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Conductive atomic force microscopy study of plastocyanin molecules adsorbed on gold electrode

机译:导电原子力显微镜研究金电极上吸附的质体蓝素分子

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摘要

The electrical conduction of mutant plastocyanin molecules self-assembled on gold was measured by conductive atomic force microscopy. The copper protein molecules, able to bind to gold through an engineered S-S group, were immobilised on Au(111) substrates to form a dense monolayer, which was contacted by a conductive atomic force microscopy tip at controlled force. Specifically, the electronic conduction of the gold coated tip-plastocyanin-Au(111) junction was well characterised between +1 and -1 V for increasing compressional forces. The conduction varies slightly within the force range of 3-9 nN, while it rapidly increases above these force values. The occurrence of a jump in mutant plastocyanin conduction at a critical force value, suggests that the current transport mechanism through the bioelectronic junction can be dominated by protein mechanical characteristics and/or by considerable variations in the protein conduction upon molecular deformation. By operating in imaging mode, we have obtained good topographic images of the protein self-assembled on Au(111) surface and for the first time simultaneous current images were recorded. Remarkably, a correspondence between the biomolecuies observed in the topography images and the current spots was found for negative bias.
机译:通过导电原子力显微镜测量在金上自组装的突变体质体蓝素分子的电导率。能够通过工程S-S基团与金结合的铜蛋白分子被固定在Au(111)基底上以形成致密的单层,导电原子力显微镜尖端以受控的力使其接触。具体来说,镀金的尖端-质体蓝蛋白-Au(111)结的电子传导在+1和-1 V之间被很好地表征,以增加压缩力。在3-9 nN的力范围内,传导略有变化,而在这些力值以上时,传导迅速增加。在临界力值下突变体质体蓝素传导的跳跃的发生表明,通过生物电子连接的电流转运机制可以由蛋白质的机械特性和/或分子变形后蛋白质传导的显着变化所控制。通过在成像模式下操作,我们获得了自组装在Au(111)表面上的蛋白质的良好形貌图像,并且首次记录了同时电流图像。显着地,发现在形貌图像中观察到的生物分子与当前斑点之间的对应关系为负偏压。

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