| Literature DB >> 16759107 |
M Eugenio Vázquez1, Juan B Blanco, Severo Salvadori, Claudio Trapella, Roberto Argazzi, Sharon D Bryant, Yunden Jinsmaa, Lawrence H Lazarus, Lucia Negri, Elisa Giannini, Roberta Lattanzi, Mariantonella Colucci, Gianfranco Balboni.
Abstract
A new environment-sensitive fluorophore, 6-N,N-(dimethylamino)-2,3-naphthalimide (6DMN) was introduced in the delta-selective opioid peptide agonist H-Dmt-Tic-Glu-NH(2) and in the mu-selective opioid peptide agonist endomorphin-2 (H-Tyr-Pro-Phe-Phe-NH(2)). Environment-sensitive fluorophores are a special class of chromophores that generally exhibit a low quantum yield in aqueous solution but become highly fluorescent in nonpolar solvents or when bound to hydrophobic sites in proteins or membranes. New fluorescent delta-selective irreversible antagonists (H-Dmt-Tic-Glu-NH-(CH(2))(5)-CO-Dap(6DMN)-NH(2) (1) and H-Dmt-Tic-Glu-Dap(6DMN)-NH(2) (2)) were identified as potential fluorescent probes showing good properties for use in studies of distribution and internalization of delta receptors by confocal laser scanning microscopy.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16759107 PMCID: PMC1994907 DOI: 10.1021/jm060343t
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446