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Direct evidence for heme-assisted solid-state electronic conduction in multi-heme c-type cytochromes

机译:多血红素c型细胞色素中血红素辅助固态电子传导的直接证据

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摘要

Multi-heme cytochrome c (Cytc) proteins are key for transferring electrons out of cells, to enable intracellular oxidation to proceed in the absence of O2. In these proteins most of the hemes are arranged in a linear array suggesting a facile path for electronic conduction. To test this, we studied solvent-free electron transport across two multi-heme Cytc-type proteins: MtrF (deca-heme Cytc) and STC (tetra-heme Cytc). Transport is measured across monolayers of these proteins in a solid state configuration between Au electrodes. Both proteins showed 1000× higher conductance than single heme, or heme-free proteins, but similar conductance to monolayers of conjugated organics. Conductance is found to be temperature-independent (320–80 K), suggesting tunneling as the transport mechanism. This mechanism is consistent with I–V curves modelling, results of which could be interpreted by having protein-electrode coupling as rate limiting, rather than transport within the proteins.
机译:多血红素细胞色素c(Cytc)蛋白是将电子转移出细胞的关键,以使细胞内氧化在没有O2的情况下进行。在这些蛋白质中,大多数血红素排列成线性阵列,暗示了电子传导的便捷路径。为了测试这一点,我们研究了无溶剂电子在两种多血红素Cytc型蛋白质上的迁移:MtrF(十血红素Cytc)和STC(四血红素Cytc)。在Au电极之间以固态构型测量跨这些蛋白质单层的转运。两种蛋白质均显示出比单个血红素或无血红素蛋白质高1000倍的电导率,但与共轭有机物的单层电导率相似。发现电导率与温度无关(320–80 K),表明隧穿是其传输机制。这种机制与IV曲线建模是一致的,其结果可以通过将蛋白质-电极耦合作为速率限制而不是在蛋白质内部运输来解释。

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