The development of a fluorescence turn-on sensor for cysteine, glutathione and other biothiols. A kinetic study

Olimpo García-Beltrán, Natalia Mena, Edwin G. Pérez, Bruce K. Cassels, Marco T. Nuñez, Francisca Werlinger, Daniel Zavala, Margarita E. Aliaga, Paulina Pavez

Producción científicarevisión exhaustiva

30 Citas (Scopus)

Resumen

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.

Idioma originalEnglish
Páginas (desde-hasta)6606-6609
Número de páginas4
PublicaciónTetrahedron Letters
Volumen52
N.º49
DOI
EstadoPublished - dic. 7 2011

Financiación

This work was supported by FONDECYT (Grants #11090115 and 1100640 ), and the Millennium Scientific Initiative (Grant P05-001-F ).

FinanciadoresNúmero del financiador
Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica11090115, P05-001-F, 1100640

    ASJC Scopus Subject Areas

    • Biochemistry
    • Drug Discovery
    • Organic Chemistry

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