Wang Fang, Chen Xiaoxia, Xu Yanxia, Hu Shengshui, Gao Zhinong
Department of Chemistry, Wuhan University, Wuhan 430072, PR China.
Biosens Bioelectron. 2007 Sep 30;23(2):176-82. doi: 10.1016/j.bios.2007.03.027. Epub 2007 Apr 4.
The direct electrical communication between hemoglobin (Hb) and GCE surface was achieved based on the immobilization of Hb in a cationic gemini surfactant film and characterized by electrochemical techniques. The cyclic voltammograms showed that direct electron transfer between Hb and electrode surface was obviously promoted and then a novel unmediated nitric oxide (NO) biosensor was constructed in view of this protein-based electrode. This modified electrode showed an enzyme-like activity towards the reduction of NO and its amperometric response to NO was well-behaved with a rapid response time and displaying Michaelis-Menten kinetics with a calculated Km(app) value of 84.37 micromol L(-1). The detection limit was estimated to be 2.00 x 10(-8)mol L(-1). This biosensor was behaving as expected that it had a good stability and reproducibility, a higher sensitivity and selectivity and should has a potential application in monitoring NO released from biologic samples.
通过将血红蛋白(Hb)固定在阳离子双子表面活性剂膜中,实现了血红蛋白与玻碳电极(GCE)表面之间的直接电通讯,并采用电化学技术对其进行了表征。循环伏安图表明,Hb与电极表面之间的直接电子转移得到了明显促进,基于此蛋白质基电极构建了一种新型无媒介一氧化氮(NO)生物传感器。该修饰电极对NO的还原表现出类酶活性,其对NO的安培响应良好,响应时间快,呈现米氏动力学,计算得到的Km(app)值为84.37 μmol L⁻¹。检测限估计为2.00×10⁻⁸ mol L⁻¹。该生物传感器表现出预期的良好稳定性和重现性、较高的灵敏度和选择性,在监测生物样品中释放的NO方面具有潜在应用价值。