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Grant: Engage Grants Program

University of Ontario Institute of Technology

$25,000.00

Using a Nanopore with a Central Cavity to Selectively Translocate DNA Strands of a Specified Length

EF 2016-17

Résumé
Separation of DNA strands by size and subsequent isolation of specific fragment size ranges (size selection) isa requisite step for genomic analysis techniques and biotechnology applications that involve DNA. Gelelectrophoresis (GE) is the most common technique for size selection. In GE, the solution containing DNAstrands of different lengths is flowed through a gel via an external electric field. Due to the porosity of the gel,short strands move faster through the gel than long strands. Thus, after some time, strands of different lengthswill be at different locations in the gel. The section containing the desired strands can then be cut out of the geland purified for further analysis. While this approach is inexpensive and reliable, it does suffer somedrawbacks: it is time and labour intensive, prone to variability, and requires a large experimental setup that isindependent of the setup required for the actual genetic analysis. Coastal Genomics develops and sellsautomated solutions for separation by size via gel electrophoresis. This automation addresses the issue of beinglabour intensive and prone to variability, but the other drawbacks remain. Dr. de Haan has developed a novelnanopore design in which there is a large cavity between narrow entrance and exit pores. Simulations of thisgeometry for a generic polymer model demonstrate that this device is able to sort polymers by size - and it canin fact be tuned to have chains of an intermediate length pass through the device quickest with both shorter andlonger strands lagging behind. As opposed to GE, this technology is intrinsically automated, shows potential tobe time efficient and effective for a wide range of DNA sizes, and could be directly integrated into a largernano/micro-fluidic device in which the device is an in-line precursor to further downstreamanalysis/modification. This technology thus shows potential as a disruptive development for DNA sorting forgenomic and biotechnology applications and thus is of great interest for Coastal Genomics. The goal of thisgrant is to perform detailed simulations that reflect applications of interest to Coastal Genomics as a practicaltest of the technology to inform decisions for further development.
Programme
Engage Grants Program
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
506796-2016
Name nom
DeHaan, Hendrick
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
2016
Competition year année de concours
2016
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
1102
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Biomedical engineering
Area of application fr
Génie biomédical
Research subject code
3113
Research subject group en
Physics
Research subject group fr
Physique
Research subject en
Biophysics
Research subject fr
Biophysique
Partie
1
Nb partie
1
Application title
Using a Nanopore with a Central Cavity to Selectively Translocate DNA Strands of a Specified Length
Keyword
NSERC
Application summary
Separation of DNA strands by size and subsequent isolation of specific fragment size ranges (size selection) isa requisite step for genomic analysis techniques and biotechnology applications that involve DNA. Gelelectrophoresis (GE) is the most common technique for size selection. In GE, the solution containing DNAstrands of different lengths is flowed through a gel via an external electric field. Due to the porosity of the gel,short strands move faster through the gel than long strands. Thus, after some time, strands of different lengthswill be at different locations in the gel. The section containing the desired strands can then be cut out of the geland purified for further analysis. While this approach is inexpensive and reliable, it does suffer somedrawbacks: it is time and labour intensive, prone to variability, and requires a large experimental setup that isindependent of the setup required for the actual genetic analysis. Coastal Genomics develops and sellsautomated solutions for separation by size via gel electrophoresis. This automation addresses the issue of beinglabour intensive and prone to variability, but the other drawbacks remain. Dr. de Haan has developed a novelnanopore design in which there is a large cavity between narrow entrance and exit pores. Simulations of thisgeometry for a generic polymer model demonstrate that this device is able to sort polymers by size - and it canin fact be tuned to have chains of an intermediate length pass through the device quickest with both shorter andlonger strands lagging behind. As opposed to GE, this technology is intrinsically automated, shows potential tobe time efficient and effective for a wide range of DNA sizes, and could be directly integrated into a largernano/micro-fluidic device in which the device is an in-line precursor to further downstreamanalysis/modification. This technology thus shows potential as a disruptive development for DNA sorting forgenomic and biotechnology applications and thus is of great interest for Coastal Genomics. The goal of thisgrant is to perform detailed simulations that reflect applications of interest to Coastal Genomics as a practicaltest of the technology to inform decisions for further development.