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Grant: Project Grant

University of Toronto

$944,775.00

Developing phage tail-derived nanomachines as strain specific antibacterial agents

EF 2016-17

Résumé
Bacteriophages (phages) are viruses that infect and kill bacterial strains with a high degree of specificity. Ninety five percent of phages on earth utilize a structure known as a tail to bind to the surface of bacteria for the initiation of infection. Tails impart host specificity to phages by binding proteins or sugars on the cell surface, which are the most variable components of bacteria. This proposal is focused on studying and engineering bacterial-killing nanomachines, called tailocins, which are derived from phage tails. Tailocins are naturally produced by bacteria to use as weapons to kill other bacteria sharing the same environment. They look and act like small harpoons, with the bacterial host specificity encoded at one end. When a tailocin encounters a susceptible bacterial cell, it binds to the surface, pokes a hole in the membrane, and kills the cell. The goal of our research is to understand how tailocins kill bacterial cells and develop robust methods to tailor their killing specificity. In the long term, these studies are aimed at producing agents that may be used as novel alternatives to antibiotics or for precise manipulation of the human microbiome.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
358137
Name
Davidson Alan R
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Developing phage tail-derived nanomachines as strain specific antibacterial agents
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$944,775
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Anti-Bacterial Agents; Bacteriology; Bacteriophage; Pathogenic Bacteria; Phage Tails; Structural Biology
Abstract
Bacteriophages (phages) are viruses that infect and kill bacterial strains with a high degree of specificity. Ninety five percent of phages on earth utilize a structure known as a tail to bind to the surface of bacteria for the initiation of infection. Tails impart host specificity to phages by binding proteins or sugars on the cell surface, which are the most variable components of bacteria. This proposal is focused on studying and engineering bacterial-killing nanomachines, called tailocins, which are derived from phage tails. Tailocins are naturally produced by bacteria to use as weapons to kill other bacteria sharing the same environment. They look and act like small harpoons, with the bacterial host specificity encoded at one end. When a tailocin encounters a susceptible bacterial cell, it binds to the surface, pokes a hole in the membrane, and kills the cell. The goal of our research is to understand how tailocins kill bacterial cells and develop robust methods to tailor their killing specificity. In the long term, these studies are aimed at producing agents that may be used as novel alternatives to antibiotics or for precise manipulation of the human microbiome.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Davidson, Alan R
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $944,775~ $0~