Department of Life Sciences, Institute of Genome Sciences and Institute of Biomedical Informatics, National Yang-Ming University, Taipei 112, Taiwan.
Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan.
Sci Rep. 2017 Jan 4;7:39792. doi: 10.1038/srep39792.
Proteins are of interest in nano-bio electronic devices due to their versatile structures, exquisite functionality and specificity. However, quantum transport measurements produce conflicting results due to technical limitations whereby it is difficult to precisely determine molecular orientation, the nature of the moieties, the presence of the surroundings and the temperature; in such circumstances a better understanding of the protein electron transfer (ET) pathway and the mechanism remains a considerable challenge. Here, we report an approach to mechanically drive polypeptide flip-flop motion to achieve a logic gate with ON and OFF states during protein ET. We have calculated the transmission spectra of the peptide-based molecular junctions and observed the hallmarks of electrical current and conductance. The results indicate that peptide ET follows an NC asymmetric process and depends on the amino acid chirality and α-helical handedness. Electron transmission decreases as the number of water molecules increases, and the ET efficiency and its pathway depend on the type of water-bridged H-bonds. Our results provide a rational mechanism for peptide ET and new perspectives on polypeptides as potential candidates in logic nano devices.
蛋白质因其结构多样、功能精细和特异性而成为纳米生物电子器件的研究热点。然而,由于技术限制,量子输运测量产生了相互矛盾的结果,难以精确确定分子取向、基团的性质、周围环境和温度;在这种情况下,更好地理解蛋白质电子转移(ET)途径和机制仍然是一个相当大的挑战。在这里,我们报告了一种机械驱动多肽翻转运动的方法,以在蛋白质 ET 过程中实现具有 ON 和 OFF 状态的逻辑门。我们计算了基于肽的分子结的传输谱,并观察到电流和电导的特征。结果表明,肽 ET 遵循 NC 不对称过程,并且取决于氨基酸手性和 α-螺旋手性。随着水分子数量的增加,电子传输减少,而 ET 效率及其途径取决于水桥合氢键的类型。我们的结果为肽 ET 提供了合理的机制,并为多肽作为逻辑纳米器件潜在候选物提供了新的视角。