Suppr超能文献

溶液中错配DNA八聚体d(m5C-G-m5C-G-A-G-m5C-G)多晶型行为的核磁共振研究。B-双链体和发夹形式。

An NMR study of polymorphous behaviour of the mismatched DNA octamer d(m5C-G-m5C-G-A-G-m5C-G) in solution. The B-duplex and hairpin forms.

作者信息

Orbons L P, van der Marel G A, van Boom J H, Altona C

机构信息

Gorlaeus Laboratories, Leiden University, The Netherlands.

出版信息

Eur J Biochem. 1987 Dec 30;170(1-2):225-39. doi: 10.1111/j.1432-1033.1987.tb13690.x.

Abstract

By means of one- and two-dimensional NMR spectroscopy the solution structures of the partly self-complementary octamer d(m5C-G-m5C-G-A-G-m5C-G) were investigated. It is shown that this DNA fragment, under conditions of high DNA concentration (8 mM DNA) and/or high ionic strength prefers to adopt a duplex structure. At low DNA concentration (0.4 mM DNA), the duplex exists in a 1:1 slow equilibrium with a monomeric hairpin form. Addition of salt destabilizes the hairpin structure in favour of the dimer. At high temperatures the hairpin form, as well as the dimer structure, exist in a fast equilibrium with the random-coil form. For the hairpin/random-coil equilibrium a Tm of 329 K and a delta H degree of -121 kJ.mol-1 were deduced. These thermodynamic parameters are independent of the DNA concentration, as is expected for a monomeric structure. For the dimer to coil transition a Tm of 359 K (1 M DNA) and a delta H degree of -285 kJ.mol duplex-1 were derived. The thermodynamic data of the hairpin-coil transition mutually agree with those recently reported for the hairpin to random coil equilibrium of the DNA octamer d(m5C-G-m5C-G-T-G-m5C-G) [Orbons, L. P. M., van der Marel, G. A., van Boom, J. H. & Altona, C. (1987) J. Biomol. Struct. Dyns. 4, 939-963]. It is demonstrated that the dimer structure exhibits B-DNA characteristics, as is witnessed by the NOESY experiments and the analysis of the proton-proton coupling data. It is shown that the base-pair formation of the G x A mismatches is anti-anti. A comparison of 1H and 31P chemical-shift data of the title compound with those of a well-characterized B-DNA structure reveals large differences in the dm5C(3)-dG(4)-dA(5) part of the mismatched dimer structure. These differences apparently indicate some major local structural changes due to the incorporation of the G x A mismatches. Under the most extreme conditions used (i.e. up to 3 M NaCl or 75% CH3OH in the presence of 10 mM MgCl2) no Z-DNA structure was observed. It is shown that the structural features of the hairpin form of the title compound mimic those of the hairpin structure of d(m5C-G-m5C-G-T-G-m5C-G). An energy-minimized model of the hairpin form is given.

摘要

通过一维及二维核磁共振光谱法研究了部分自我互补的八聚体d(m5C-G-m5C-G-A-G-m5C-G)的溶液结构。结果表明,在高DNA浓度(8 mM DNA)和/或高离子强度条件下,该DNA片段倾向于形成双链结构。在低DNA浓度(0.4 mM DNA)时,双链与单体发夹形式以1:1的慢平衡存在。加入盐会使发夹结构不稳定,有利于二聚体的形成。在高温下,发夹形式以及二聚体结构与无规卷曲形式快速平衡。对于发夹/无规卷曲平衡,推导出的熔点为329 K,焓变为 -121 kJ·mol-1。这些热力学参数与DNA浓度无关,这对于单体结构来说是预期的。对于二聚体到卷曲的转变,得出熔点为359 K(1 M DNA),双链的焓变为 -285 kJ·mol-1。发夹 - 卷曲转变的热力学数据与最近报道的DNA八聚体d(m5C-G-m5C-G-T-G-m5C-G)从发夹到无规卷曲平衡的数据相互一致[Orbons, L. P. M., van der Marel, G. A., van Boom, J. H. & Altona, C. (1987) J. Biomol. Struct. Dyns. 4, 939 - 963]。通过NOESY实验和质子 - 质子耦合数据分析表明,二聚体结构具有B - DNA特征。结果表明,G×A错配的碱基对形成是反式 - 反式。将标题化合物的1H和31P化学位移数据与特征明确的B - DNA结构的数据进行比较,发现错配二聚体结构的dm5C(3)-dG(4)-dA(5)部分存在很大差异。这些差异显然表明由于G×A错配的掺入导致了一些主要的局部结构变化。在使用的最极端条件下(即在10 mM MgCl2存在下高达3 M NaCl或75% CH3OH)未观察到Z - DNA结构。结果表明,标题化合物发夹形式的结构特征与d(m5C-G-m5C-G-T-G-m5C-G)的发夹结构相似。给出了发夹形式的能量最小化模型。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验