Grant: Discovery Grants Program - Individual
University of Ontario Institute of Technology
$29,000.00
Synthesis and Applications of Chemically-Modified Oligonucleotides
EF 2019-20
Résumé
Nucleic*acids are the main building blocks of DNA and RNA, which are biomacromolecules*with vast biological function. For example, nucleic acids contain the genetic blue print of the cell, and transfer of this genetic code to messenger RNA is necessary to direct the synthesis of unique proteins. Nucleic acids also have other biological functions including controlling the expression of particular genes. Since the*discovery of the double helical structure of DNA 65 years ago, there have been*significant advances in the nucleic acid field to improve its properties for*biotechnological applications or for modern medicine. For instance, gene-silencing oligonucleotides are tools used to understand gene function. However, limitations continue due to the native structure of these molecules. Using organic chemistry, my research program develops synthetic analogs in order*to improve its biological function. My research group then evaluates the biological impact of these*synthetic analogs. ******The primary focus of my research group involves synthesizing novel*chemically-modified oligonucleotides to use as gene-silencing oligonucleotides.*First, we will explore the effect of expanding small molecules within a class*of gene silencing molecules called short interfering RNAs (siRNAs). My lab has identified an area within siRNAs that is amenable to diverse chemical modification. As such, we will expand the scope and place*molecules that can interact directly with different cellular biological components. When bound, these molecules may exhibit improved potency, cell-membrane permeability, and stability.******Secondly,*we will expand the scope of photoresponsive groups within siRNAs. Our lab has shown that the photoresponsive*molecule, azobenzene, when placed within the core central region of siRNAs can*be used to reversibly control the timing of gene silencing activity. Azobenzene can isomerize between a trans and*cis form in the presence of visible and ultra-violet light, respectively. We will expand the scope of photoresponsive*RNA groups, and explore functionalized azobenzene derivatives within siRNAs. This will allow us to fine-tune the activity*of siRNAs, and allow us to better control its activity, and thus prevent*off-target effects.******Finally, my*research group has expertise in developing novel backbone modifications for*oligonucleotides. We will expand the*scope of these modifications and explore their effect within the CRISPR (clustered regularly interspaced*short palindromic repeats)/Cas9 editing system. The*CRISPR/Cas9 system is an exciting, and relatively new system that has been*shown to be amenable within a variety of biological systems. ******The multidisciplinary*laboratory work is conducted by a talented team of undergraduate and graduate*students who use a combination of solution-phase, solid-phase and biological*techniques. As such, the trainees*supervised from my lab are well prepared for a variety of professions including*careers focused in chemistry and science.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2019-04692
Name nom
Desaulniers, JeanPaul
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
2019
Competition year année de concours
2019
Award amount
29000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
3705
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Bio-organic chemistry
Research subject fr
Chimie bio-organique
Installment
inst:1 - 5
Partie
1
Nb partie
5
Application title
Synthesis and Applications of Chemically-Modified Oligonucleotides
Keyword
NSERC
Application summary
Nucleic*acids are the main building blocks of DNA and RNA, which are biomacromolecules*with vast biological function. For example, nucleic acids contain the genetic blue print of the cell, and transfer of this genetic code to messenger RNA is necessary to direct the synthesis of unique proteins. Nucleic acids also have other biological functions including controlling the expression of particular genes. Since the*discovery of the double helical structure of DNA 65 years ago, there have been*significant advances in the nucleic acid field to improve its properties for*biotechnological applications or for modern medicine. For instance, gene-silencing oligonucleotides are tools used to understand gene function. However, limitations continue due to the native structure of these molecules. Using organic chemistry, my research program develops synthetic analogs in order*to improve its biological function. My research group then evaluates the biological impact of these*synthetic analogs. ******The primary focus of my research group involves synthesizing novel*chemically-modified oligonucleotides to use as gene-silencing oligonucleotides.*First, we will explore the effect of expanding small molecules within a class*of gene silencing molecules called short interfering RNAs (siRNAs). My lab has identified an area within siRNAs that is amenable to diverse chemical modification. As such, we will expand the scope and place*molecules that can interact directly with different cellular biological components. When bound, these molecules may exhibit improved potency, cell-membrane permeability, and stability.******Secondly,*we will expand the scope of photoresponsive groups within siRNAs. Our lab has shown that the photoresponsive*molecule, azobenzene, when placed within the core central region of siRNAs can*be used to reversibly control the timing of gene silencing activity. Azobenzene can isomerize between a trans and*cis form in the presence of visible and ultra-violet light, respectively. We will expand the scope of photoresponsive*RNA groups, and explore functionalized azobenzene derivatives within siRNAs. This will allow us to fine-tune the activity*of siRNAs, and allow us to better control its activity, and thus prevent*off-target effects.******Finally, my*research group has expertise in developing novel backbone modifications for*oligonucleotides. We will expand the*scope of these modifications and explore their effect within the CRISPR (clustered regularly interspaced*short palindromic repeats)/Cas9 editing system. The*CRISPR/Cas9 system is an exciting, and relatively new system that has been*shown to be amenable within a variety of biological systems. ******The multidisciplinary*laboratory work is conducted by a talented team of undergraduate and graduate*students who use a combination of solution-phase, solid-phase and biological*techniques. As such, the trainees*supervised from my lab are well prepared for a variety of professions including*careers focused in chemistry and science.