Electrochemical latent redox ratiometric probes for real-time tracking and quantification of endogenous hydrogen sulfide production in living cells

被引:61
作者
Manibalan, Kesavan [1 ]
Mani, Veerappan [1 ]
Chang, Pu-Chieh [1 ,2 ]
Huang, Chih-Hung [1 ,2 ]
Huang, Sheng-Tung [1 ,2 ]
Marchlewicz, Kasper [1 ,3 ]
Neethirajan, Suresh [4 ]
机构
[1] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei 10608, Taiwan
[2] Natl Taipei Univ Technol, Inst Biochem & Biomed Engn, Taipei 10608, Taiwan
[3] Warsaw Univ Technol, Fac Chem, Warsaw, Poland
[4] Univ Guelph, BioNano Lab, Sch Engn, Guelph, ON N1G5 2W1, Canada
关键词
Hydrogen sulfide; Gasotransmitter; Real-time quantification; Electrochemical redox probes; Living cells; Whole blood analysis; BIOLOGY; H2S; ANTIBIOTICS; CHEMISTRY; SUBSTRATE; BACTERIA; FLUORIDE; SENSOR; GUIDE;
D O I
10.1016/j.bios.2017.05.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Hydrogen sulfide (H2S) was discovered as a third gasotransmitter in biological systems and recent years have seen a growing interest to understand its physiological and pathological functions. However, one major limiting factor is the lack of robust sensors to quantitatively track its production in real-time. We described a facile electrochemical assay based on latent redox probe approach for highly specific and sensitive quantification in living cells. Two chemical probes, Azido Benzyl ferrocene carbamate (ABFC) and N-alkyl Azido Benzyl ferrocene carbamate (NABFC) composed of azide trigger group were designed. H2S molecules specifically triggered the release of reporters from probes and the current response was monitored using graphene oxide film modified electrode as transducer. The detection limits are 0.32 mu M (ABFC) and 0.076 mu M (NABFC) which are comparable to those of current sensitive methods. The probes are successful in the determination of H2S spiked in whole human blood, fetal bovine serum, and E. coli. The continuous monitoring and quantification of endogenous H2S production in E. coli were successfully accomplished. This work lays first step stone towards real-time electrochemical quantification of endogenous H2S in living cells, thus hold great promise in the analytical aspects of H2S.
引用
收藏
页码:233 / 238
页数:6
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