Résumé
Two fluorescence probes for the detection of cysteine (Cys), glutathione (GSH) and other biothiols, such as homocysteine (Hcy) and cysteinyl-glycine (Cys-Gly), were developed. These molecular probes are coumarin-based derivatives containing a chalcone-like moiety that reacts with biothiols through a Michael addition reaction, leading to strong fluorescence enhancements. The reactivity of the tested biothiols toward both probes (ChC1 and ChC2) follows the order Cys > GSH > Hcy > Cys-Gly, ChC1 being less reactive than ChC2. Possible interference with other amino acids was assessed. ChC1 and ChC2 display a highly selective fluorescence enhancement with thiols, allowing these probes to be used for fluorimetric thiol determination in SH-SY5Y cells.
Langue d'origine | English |
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Pages (de-à) | 6606-6609 |
Nombre de pages | 4 |
Journal | Tetrahedron Letters |
Volume | 52 |
Numéro de publication | 49 |
DOI | |
Statut de publication | Published - déc. 7 2011 |
Financement
This work was supported by FONDECYT (Grants #11090115 and 1100640 ), and the Millennium Scientific Initiative (Grant P05-001-F ).
Bailleurs de fonds | Numéro du bailleur de fonds |
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Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica | 11090115, P05-001-F, 1100640 |
ASJC Scopus Subject Areas
- Biochemistry
- Drug Discovery
- Organic Chemistry