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Grant: Operating Grant

Université de Montréal

$515,249.00

Dissecting 7 transmembrane receptor's pathways through designed separation of function.

EF 2009-10

Résumé
Seven transmembrane receptors (7TMR) represent the largest class of therapeutic targets for the development of new drugs in a vast diversity of clinical indications. Although these receptors have been the object of intense research for the last 30 years or so, our understanding of how drugs can target these receptors to have specific therapeutic activities remains very incomplete. Results obtained in the last few years by our group and others have open new avenues toward a better understanding of the mechanisms underlying the selectivity of drug actions through 7TMR. Recent advances in bioinformatic and phylogenomic analysis offers new means to explore these avenues with the hope of developing new drugs with better therapeutic profiles. The present grant application proposes to combine the use of such new bioinformatic analytical tools with molecular and cellular biology methods in order to unravel the molecular determinants of drug action selectivity.
Programme
Operating Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
190913
Name
Bouvier Michel
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Pharmacology & Toxicology
Projecttitle
Dissecting 7 transmembrane receptor's pathways through designed separation of function.
Programtype2
Operating Grants
Orgnameinp2
Université de Montréal
Cihramount2
$515,249
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Beta-Arrestin; Cell Signalling; Evolutionary Trace Analysis; Functional Selectivity; G Proteins; Seven Transmembrane Receptors
Abstract
Seven transmembrane receptors (7TMR) represent the largest class of therapeutic targets for the development of new drugs in a vast diversity of clinical indications. Although these receptors have been the object of intense research for the last 30 years or so, our understanding of how drugs can target these receptors to have specific therapeutic activities remains very incomplete. Results obtained in the last few years by our group and others have open new avenues toward a better understanding of the mechanisms underlying the selectivity of drug actions through 7TMR. Recent advances in bioinformatic and phylogenomic analysis offers new means to explore these avenues with the hope of developing new drugs with better therapeutic profiles. The present grant application proposes to combine the use of such new bioinformatic analytical tools with molecular and cellular biology methods in order to unravel the molecular determinants of drug action selectivity.
Competitiondate
200909
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Bouvier, Michel
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $515,249~ $0~