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Grant: Operating Grant

Université de Montréal

$909,850.00

Dynamic interactions of the type IV secretion system assembly factor VirB8

EF 2011-12

Résumé
All pathogenic bacteria need weapons to defend themselves against the immune system in order to thrive in the human body. Among those weapons the secretion systems are especially important since they transfer toxins and other virulence factors into human cells. We study a special secretion system from pathogenic bacteria, the type IV secretion system, which erects structures on the surface of bacteria that engage in toxin transfer into the host. In the absence of the secretion system, the bacteria do not cause disease, because they can not defend themselves against the immune system. The aim of this project is to analyze and understand the molecular details of the interactions of the type IV secretion system component VirB8, which is an Achilles heel of the secretion system. Once we understand these interactions we will be able to block the function of VirB8 and thereby block the secretion system and bacterial pathogenicity. This approach could lead to the development of novel anti-microbial drugs against bacterial pathogens and in our preliminary work we have already identified interesting candidate molecules.
Programme
Operating Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
253981
Name
Baron Christian
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - A
Projecttitle
Dynamic interactions of the type IV secretion system assembly factor VirB8
Programtype2
Operating Grants
Orgnameinp2
Université de Montréal
Cihramount2
$909,850
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Bacterial Virulence; Biochemistry; Medicinal Chemistry; Molecular Docking; Novel Alternative To Antibiotics; Protein-Protein Interactions; Secretion Systems; Small-Molecule Inhibitors; Structural Biology; Structure-Activity Relationship Program
Abstract
All pathogenic bacteria need weapons to defend themselves against the immune system in order to thrive in the human body. Among those weapons the secretion systems are especially important since they transfer toxins and other virulence factors into human cells. We study a special secretion system from pathogenic bacteria, the type IV secretion system, which erects structures on the surface of bacteria that engage in toxin transfer into the host. In the absence of the secretion system, the bacteria do not cause disease, because they can not defend themselves against the immune system. The aim of this project is to analyze and understand the molecular details of the interactions of the type IV secretion system component VirB8, which is an Achilles heel of the secretion system. Once we understand these interactions we will be able to block the function of VirB8 and thereby block the secretion system and bacterial pathogenicity. This approach could lead to the development of novel anti-microbial drugs against bacterial pathogens and in our preliminary work we have already identified interesting candidate molecules.
Competitiondate
201203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Baron, Christian
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $909,850~ $0~