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Grant: Project Grant

University of Toronto

$1,201,050.00

Using Herpesvirus Proteomics to Identify Mechanisms of Cellular Regulation

FY 2016-17

Summary
Most people are infected with three different herpesviruses; herpes simplex virus type 1 (HSV-1), cytomegalovirus (CMV) and Epstein-Barr virus (EBV). These life-long infections can be asymptomatic or can lead to a variety of health problems including oral lesions, mononucleosis, cancer and life-threatening illnesses in immune suppression. These viruses persist and cause disease through the action of the numerous proteins that they encode, which bind to and manipulate the functions of some cellular proteins. However the functions and cellular targets of most of the viral proteins have not yet been determined. This project uses comprehensive protein interaction methods and a unique library of HSV-1, EBV and CMV proteins to determine the cellular targets of the viral proteins. We are particularly interested in cellular proteins that are targeted by all three viruses as this would reflect the importance of these cellular proteins for viral infection and cellular regulation in general. This work will provide insight into how viruses manipulate cells to cause disease and enable life-long persistence, and will identify potential drug targets for antiviral treatments. It will also identify new mechanisms of regulating important cellular processes.
Program
Project Grant
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
356847
Name
Frappier Lori D
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Using Herpesvirus Proteomics to Identify Mechanisms of Cellular Regulation
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$1,201,050
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Affinity Purification-Mass Spectroscopy; Cytomegalovirus; Epstein-Barr Virus; Herpes Simplex Virus; Protein Interactions
Abstract
Most people are infected with three different herpesviruses; herpes simplex virus type 1 (HSV-1), cytomegalovirus (CMV) and Epstein-Barr virus (EBV). These life-long infections can be asymptomatic or can lead to a variety of health problems including oral lesions, mononucleosis, cancer and life-threatening illnesses in immune suppression. These viruses persist and cause disease through the action of the numerous proteins that they encode, which bind to and manipulate the functions of some cellular proteins. However the functions and cellular targets of most of the viral proteins have not yet been determined. This project uses comprehensive protein interaction methods and a unique library of HSV-1, EBV and CMV proteins to determine the cellular targets of the viral proteins. We are particularly interested in cellular proteins that are targeted by all three viruses as this would reflect the importance of these cellular proteins for viral infection and cellular regulation in general. This work will provide insight into how viruses manipulate cells to cause disease and enable life-long persistence, and will identify potential drug targets for antiviral treatments. It will also identify new mechanisms of regulating important cellular processes.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Frappier, Lori D
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,201,050~ $0~
University of Toronto - $1,201,050 Grant (2016-17) | Canada Spends