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Grant: Operating Grant

University of British Columbia

$623,580.00

Metallo-beta-lactamases; mechanistic and evolutionary studies for broad specificity and inhibitor binding.

EF 2012-13

Résumé
Pathogenic bacteria, such as P. aeruginosa. E. coli and K. pneumonia, can cause serious infectious diseases such as pneumonia, urinary tract infections, and diarrhea. These bacteria are becoming resistant to many commonly used antibiotics. In addition, the spreading of such pathogenic bacteria that are resistant to multiple antibiotics has become more rapid during the past decade. The resistant bacteria area serious threat to Canadian and global health, and new strategies are needed to combat them. The underlying cause for bacterial resistance is the action of a group of enzymes called beta-lactamases, which destroy beta-lactam antibiotics such as penicillin. Moreover, on-going changes in bacterial beta-lactamase genes in nature are producing more potent enzymes to destroy even our newest antibiotics. This proposal describes research to study the ways that beta-lactamase enzymes change and adapt to antibiotics. We will combine experiments to identify mechanisms of change with detailed studies of enzyme function so that we can develop ways to block their activity. Ultimately, the information obtained in this research program will be used to develop novel, persistent and sustainable antibiotics and inhibitors against pathogenic bacteria.
Programme
Operating Grant
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
266119
Name
Tokuriki Nobuhiko
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - A
Projecttitle
Metallo-beta-lactamases; mechanistic and evolutionary studies for broad specificity and inhibitor binding.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$623,580
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Beta-Lacatamase Inhibitor; Beta-Lactam Antibiotics; Crystallography; Experimental Evolution; Function-Structure Relationship; Metallo-Beta-Lactamase; Mutations; Nmr; Substrate Specificity
Abstract
Pathogenic bacteria, such as P. aeruginosa. E. coli and K. pneumonia, can cause serious infectious diseases such as pneumonia, urinary tract infections, and diarrhea. These bacteria are becoming resistant to many commonly used antibiotics. In addition, the spreading of such pathogenic bacteria that are resistant to multiple antibiotics has become more rapid during the past decade. The resistant bacteria area serious threat to Canadian and global health, and new strategies are needed to combat them. The underlying cause for bacterial resistance is the action of a group of enzymes called beta-lactamases, which destroy beta-lactam antibiotics such as penicillin. Moreover, on-going changes in bacterial beta-lactamase genes in nature are producing more potent enzymes to destroy even our newest antibiotics. This proposal describes research to study the ways that beta-lactamase enzymes change and adapt to antibiotics. We will combine experiments to identify mechanisms of change with detailed studies of enzyme function so that we can develop ways to block their activity. Ultimately, the information obtained in this research program will be used to develop novel, persistent and sustainable antibiotics and inhibitors against pathogenic bacteria.
Competitiondate
201209
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Tokuriki, Nobuhiko
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $623,580~ $0~