Identification of Different Protein Molecules Using MoS2-Graphene Heterostructure Nanopores

Chaoming Gu, Zhoubin Yu, Zhi Ye, Xiaojie Li, C. Jin, Yang Liu, Xin Zhu, Zhen Cao, Xiao Yu
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Abstract

MoS2-graphene heterostructure nanopores have shown the potential of detecting single protein molecules with high spatial resolution and slow translocation speed. In this work, we use this new type of nanopore to identify different protein molecules including bovine serum albumin (BSA) and Immunoglobulin G (IgG). The heterostructure nanopores are drilled by FIB and TEM with diameter of ~12 nm. The statistical and single-signal analyses of the single protein molecules translocation are conducted. The results demonstrate that due to stronger interaction with the heterostructure, IgG molecules have much longer dwell time than BSA, while the complete translocation of IgG becomes harder, leading to obvious lower current blockage. Our analysis indicates that heterostructure nanopores are capable of identifying and distinguishing different types of proteins.
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利用二硫化钼-石墨烯异质结构纳米孔鉴定不同蛋白质分子
mos2 -石墨烯异质结构纳米孔具有较高的空间分辨率和较慢的易位速度,具有检测单个蛋白质分子的潜力。在这项工作中,我们使用这种新型纳米孔来识别不同的蛋白质分子,包括牛血清白蛋白(BSA)和免疫球蛋白G (IgG)。利用FIB和TEM对其进行了孔径约为12 nm的异质结构纳米孔的钻取。对单蛋白分子易位进行了统计分析和单信号分析。结果表明,由于与异质结构的相互作用更强,IgG分子的停留时间比BSA长得多,而IgG的完全易位变得更加困难,导致电流阻塞明显降低。我们的分析表明,异质结构纳米孔能够识别和区分不同类型的蛋白质。
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