Department of Biological Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700032, India.
Langmuir. 2011 Aug 16;27(16):9681-6. doi: 10.1021/la202045a. Epub 2011 Jul 19.
Utility of ferritin in molecular electronics, especially in single molecule electronics based devices, has recently been proposed, since the iron core of holoferritin is semiconducting in nature. However, the practical aspects, e.g., how its electronic properties can be varied/tuned, need to be better addressed. In this direction, we have performed direct tunneling experiments using scanning tunneling microscopy (STM) and scanning tunneling spectroscopy (STS) on several metal core reconstituted ferritins, where the reconstitution has been carried out using biocompatible metals like copper, cobalt, and manganese that are found naturally in the human body. We show, for the first time, that, by metal core reconstitution of the ferritin protein, the band gap of the protein can be tuned to different values (here, within the range 1.17-0.00 eV, considering iron-containing holoferritin and apoferritin as well). From the respective current-voltage curves and the well-defined band gaps, clear distinction can be made among the five different ferritins indicating that the metal core has direct contribution in the observed electrical conductivities of ferritins. It is further revealed that the electrical conductivities of the reconstituted ferritins are of the same order as that for the free metal conductivities, meaning that the relative changes in the free metal conductivities are reflected in the contributions of the metals in protein shell-confinement (i.e., the ∼8 nm core of ferritin). This finding could lead to a strategy for fine-tuning ferritin band gap by preselecting a metal on the basis of the free metal conductivity values.
铁蛋白在分子电子学,特别是基于单分子电子学的器件中的应用最近已经被提出,因为天然的脱铁铁蛋白的铁核具有半导体性质。然而,还需要更好地解决其实用性问题,例如如何改变/调整其电子特性。在这个方向上,我们已经使用扫描隧道显微镜(STM)和扫描隧道光谱(STS)对几种金属核心重构的铁蛋白进行了直接隧道实验,其中重构是使用生物相容性金属(如铜、钴和锰)进行的,这些金属在人体内天然存在。我们首次表明,通过铁蛋白蛋白的金属核心重构,可以将蛋白的带隙调谐到不同的值(这里,在考虑含铁的全铁蛋白和脱铁蛋白的情况下,在 1.17-0.00 eV 的范围内)。从各自的电流-电压曲线和明确定义的带隙,可以清楚地区分五种不同的铁蛋白,表明金属核心直接参与了铁蛋白观察到的电导率。进一步揭示,重构的铁蛋白的电导率与自由金属的电导率处于同一数量级,这意味着自由金属电导率的相对变化反映在金属在蛋白质壳限制中的贡献(即,铁蛋白的∼8nm 核心)。这一发现可能会导致一种通过基于自由金属电导率值预选金属来微调铁蛋白带隙的策略。