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Conductive supports for combined AFM-SECM on biological membranes

机译:用于生物膜上的组合AFM-SECM的导电载体

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Four different conductive supports are analysed regarding their suitability for combined atomic force and scanning electrochemical microscopy ( AFM-SECM) on biological membranes. Highly oriented pyrolytic graphite ( HOPG), MoS2, template stripped gold, and template stripped platinum are compared as supports for high resolution imaging of reconstituted membrane proteins or native membranes, and as electrodes for transferring electrons from or to a redox molecule. We demonstrate that high resolution topographs of the bacterial outer membrane protein F can be recorded by contact mode AFM on all four supports. Electrochemical feedback experiments with conductive cantilevers that feature nanometre-scale electrodes showed fast re-oxidation of the redox couple Ru(NH3)(6)(3+)/2(+) with the two metal supports after prolonged immersion in electrolyte. In contrast, the re-oxidation rates decayed quickly to unpractical levels with HOPG or MoS2 under physiological conditions. On HOPG we observed heterogeneity in the re-oxidation rate of the redox molecules with higher feedback currents at stEP 3edges. The latter results demonstrate the capability of conductive cantilevers with small electrodes to measure minor variations in an SECM signal and to relate them to nanometre-scale features in a simultaneously recorded AFM topography. Rapid decay of re-oxidation rate and surface heterogeneity make HOPG or MoS2 less attractive for combined AFM-SECM experiments on biological membranes than template stripped gold or platinum supports.
机译:分析了四种不同的导电载体在生物膜上的组合原子力和扫描电化学显微镜(AFM-SECM)的适用性。比较了高取向的热解石墨(HOPG),MoS2,脱模金和脱模铂,它们是重构膜蛋白或天然膜高分辨率成像的载体,以及用于将电子从氧化还原分子转移到氧化还原分子的电极。我们证明了细菌外膜蛋白F的高分辨率地形图可以通过在所有四个支持上的接触模式AFM进行记录。带有纳米级电极的导电悬臂的电化学反馈实验表明,长时间浸泡在电解质中后,氧化还原对Ru(NH3)(6)(3 +)/ 2(+)与两个金属支持物快速重新氧化。相反,在生理条件下,HOPG或MoS2的再氧化速率迅速下降至不切实际的水平。在HOPG上,我们在stEP 3edge处观察到了具有较高反馈电流的氧化还原分子的再氧化速率的异质性。后一结果证明了带有小电极的导电悬臂能够测量SECM信号中的微小变化,并将它们与同时记录的AFM形貌中的纳米级特征相关联。与模板剥离的金或铂载体相比,重新氧化速率和表面异质性的快速衰减使得HOPG或MoS2对于在生物膜上进行的AFM-SECM组合实验的吸引力较小。

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