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金属离子和共溶质对G-四链体拓扑结构的影响。

Effects of metal ions and cosolutes on G-quadruplex topology.

作者信息

Fujii Taiga, Podbevšek Peter, Plavec Janez, Sugimoto Naoki

机构信息

Frontier Institute for Biomolecular Engineering Research (FIBER), Konan University, 7-1-20 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan.

Slovenian NMR Center, National Institute of Chemistry, Hajdrihova 19, SI-1000 Ljubljana, Slovenia; EN-FIST Centre of Excellence, Trg Osvobodilne fronte 13, SI-1000 Ljubljana, Slovenia.

出版信息

J Inorg Biochem. 2017 Jan;166:190-198. doi: 10.1016/j.jinorgbio.2016.09.001. Epub 2016 Sep 14.

Abstract

Topologies of G-quadruplexes depend on oligonucleotide sequences and on environmental factors, and the diversity of G-quadruplex topologies complicates investigation of functions of these nucleic acid structures. To investigate how metal ions and cosolutes regulate topologies of G-quadruplexes, we stabilized the antiparallel conformation by insertion of 2'-deoxyxanthosine and 8-oxo-2'-deoxyguanosine into selected positions of an oligonucleotide. Thermodynamic analyses of the oligonucleotide revealed that Na stabilized the antiparallel G-quadruplex, whereas K destabilized this topology. This result suggests that metal ions selectively stabilize G-quadruplex topologies with cavities between G-quartet planes of certain sizes. In the presence of KCl in 20wt% poly(ethylene glycol) with average molecular weight of 200, the antiparallel basket-type G-quadruplex conformation was not stabilized compared with the dilute condition. In the presence of NaCl, the cosolute did stabilize the G-quadruplex with respect to the dilute condition. The presented data show that metal ions and cosolutes regulate topologies of G-quadruplexes through mechanisms that depend on sizes of metal ion cavities and hydration states.

摘要

G-四链体的拓扑结构取决于寡核苷酸序列和环境因素,并且G-四链体拓扑结构的多样性使得对这些核酸结构功能的研究变得复杂。为了研究金属离子和共溶质如何调节G-四链体的拓扑结构,我们通过将2'-脱氧黄苷和8-氧代-2'-脱氧鸟苷插入寡核苷酸的选定位置来稳定反平行构象。对该寡核苷酸的热力学分析表明,Na稳定了反平行G-四链体,而K则使这种拓扑结构不稳定。这一结果表明,金属离子选择性地稳定了在特定尺寸的G-四重平面之间具有空腔的G-四链体拓扑结构。在平均分子量为200的20wt%聚乙二醇中存在KCl的情况下,与稀释条件相比,反平行篮式G-四链体构象没有得到稳定。在存在NaCl的情况下,相对于稀释条件,共溶质确实稳定了G-四链体。所呈现的数据表明,金属离子和共溶质通过取决于金属离子空腔大小和水合状态的机制来调节G-四链体的拓扑结构。

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