Sciences Chimiques de Rennes, Equipe Matière Condensée et Systèmes Electroactifs, UMR 6226 CNRS and Université de Rennes 1, Campus de Beaulieu, 35042, Rennes, France.
Chemphyschem. 2011 Feb 7;12(2):411-8. doi: 10.1002/cphc.201000779. Epub 2011 Jan 26.
Direct and remarkably fast electron transfers between a bare glassy carbon electrode and heme proteins (hemoglobin or myoglobin) are obtained by using an aqueous 1-butyl-3-methyl imidazolium tetrafluoroborate (BMI.BF(4)) ionic-liquid mixture as electrolyte. The ionic liquid is observed to play a key role in the achievement of the electron transfer. The experimental data show that the proteins are not strongly adsorbed onto the electrode surface while giving rise to sharp and well-defined redox responses. Such a finding contrasts with most of the reported works found in literature and-beyond the fundamental aspect--it may be of interest in applications where adsorption is critical. Moreover, the electrocatalytic activity of the proteins toward the reduction of oxygen and nitrite in the aqueous BMI.BF(4) mixture is evidenced, showing the potential of this simple approach for bioelectroanalytical devices.
在含有 1-丁基-3-甲基咪唑四氟硼酸盐(BMI.BF(4))的水相离子液体电解质中,裸玻碳电极与血红素蛋白(血红蛋白或肌红蛋白)之间可实现直接、快速的电子转移。实验结果表明,离子液体在实现电子转移中起着关键作用。该离子液体不会使蛋白质强烈吸附在电极表面,但却能产生尖锐而清晰的氧化还原响应。这一发现与文献中报道的大多数工作形成对比——除了基本方面之外,它在吸附至关重要的应用中可能具有意义。此外,还证明了蛋白质在 BMI.BF(4)水相混合物中对氧气和亚硝酸盐还原的电催化活性,显示了这种简单方法在生物电化学分析装置中的潜力。