Departments of Chemistry, Beijing Normal University, People's Republic of China.
J Phys Chem B. 2010 Aug 5;114(30):9926-33. doi: 10.1021/jp104360q.
Mediated electrochemical biosensors consisting of two enzymes have attracted increasing interest because of their wider applicability. In this work, concanavalin A (Con A) and two glycoenzymes, horseradish peroxidase (HRP) and glucose oxidase (GOD), were assembled into {Con A/HRP/Con A/GOD}(n) layer-by-layer films on an electrode surface mainly by lectin-sugar biospecific interaction between Con A and glycoenzymes. The cyclic voltammetry (CV) response of Fe(CN)(6)(3-) at the bienzyme film electrodes was very sensitive to the environmental pH: at pH 4.0, the CV peak currents were quite large and the films were at the "on" state; at pH 8.0, however, the electrochemical response was significantly suppressed and the films were at the "off" state. By switching the film electrodes in solution between pH 4.0 and pH 8.0, the CV peak currents cycled between the on and off states, demonstrating the reversible pH-sensitive on-off switching. The pH-responsive property of the films toward the probe could be used to switch the on-off bioelectrocatalysis of glucose. That is, the electrochemical oxidation of glucose catalyzed by GOD and HRP in the films mediated by Fe(CN)(6)(3-) in solution could be controlled by changing the surrounding pH, allowing the reversible transition of bioelectrocatalysis between the on and off states. CV, electrochemical impedance spectroscopy, amperometry, and quartz crystal microbalance studies were used to characterize the {Con A/HRP/Con A/GOD}(n) films. The mechanism of pH-sensitive switchable behavior of the films was further explored by comparative experiments and should be attributed to the different electrostatic interactions between the films and the probes at different pH values. This pH-switchable bioelectrocatalysis based on the smart bienzyme interface may pave the way for designing novel controllable biosensors.
基于两种酶的介体电化学生物传感器由于其更广泛的适用性而引起了越来越多的关注。在这项工作中,刀豆球蛋白 A(Con A)和两种糖酶,辣根过氧化物酶(HRP)和葡萄糖氧化酶(GOD),主要通过凝集素-糖生物特异性相互作用组装在电极表面上的{Con A/HRP/Con A/GOD}(n)层状膜中。双酶膜电极上的 Fe(CN)(6)(3-)的循环伏安(CV)响应对环境 pH 非常敏感:在 pH 4.0 时,CV 峰电流非常大,膜处于“开”状态;然而,在 pH 8.0 时,电化学响应受到显著抑制,膜处于“关”状态。通过在溶液中将膜电极在 pH 4.0 和 pH 8.0 之间切换,CV 峰电流在开和关状态之间循环,证明了可逆的 pH 敏感开-关切换。膜对探针的 pH 响应特性可用于切换葡萄糖的开-关生物电化学催化。也就是说,溶液中 Fe(CN)(6)(3-)介导的 GOD 和 HRP 在膜中的电化学氧化可以通过改变周围 pH 来控制,从而允许生物电化学催化在开和关状态之间可逆转换。CV、电化学阻抗谱、安培法和石英晶体微天平研究用于表征{Con A/HRP/Con A/GOD}(n)膜。通过比较实验进一步探讨了膜的 pH 敏感开关行为的机制,这归因于不同 pH 值下膜与探针之间的不同静电相互作用。这种基于智能双酶界面的 pH 可切换生物电化学催化可能为设计新型可控生物传感器铺平道路。