Grant: Idea to Innovation
University of Ottawa
$122,000.00
Aptamer-mediated purification for viruses
FY 2013-14
Summary
My research group recently developed Switchable Aptamers (SwAps), single-stranded DNA oligonucleotides, of controlled affinity and selectivity toward oncolytic viruses that can allow the release of the intact virus upon treatment with a simple universal eluting agent. This new technology has the potential to revolutionize affinity-based purification and separation. Using this method, we were able to obtain an ultrapure vesicular stomatitis virus, VSV, which is particularly effective against metastatic cancers that are difficult to treat via conventional therapy. There is no other method for VSV purification that approaches the efficiency and simplicity of our SwAp-based purification technique. Early laboratory studies have conclusively shown that the developed SwAps can efficiently capture VSV in the presence of Ca and Mg ions and also release the captured virus using an eluting solution with chelating agents such as EDTA and EGTA. We are now at a stage where the SwAps technology is ready to move to the reduction-to-practice stage. The overall goals for Phase 1 of this I2I proposal are to develop our SwAp-based purification technique into a robust and easily manufactured platform technology by achieving the following steps: 1) Enhancement of the target biomolecule capture and recovery; 2) Improvement of the SwAps stability during frequent purification cycles; 3) Investigation of economic and efficient chromatographic matrices; 4) Optimization of the purification process; 5) Third party evaluation and validation. Achievement of these goals will result in the development of a robust technology that will meet the key needs of customers involved in purification of biomolecules of pharmaceutical and medicinal significance and will form the basis for both a start-up company and a product line that can be deployed in short period.
Program
Idea to Innovation
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
451915-2013
Name nom
Berezovski, Maxim
Department département
Chemistry
Organization id
28
Institution établissement
University of Ottawa
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2013
Award amount
122000
Program id
I2IPJ
Program name en
Idea to Innovation
Program name fr
De l'idée à l'innovation
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
500
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Manufacturing processes and products
Area of application fr
Procédés et produits industriels
Research subject code
3504
Research subject group en
Analytical chemistry
Research subject group fr
Chimie analytique
Research subject en
Bioanalytical chemistry
Research subject fr
Chimie bioanalytique
Partie
1
Nb partie
1
Application title
Aptamer-mediated purification for viruses
Keyword
NSERC
Application summary
My research group recently developed Switchable Aptamers (SwAps), single-stranded DNA oligonucleotides, of controlled affinity and selectivity toward oncolytic viruses that can allow the release of the intact virus upon treatment with a simple universal eluting agent. This new technology has the potential to revolutionize affinity-based purification and separation. Using this method, we were able to obtain an ultrapure vesicular stomatitis virus, VSV, which is particularly effective against metastatic cancers that are difficult to treat via conventional therapy. There is no other method for VSV purification that approaches the efficiency and simplicity of our SwAp-based purification technique. Early laboratory studies have conclusively shown that the developed SwAps can efficiently capture VSV in the presence of Ca and Mg ions and also release the captured virus using an eluting solution with chelating agents such as EDTA and EGTA. We are now at a stage where the SwAps technology is ready to move to the reduction-to-practice stage. The overall goals for Phase 1 of this I2I proposal are to develop our SwAp-based purification technique into a robust and easily manufactured platform technology by achieving the following steps: 1) Enhancement of the target biomolecule capture and recovery; 2) Improvement of the SwAps stability during frequent purification cycles; 3) Investigation of economic and efficient chromatographic matrices; 4) Optimization of the purification process; 5) Third party evaluation and validation. Achievement of these goals will result in the development of a robust technology that will meet the key needs of customers involved in purification of biomolecules of pharmaceutical and medicinal significance and will form the basis for both a start-up company and a product line that can be deployed in short period.