A fluorescent probe for biothiols based on the conjugate addition of thiols to α,β-unsaturated ester

✍ Scribed by Jun Du; Zhe Yang; Haiping Qi; Xiao-Feng Yang

• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 698 KB
• Volume: 26
• Category: Article
• ISSN: 1522-7235
• DOI: 10.1002/bio.1257

✦ Synopsis

ABSTRACT

A sensitive fluorogenic probe 1 for biothiols was developed based on the Michael addition reaction. The probe 1 was readily synthesized via the reaction of 2‐(4′‐hydroxyphenyl) benzimidazole (HPBI) with acryloyl chloride and shows weak fluorescence emission. Upon mixing with biothiols, the fluorescence of 1 is significantly enhanced due to the conjugate addition of thiols to the α,β‐unsaturated carbonyl moiety, thus eliminating the photoinduced electron transfer (PET) quenching of the fluorophore by the intramolecular carbon–carbon double bond. Cysteine (Cys) was selected as the representative thiol in the spectral experiment. A good linear relationship was obtained from 1.0 to 30.0 µmol L^−1^ for Cys and the detection limit was 0.17 µmol L^−1^. Furthermore, probe 1 was highly selective for biothiols without the interference of some biologically relevant analytes and has been applied to detecting biothiols in human urine samples. Copyright © 2010 John Wiley & Sons, Ltd.