Grant: Engage Grants Program
University of Ontario Institute of Technology
$25,000.00
Development of a novel technology for in vitro evaluation of RNA/DNA-targeted compounds
FY 2017-18
Summary
The high adaptation ability of bacteria to existing antibacterial agents is a major issue that requires newapproaches in the design of novel antibiotics. One such approach, used by a small hi-tech Canadian companyOtava Ltd, is based on selective binding of chemical molecules to specific bacterial RNA or DNA sequences.This binding leads to depletion of bacteria growth and reproduction. Here we propose a new methodology forchemical screening and evaluation of compounds designed to selectively bind microbial RNA/DNA. Usingcomputer simulation methods, Otava Inc. has created novel libraries of fine organic compounds that matchphysical and structural parameters of typical RNA/DNA targets. Further screening steps aimed to determinethe most promising pre-antibiotics are very expensive, time-consuming, and require special biohazardaccredited laboratory facilities. For now, Otava Inc. needs to collaborate with large pharmaceutical companiesto perform in vivo screening of the activity of each compound they produce. This approach significantlyincreases the turnover time between the development of the product and commercialization of the findings. Thelack of the fast screening method to evaluate the activity of their compounds is hampering their researchabilities and limiting their ability to grow. We believe that we will be able to develop a purely chemical methodto estimate the potential of organic compounds from the library to act as selective inhibitors of duplication ofspecific bacterial DNA sequences. This will allow eliminating less effective compounds and proposing highquality competitive commercial products to the pharmaceutical industry. We expect this to allow the smallOntario company to grow and compete with larger international companies. It is not a secret that it is verydifficult for Canadian companies to compete with third-world countries that over-use cheap labor power andmaintain poor working environments to reduce the cost of their products. We want to use our scientificstrengths to optimize the process of pharmaceutical screening and allow Canadian companies to intensify theirresearch power while maintaining high standards of work environment and living.
Program
Engage Grants Program
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
514863-2017
Name nom
Zenkina, Olena
Department département
Science, Faculty of
Organization id
19222
Institution établissement
University of Ontario Institute of Technology
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2017
Award amount
25000
Program id
EGP
Program name en
Engage Grants Program
Program name fr
Programme de subventions d'engagement partenariat
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
1553
Committee name en
Ontario Internal Decision Committee
Committee name fr
Comité de décision interne pour l'Ontario
Area of application code
400
Area of application group en
Environment
Area of application group fr
Environnement
Area of application en
Environment
Area of application fr
Environnement
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
Development of a novel technology for in vitro evaluation of RNA/DNA-targeted compounds
Keyword
NSERC
Application summary
The high adaptation ability of bacteria to existing antibacterial agents is a major issue that requires newapproaches in the design of novel antibiotics. One such approach, used by a small hi-tech Canadian companyOtava Ltd, is based on selective binding of chemical molecules to specific bacterial RNA or DNA sequences.This binding leads to depletion of bacteria growth and reproduction. Here we propose a new methodology forchemical screening and evaluation of compounds designed to selectively bind microbial RNA/DNA. Usingcomputer simulation methods, Otava Inc. has created novel libraries of fine organic compounds that matchphysical and structural parameters of typical RNA/DNA targets. Further screening steps aimed to determinethe most promising pre-antibiotics are very expensive, time-consuming, and require special biohazardaccredited laboratory facilities. For now, Otava Inc. needs to collaborate with large pharmaceutical companiesto perform in vivo screening of the activity of each compound they produce. This approach significantlyincreases the turnover time between the development of the product and commercialization of the findings. Thelack of the fast screening method to evaluate the activity of their compounds is hampering their researchabilities and limiting their ability to grow. We believe that we will be able to develop a purely chemical methodto estimate the potential of organic compounds from the library to act as selective inhibitors of duplication ofspecific bacterial DNA sequences. This will allow eliminating less effective compounds and proposing highquality competitive commercial products to the pharmaceutical industry. We expect this to allow the smallOntario company to grow and compete with larger international companies. It is not a secret that it is verydifficult for Canadian companies to compete with third-world countries that over-use cheap labor power andmaintain poor working environments to reduce the cost of their products. We want to use our scientificstrengths to optimize the process of pharmaceutical screening and allow Canadian companies to intensify theirresearch power while maintaining high standards of work environment and living.