Time-resolved surface-enhanced resonance Raman spectro-electrochemistry of heme proteins

Marc Grosserueschkamp, C. Nowak, W. Knoll, R. Naumann
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引用次数: 4

Abstract

Heme proteins such as cytochrome c (cc) play a fundamental role in many biological processes. Surface-enhanced resonance Raman spectroscopy (SERRS) combined with electrochemical methods is an ideal tool to study the redox processes of heme proteins. In this context we designed a new measuring cell allowing for simultaneous electrochemical manipulation and high sensitive SERRS measurements of heme proteins. The measuring cell is based on an inverted rotating disc electrode for excitation by using a confocal Raman microscope. Furthermore, we developed a SER(R)S-active silver modified silver substrate for spectro-electrochemical applications. For this purpose silver nanoparticles (AgNPs) were adsorbed on top of a planar silver surface. The substrate was optimized for an excitation wavelength of 413 nm corresponding to the resonance frequency of heme structures. An enhancement factor of 10 5 was achieved. The high performance of the new measuring cell in combination with
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血红素蛋白的时间分辨表面增强共振拉曼光谱电化学
血红素蛋白如细胞色素c (cc)在许多生物过程中起着重要作用。表面增强共振拉曼光谱(SERRS)与电化学方法相结合是研究血红素蛋白氧化还原过程的理想工具。在这种情况下,我们设计了一种新的测量细胞,允许同时进行电化学操作和高灵敏度的SERRS测量血红素蛋白。测量单元是基于一个倒置旋转圆盘电极激发使用共聚焦拉曼显微镜。此外,我们开发了一种SER(R) s活性的银修饰银衬底,用于光谱电化学应用。为此目的,银纳米颗粒(AgNPs)被吸附在平面银表面的顶部。衬底的激发波长为413 nm,与血红素结构的共振频率相对应。增强系数达到了10.5。新型测量单元的高性能与
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