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聚合物在电场作用下通过拥挤通道的迁移。

Translocation of a Polymer through a Crowded Channel under Electrical Force.

机构信息

Department of Physics, School of Information and Electronic Engineering, Zhejiang Gongshang University, Hangzhou 310018, China.

Department of Applied Chemistry, School of Food Science and Biotechnology, Zhejiang Gongshang University, Hangzhou 310018, China.

出版信息

Biomed Res Int. 2017;2017:5267185. doi: 10.1155/2017/5267185. Epub 2017 Mar 26.

DOI:10.1155/2017/5267185
PMID:28459062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5385253/
Abstract

The translocation of a polymer chain through a crowded cylindrical channel is studied using the Langevin dynamics simulations. The influences of the field strength , the chain length , and the crowding extent ρ on the translocation time are evaluated, respectively. Scaling relation τ ~ is observed. With the crowding extent ρ increasing, the scaling exponent α becomes large. It is found that, for noncrowded channel, translocation probability drops when the field strength becomes large. However, for high-crowded channel, it is the opposite. Moreover, the translocation time and the average translocation time for all segments both have exponential growth with the crowding extent. The investigation of shape factor 〈δ〉 shows maximum value with increasing of the number of segments outside . At last, the number of segments inside channel in the process of translocation is calculated and a peak is observed. All the information from the study may benefit protein translocation.

摘要

使用 Lange因动力学模拟研究了聚合物链通过拥挤的圆柱形通道的迁移。分别评估了场强 、链长和拥挤程度 ρ 对迁移时间的影响。观察到标度关系 τ ~ 。随着拥挤程度 ρ 的增加,标度指数 α 变大。发现,对于非拥挤的通道,当场强增大时,迁移概率下降。然而,对于高拥挤的通道,情况则相反。此外,迁移时间和所有片段的平均迁移时间都随拥挤程度呈指数增长。形状因子 〈δ〉 的研究表明,随着外部片段数的增加,其最大值也随之增加。最后,计算了在迁移过程中通道内的片段数 ,并观察到一个峰值。从这项研究中获得的所有信息都可能有利于蛋白质的转位。

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本文引用的文献

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Detecting protein-protein interactions with a novel matrix-based protein sequence representation and support vector machines.利用一种基于新型矩阵的蛋白质序列表示法和支持向量机检测蛋白质-蛋白质相互作用。
Biomed Res Int. 2015;2015:867516. doi: 10.1155/2015/867516. Epub 2015 Apr 27.
2
Integrating genomics and proteomics data to predict drug effects using binary linear programming.使用二元线性规划整合基因组学和蛋白质组学数据以预测药物效果。
PLoS One. 2014 Jul 18;9(7):e102798. doi: 10.1371/journal.pone.0102798. eCollection 2014.
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Translocation of α-helix chains through a nanopore.
α-螺旋链通过纳米孔的转位。
J Chem Phys. 2010 Oct 21;133(15):154903. doi: 10.1063/1.3493332.
4
Translocation dynamics with attractive nanopore-polymer interactions.具有吸引性纳米孔 - 聚合物相互作用的转位动力学。
Phys Rev E Stat Nonlin Soft Matter Phys. 2008 Dec;78(6 Pt 1):061918. doi: 10.1103/PhysRevE.78.061918. Epub 2008 Dec 19.
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Dynamics of DNA translocation through an attractive nanopore.
Phys Rev E Stat Nonlin Soft Matter Phys. 2008 Dec;78(6 Pt 1):061911. doi: 10.1103/PhysRevE.78.061911. Epub 2008 Dec 9.
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A Monte Carlo algorithm to study polymer translocation through nanopores. II. Scaling laws.一种用于研究聚合物通过纳米孔转位的蒙特卡罗算法。II. 标度律。
J Chem Phys. 2008 May 28;128(20):205103. doi: 10.1063/1.2927878.
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Sequence effects on the forced translocation of heteropolymers through a small channel.序列对杂聚物通过小通道的强制转运的影响。
J Chem Phys. 2008 May 7;128(17):175103. doi: 10.1063/1.2912069.
8
Polymer translocation through a cylindrical channel.聚合物通过圆柱形通道的转运。
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9
Sequence dependence of DNA translocation through a nanopore.DNA通过纳米孔转运的序列依赖性。
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10
The effect of hydrodynamic interactions on the dynamics of DNA translocation through pores.流体动力学相互作用对DNA通过孔道转运动力学的影响。
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