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本文引用的文献

1
Multi-shell model of ion-induced nucleic acid condensation.离子诱导核酸凝聚的多壳层模型
J Chem Phys. 2016 Apr 21;144(15):155101. doi: 10.1063/1.4945382.
2
Understanding nucleic acid structural changes by comparing wide-angle x-ray scattering (WAXS) experiments to molecular dynamics simulations.通过将广角X射线散射(WAXS)实验与分子动力学模拟进行比较来理解核酸结构变化。
J Chem Phys. 2016 May 28;144(20):205102. doi: 10.1063/1.4950814.
3
Inhomogeneous screening near the dielectric interface.电介质界面附近的非均匀屏蔽
J Chem Phys. 2016 Apr 7;144(13):134902. doi: 10.1063/1.4945011.
4
Direct evidence for sequence-dependent attraction between double-stranded DNA controlled by methylation.由甲基化控制的双链DNA之间序列依赖性吸引的直接证据。
Nat Commun. 2016 Mar 22;7:11045. doi: 10.1038/ncomms11045.
5
The structure and intermolecular forces of DNA condensates.DNA凝聚物的结构与分子间作用力。
Nucleic Acids Res. 2016 Mar 18;44(5):2036-46. doi: 10.1093/nar/gkw081. Epub 2016 Feb 15.
6
Improved Parameterization of Amine-Carboxylate and Amine-Phosphate Interactions for Molecular Dynamics Simulations Using the CHARMM and AMBER Force Fields.使用 CHARMM 和 AMBER 力场改进用于分子动力学模拟的胺-羧酸酯和胺-磷酸盐相互作用的参数化。
J Chem Theory Comput. 2016 Jan 12;12(1):430-43. doi: 10.1021/acs.jctc.5b00967. Epub 2015 Dec 16.
7
Mg(II) and Ni(II) induce aggregation of poly(rA)poly(rU) to either tetra-aggregate or triplex depending on the metal ion concentration.镁离子(Mg(II))和镍离子(Ni(II))会根据金属离子浓度诱导聚腺苷酸-聚尿苷酸(poly(rA)poly(rU))聚集形成四聚体或三链体。
J Inorg Biochem. 2015 Oct;151:115-22. doi: 10.1016/j.jinorgbio.2015.05.001. Epub 2015 May 9.
8
Building Water Models: A Different Approach.构建水模型:一种不同的方法。
J Phys Chem Lett. 2014 Nov 6;5(21):3863-3871. doi: 10.1021/jz501780a. Epub 2014 Oct 16.
9
Endogenous polyamine function--the RNA perspective.内源性多胺功能——RNA视角
Nucleic Acids Res. 2014 Oct;42(18):11275-90. doi: 10.1093/nar/gku837. Epub 2014 Sep 17.
10
Why double-stranded RNA resists condensation.为何双链RNA能抵抗凝聚作用。
Nucleic Acids Res. 2014;42(16):10823-31. doi: 10.1093/nar/gku756. Epub 2014 Aug 14.

精胺凝聚DNA,但不凝聚RNA双链体。

Spermine Condenses DNA, but Not RNA Duplexes.

作者信息

Katz Andrea M, Tolokh Igor S, Pabit Suzette A, Baker Nathan, Onufriev Alexey V, Pollack Lois

机构信息

School of Applied and Engineering Physics, Cornell University, Ithaca, New York.

Department of Computer Science, Virginia Tech, Blacksburg, Virginia.

出版信息

Biophys J. 2017 Jan 10;112(1):22-30. doi: 10.1016/j.bpj.2016.11.018.

DOI:10.1016/j.bpj.2016.11.018
PMID:28076812
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5232352/
Abstract

Interactions between the polyamine spermine and nucleic acids drive important cellular processes. Spermine condenses DNA and some RNAs, such as poly(rA):poly(rU). A large fraction of the spermine present in cells is bound to RNA but apparently does not condense it. Here, we study the effect of spermine binding to short duplex RNA and DNA, and compare our findings with predictions of molecular-dynamics simulations. When small numbers of spermine are introduced, RNA with a designed sequence containing a mixture of 14 GC pairs and 11 AU pairs resists condensation relative to DNA of an equivalent sequence or to 25 bp poly(rA):poly(rU) RNA. A comparison of wide-angle x-ray scattering profiles with simulation results suggests that spermine is sequestered deep within the major groove of mixed-sequence RNA. This prevents condensation by limiting opportunities to bridge to other molecules and stabilizes the RNA by locking it into a particular conformation. In contrast, for DNA, simulations suggest that spermine binds externally to the duplex, offering opportunities for intermolecular interaction. The goal of this study is to explain how RNA can remain soluble and available for interaction with other molecules in the cell despite the presence of spermine at concentrations high enough to precipitate DNA.

摘要

多胺精胺与核酸之间的相互作用驱动着重要的细胞过程。精胺可使DNA和一些RNA(如聚(rA):聚(rU))凝聚。细胞中存在的大部分精胺与RNA结合,但显然不会使其凝聚。在此,我们研究了精胺与短双链RNA和DNA结合的影响,并将我们的发现与分子动力学模拟的预测结果进行比较。当引入少量精胺时,含有14个GC对和11个AU对混合物的设计序列RNA相对于等效序列的DNA或25bp聚(rA):聚(rU)RNA更能抵抗凝聚。广角X射线散射图谱与模拟结果的比较表明,精胺被隔离在混合序列RNA的大沟深处。这通过限制与其他分子桥接的机会来防止凝聚,并通过将RNA锁定在特定构象中来使其稳定。相比之下,对于DNA,模拟表明精胺在双链体外部结合,为分子间相互作用提供了机会。本研究的目的是解释在精胺浓度高到足以使DNA沉淀的情况下,RNA如何仍能保持可溶并可与细胞中的其他分子相互作用。