纳米孔
聚合物
高分子物理
布朗动力学
布朗运动
纳米尺度
化学物理
DNA
朗之万动力
分子
纳米技术
动力学(音乐)
物理
材料科学
化学
统计物理学
量子力学
生物化学
核磁共振
声学
作者
Kaikai Chen,Ining A. Jou,Niklas Ermann,M. Muthukumar,Ulrich F. Keyser,Nicholas A. W. Bell
出处
期刊:Nature Physics
[Springer Nature]
日期:2021-06-24
卷期号:17 (9): 1043-1049
被引量:49
标识
DOI:10.1038/s41567-021-01268-2
摘要
The transport of polymers across nanoscale pores underpins many biological processes, such as the ejection of bacteriophage DNA into a host cell and the transfer of genes between bacteria. The movement of polymers into and out of confinement is also the basis for a wide range of sensing technologies used for single-molecule detection and sequencing. Acquiring an accurate understanding of the translocation dynamics is an essential step in the quantitative analysis of polymer structure, including the localization of binding sites or sequences. Here we use synthetic nanopores and nanostructured DNA molecules to directly measure the velocity profile of driven polymer translocation through synthetic nanopores. Our results reveal a two-stage behaviour in which the translocation initially slows with time before accelerating close to the end of the process. We also find distinct local velocity correlations as the DNA polymer chain passes through the nanopore. Brownian dynamics simulations show that the two-stage behaviour is associated with tension propagation, with correlations arising from the random-walk conformation in which the DNA begins. A study of the dynamics of polymer translocation through synthetic nanopores provides a direct observation of tension propagation—a non-equilibrium description of the process of unfolding that a polymer undergoes during translocation.
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