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ACS Nano. 2016 Apr 26;10(4):4644-51. doi: 10.1021/acsnano.6b00940. Epub 2016 Apr 15.
2
Fluctuating bottleneck model studies on kinetics of DNA escape from α-hemolysin nanopores.关于DNA从α-溶血素纳米孔逃逸动力学的波动瓶颈模型研究。
J Chem Phys. 2015 Nov 14;143(18):184908. doi: 10.1063/1.4935118.
3
Thermal Motion of DNA in an MspA Pore.DNA在MspA孔道中的热运动。
Biophys J. 2015 Oct 6;109(7):1439-45. doi: 10.1016/j.bpj.2015.08.019.
4
Subangstrom single-molecule measurements of motor proteins using a nanopore.使用纳米孔对运动蛋白进行亚埃级单分子测量。
Nat Biotechnol. 2015 Oct;33(10):1073-5. doi: 10.1038/nbt.3357. Epub 2015 Sep 28.
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Excess white noise to probe transport mechanisms in a membrane channel.
Phys Rev E Stat Nonlin Soft Matter Phys. 2015 Jun;91(6):062704. doi: 10.1103/PhysRevE.91.062704. Epub 2015 Jun 8.
6
DNA stretching and optimization of nucleobase recognition in enzymatic nanopore sequencing.酶促纳米孔测序中DNA拉伸与核碱基识别的优化
Nanotechnology. 2015 Feb 27;26(8):084002. doi: 10.1088/0957-4484/26/8/084002. Epub 2015 Feb 3.
7
Decoding long nanopore sequencing reads of natural DNA.解码天然DNA的长纳米孔测序读数。
Nat Biotechnol. 2014 Aug;32(8):829-33. doi: 10.1038/nbt.2950. Epub 2014 Jun 25.
8
Molecular dynamics study of MspA arginine mutants predicts slow DNA translocations and ion current blockades indicative of DNA sequence.MspA 精氨酸突变体的分子动力学研究预测了 DNA 缓慢易位和离子电流阻断,表明存在 DNA 序列。
ACS Nano. 2012 Aug 28;6(8):6960-8. doi: 10.1021/nn3019943. Epub 2012 Jul 13.
9
Reading DNA at single-nucleotide resolution with a mutant MspA nanopore and phi29 DNA polymerase.利用突变型 MspA 纳米孔和 phi29 DNA 聚合酶实现单核苷酸分辨率下的 DNA 读取。
Nat Biotechnol. 2012 Mar 25;30(4):349-53. doi: 10.1038/nbt.2171.
10
Automated forward and reverse ratcheting of DNA in a nanopore at 5-Å precision.在纳米孔中以 5Å 的精度实现 DNA 的自动正向和反向棘轮作用。
Nat Biotechnol. 2012 Feb 14;30(4):344-8. doi: 10.1038/nbt.2147.

被困于MspA纳米孔中的单链DNA的电荷、扩散及电流波动

Charge, Diffusion, and Current Fluctuations of Single-Stranded DNA Trapped in an MspA Nanopore.

作者信息

Fleming Stephen J, Lu Bo, Golovchenko Jene A

机构信息

Department of Physics, Harvard University, Cambridge, Massachusetts.

Department of Physics, Harvard University, Cambridge, Massachusetts; School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts.

出版信息

Biophys J. 2017 Jan 24;112(2):368-375. doi: 10.1016/j.bpj.2016.12.007.

DOI:10.1016/j.bpj.2016.12.007
PMID:28122222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5266147/
Abstract

We report effective charges and diffusion constants of several different single-stranded DNA oligonucleotides trapped in an MspA nanopore. Nucleotide identity is found to have a substantial influence on effective charges and diffusion constants. These quantities are determined from escape time experiments for a DNA molecule attached to a NeutrAvidin molecule that, unlike the DNA, does not pass through the pore. Correlations are reported between oligonucleotide effective charges and current blockages, and between their diffusion constants and DNA-induced current blockage fluctuations. We also report an unanticipated source of current fluctuations that reflects a discrete blockage current level structure. We posit that this is associated with interactions between the NeutrAvidin molecule and the MspA nanopore.

摘要

我们报告了被困在MspA纳米孔中的几种不同单链DNA寡核苷酸的有效电荷和扩散常数。发现核苷酸身份对有效电荷和扩散常数有重大影响。这些量是通过对连接到中性抗生物素蛋白分子上的DNA分子进行逃逸时间实验确定的,与DNA不同,中性抗生物素蛋白分子不会穿过孔。报告了寡核苷酸有效电荷与电流阻断之间以及它们的扩散常数与DNA诱导的电流阻断波动之间的相关性。我们还报告了一个意外的电流波动源,它反映了离散的阻断电流水平结构。我们推测这与中性抗生物素蛋白分子和MspA纳米孔之间的相互作用有关。