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阳离子双子表面活性剂膜包覆血红蛋白在电极上的电子转移增强及一氧化氮生物传感器的制备

Enhanced electron transfer for hemoglobin entrapped in a cationic gemini surfactant films on electrode and the fabrication of nitric oxide biosensor.

作者信息

Wang Fang, Chen Xiaoxia, Xu Yanxia, Hu Shengshui, Gao Zhinong

机构信息

Department of Chemistry, Wuhan University, Wuhan 430072, PR China.

出版信息

Biosens Bioelectron. 2007 Sep 30;23(2):176-82. doi: 10.1016/j.bios.2007.03.027. Epub 2007 Apr 4.

Abstract

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.

摘要

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。

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