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利用 NMR 研究单链 RNA 螺旋结的结构动力学。

Structural dynamics of a single-stranded RNA-helix junction using NMR.

机构信息

Chemical Biology Doctoral Program, University of Michigan, Ann Arbor, Michigan 48109, USA.

Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

RNA. 2014 Jun;20(6):782-91. doi: 10.1261/rna.043711.113. Epub 2014 Apr 17.

Abstract

Many regulatory RNAs contain long single strands (ssRNA) that adjoin secondary structural elements. Here, we use NMR spectroscopy to study the dynamic properties of a 12-nucleotide (nt) ssRNA tail derived from the prequeuosine riboswitch linked to the 3' end of a 48-nt hairpin. Analysis of chemical shifts, NOE connectivity, (13)C spin relaxation, and residual dipolar coupling data suggests that the first two residues (A25 and U26) in the ssRNA tail stack onto the adjacent helix and assume an ordered conformation. The following U26-A27 step marks the beginning of an A6-tract and forms an acute pivot point for substantial motions within the tail, which increase toward the terminal end. Despite substantial internal motions, the ssRNA tail adopts, on average, an A-form helical conformation that is coaxial with the helix. Our results reveal a surprising degree of structural and dynamic complexity at the ssRNA-helix junction, which involves a fine balance between order and disorder that may facilitate efficient pseudoknot formation on ligand recognition.

摘要

许多调控 RNA 包含与二级结构元件毗邻的长单链 (ssRNA)。在这里,我们使用 NMR 光谱学来研究来自 prequeuosine 核糖开关的 12 个核苷酸 (nt) ssRNA 尾巴的动态特性,该核糖开关连接到 48 个核苷酸发夹的 3' 端。化学位移、NOE 连接性、(13)C 自旋弛豫和残差偶极耦合数据的分析表明,ssRNA 尾巴的前两个残基 (A25 和 U26) 堆积在相邻的螺旋上,并呈现出有序的构象。接下来的 U26-A27 步标志着 A6- 链的开始,并形成了尾巴内大量运动的锐角枢轴点,这些运动在末端方向增加。尽管存在大量的内部运动,但 ssRNA 尾巴平均采用与螺旋共轴的 A 型螺旋构象。我们的结果揭示了 ssRNA- 螺旋连接点处惊人的结构和动态复杂性,这涉及到有序和无序之间的精细平衡,可能有助于在配体识别时有效地形成假结。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/4024633/d3223a57babd/782f01.jpg

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