Tang Longhua, Yi Long, Jiang Tao, Ren Ren, Paulose Nadappuram Binoy, Zhang Bintian, Wu Jian, Liu Xu, Lindsay Stuart, Edel Joshua B, Ivanov Aleksandar P
State Key Laboratory of Modern Optical Instrumentation, College of Optical Science and Engineering, International Research Center for Advanced Photonics, Zhejiang University, Hangzhou 310027, China.
Innovation Institute for Artificial Intelligence in Medicine, Zhejiang-California International NanoSystems Institute, Zhejiang University, Hangzhou 310000, China.
Sci Adv. 2022 May 20;8(20):eabm8149. doi: 10.1126/sciadv.abm8149. Epub 2022 May 18.
Interpreting the electrical signatures of single proteins in electronic junctions has facilitated a better understanding of the intrinsic properties of proteins that are fundamental to chemical and biological processes. Often, this information is not accessible using ensemble and even single-molecule approaches. In addition, the fabrication of nanoscale single-protein junctions remains challenging as they often require sophisticated methods. We report on the fabrication of tunneling probes, direct measurement, and active control (switching) of single-protein conductance with an external field in solution. The probes allowed us to bridge a single streptavidin molecule to two independently addressable, biotin-terminated electrodes and measure single-protein tunneling response over long periods. We show that charge transport through the protein has multiple conductive pathways that depend on the magnitude of the applied bias. These findings open the door for the reliable fabrication of protein-based junctions and can enable their use in future protein-embedded bioelectronics applications.
解读电子结中单个蛋白质的电信号,有助于更好地理解蛋白质的内在特性,这些特性是化学和生物过程的基础。通常,使用整体甚至单分子方法都无法获得这些信息。此外,纳米级单蛋白质结的制造仍然具有挑战性,因为它们通常需要复杂的方法。我们报告了隧道探针的制造、单蛋白质电导的直接测量以及在溶液中利用外部场对其进行主动控制(切换)。这些探针使我们能够将单个链霉亲和素分子连接到两个可独立寻址的、生物素末端的电极上,并长时间测量单蛋白质的隧道响应。我们表明,通过蛋白质的电荷传输有多种传导途径,这取决于所施加偏压的大小。这些发现为基于蛋白质的结的可靠制造打开了大门,并使其能够用于未来嵌入蛋白质的生物电子应用。