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Grant: Discovery Grants Program - Individual

University of Manitoba

$68,000.00

Investigation of viral ribonucleic acid recognition by human innate immune enzymes

FY 2022-23

Summary
A hallmark of many viral infections is the production of foreign nucleic acid molecules that are generated during the life cycle of the virus. Host cells respond to these foreign biomolecules through a variety of mechanisms, including the use of nucleic acid sensor proteins that detect and mount a defensive response against the infection. My laboratory will focus investigation on two important families of nucleic-acid binding proteins that are central to the recognition of viral infection: (i) 2'-5' oligoadenylate synthetases (OAS) and (ii) the RNA-dependent protein kinase (PKR). The interaction between these enzymes and foreign nucleic acid molecules helps to prevent viral replication by blocking necessary viral protein production. My laboratory will continue a research program to characterize the interactions between naturally occurring viral nucleic acid molecules and OAS/PKR enzymes to provide a fundamental understanding of a key mechanism used by host cells to respond to viral invasion. Biochemical characterization will identify key features of viral nucleic acid molecules, and structural biology approaches will generate three-dimensional images of complexes of interest. A novel aspect of the proposed research program is the use of naturally occurring viral nucleic acid molecules as the model systems as most studies to date have employed synthetic nucleic acid molecules that lack key characteristics typical of their viral counterparts. The results expected from the proposed research program will therefore contribute to our understanding of how these enzymes distinguish between viral and host-cell nucleic acid molecules. Trainees in my laboratory have and will continue to benefit from our expertise in the investigation of protein-nucleic acid interactions and acquire an in-demand skill set given the emerging importance of these interactions in a wide variety of biologically important systems. Highly qualified personnel trained will be well equipped for careers in basic scientific research focused on biotechnology, molecular biology, biochemistry, structural biology, and proteomics.
Program
Discovery Grants Program - Individual
Location
Manitoba, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
RGPIN-2015-06142
Name nom
McKenna, Sean
Department département
Chemistry - Chemistry
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2022
Competition year année de concours
2015
Award amount
68000
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
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
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
5400
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Biochemistry
Research subject fr
Biochimie
Installment
inst:8;9
Partie
2
Nb partie
9
Application title
Investigation of viral ribonucleic acid recognition by human innate immune enzymes
Application summary
A hallmark of many viral infections is the production of foreign nucleic acid molecules that are generated during the life cycle of the virus. Host cells respond to these foreign biomolecules through a variety of mechanisms, including the use of nucleic acid sensor proteins that detect and mount a defensive response against the infection. My laboratory will focus investigation on two important families of nucleic-acid binding proteins that are central to the recognition of viral infection: (i) 2'-5' oligoadenylate synthetases (OAS) and (ii) the RNA-dependent protein kinase (PKR). The interaction between these enzymes and foreign nucleic acid molecules helps to prevent viral replication by blocking necessary viral protein production. My laboratory will continue a research program to characterize the interactions between naturally occurring viral nucleic acid molecules and OAS/PKR enzymes to provide a fundamental understanding of a key mechanism used by host cells to respond to viral invasion. Biochemical characterization will identify key features of viral nucleic acid molecules, and structural biology approaches will generate three-dimensional images of complexes of interest. A novel aspect of the proposed research program is the use of naturally occurring viral nucleic acid molecules as the model systems as most studies to date have employed synthetic nucleic acid molecules that lack key characteristics typical of their viral counterparts. The results expected from the proposed research program will therefore contribute to our understanding of how these enzymes distinguish between viral and host-cell nucleic acid molecules. Trainees in my laboratory have and will continue to benefit from our expertise in the investigation of protein-nucleic acid interactions and acquire an in-demand skill set given the emerging importance of these interactions in a wide variety of biologically important systems. Highly qualified personnel trained will be well equipped for careers in basic scientific research focused on biotechnology, molecular biology, biochemistry, structural biology, and proteomics.