims in present proposal: 1. production of transgenic rice plants with three different constructs for expressing ApoA-IM in rice grain to achieve a high level expression of recombinant ApoA-IM (rApoA-IM); 2. Expression analysis of transgenic rice seeds and purification of rApoA-IM from transgenic rice seeds; 3. Biochemical analysis of rApoA-IM derived from rice grain and comparison of rice-derived rApoA-IM to that derived from E. coli prepared by our collaborator, The Medicines Company; and 4. Functional analysis of rApoA-IM derived from rice grain and comparison of rice-derived rApoA-IM to that derived from E. coli prepared by our collaborator, The Medicines Company. Rice-derived rApoA-IM will be first tested for its ability to form complex with lipid. Then the complex will be tested in a cell-based assay designed to measure the level of Reverse Cholesterol Efflux which is the mechanism of action of complex developed by The Medicines Company. Based on our past experience, we expect that we will be able to achieve our goals within the proposed time- frame.

Thesaurus Terms:
Animal Model;Apolipoprotein A-I;Apolipoprotein A-I Milano;Apolipoproteins A;Arteries;Atherosclerosis;Base;Biochemical;Biological Assay;Cardiovascular Diseases;Cells;Cereals;Cholesterol;Complex;Coronary Heart Disease;Cost;Design;Development;Effectiveness;Escherichia Coli;Experience;Feasibility Studies;Funding;Genetic Variant;Goals;High Density Lipoprotein Cholesterol;High Density Lipoproteins;In Vitro;In Vivo;Life;Lipids;Liver;Measures;Medicine;Morbidity - Disease Rate;Mortality Vital Statistics;Names;Particle;Phase;Plants;Process;Production;Protein Expression;Proteins;Public Health Relevance;Recombinant Proteins;Recombinants;Request For Proposals;Research Clinical Testing;Reverse Cholesterol Transport;Rice;Risk Factors;Safety Study;Scale Up;Seeds;Small Business Innovation Research Grant;System;Technology;Testing;Therapeutic;Time;Toxicology;Transgenic Organisms;Transgenic Plants;Vascular Diseases;

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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