Grant: Travel Awards - Institute Community Support
Direct Payment
$1,000.00
Development of Caged Angiotensin-II Analogs: New Photo Releasable Probes to Study Intracrine Pharmacology in Cardiac Cells
EF 2013-14
Résumé
Angiotensin receptors are present within the body, more abundantly in the heart, kidney, lung, brain and mediate key physiological responses. At the cellular level, these receptors are present on the surface and intracellularly. The specific biological responses and mechanisms of intracellular receptors are less known because of difficulty in selectively targeting the intracrine system. Chemical synthesis of peptides offers the possibility to incorporate residues, like a photo-cleavable moiety, into amino acid sequences. In the present study we present a new caged analog [Tyr(DMNB)4]Ang-II that provides a temporally and spatially controlled release of Ang-II upon UV-irradiation and provides a versatile tool for studying the function and molecular pharmacology of intracrine Ang-II signalling.
Programme
Travel Awards - Institute Community Support
Bénéficiaire
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
303757
Name
Tadevosyan Artavazd
Region
Québec
Country
Canada
Orgtype
Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Institute of Circulatory and Respiratory Health
Projecttitle
Development of Caged Angiotensin-II Analogs: New Photo Releasable Probes to Study Intracrine Pharmacology in Cardiac Cells
Programtype2
Undefined
Orgnameinp2
Direct Payment
Cihramount2
$1,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Caged Peptide; Calcium; Cardiomyocyte; Intracrine Ras; Photosensitive Angiotensin Ii
Abstract
Angiotensin receptors are present within the body, more abundantly in the heart, kidney, lung, brain and mediate key physiological responses. At the cellular level, these receptors are present on the surface and intracellularly. The specific biological responses and mechanisms of intracellular receptors are less known because of difficulty in selectively targeting the intracrine system. Chemical synthesis of peptides offers the possibility to incorporate residues, like a photo-cleavable moiety, into amino acid sequences. In the present study we present a new caged analog [Tyr(DMNB)4]Ang-II that provides a temporally and spatially controlled release of Ang-II upon UV-irradiation and provides a versatile tool for studying the function and molecular pharmacology of intracrine Ang-II signalling.
Competitiondate
201401
Approvedterm2
0 yr 3 mths
Pinamesdelim
Tadevosyan, Artavazd
Approvedterm
0 an 3 mois
Cihrcontribution2
Inst of Circ &Respiratory Hlth~ $1,000~ $0~