Olson Wilma K, Esguerra Mauricio, Xin Yurong, Lu Xiang-Jun
Department of Chemistry & Chemical Biology, BioMaPS Institute for Quantitative Biology, Rutgers, The State University of New Jersey, Wright-Rieman Laboratories, 610 Taylor Road, Piscataway, NJ 08854, USA.
Methods. 2009 Mar;47(3):177-86. doi: 10.1016/j.ymeth.2008.12.003. Epub 2009 Jan 14.
Non-canonical base pairs play important roles in organizing the complex three-dimensional folding of RNA. Here, we outline methodology developed both to analyze the spatial patterns of interacting base pairs in known RNA structures and to reconstruct models from the collective experimental information. We focus attention on the structural context and deformability of the seven pairing patterns found in greatest abundance in the helical segments in a set of well-resolved crystal structures, including (i-ii) the canonical A.U and G.C Watson-Crick base pairs, (iii) the G.U wobble pair, (iv) the sheared G.A pair, (v) the A.U Hoogsteen pair, (vi) the U.U wobble pair, and (vii) the G.A Watson-Crick-like pair. The non-canonical pairs stand out from the canonical associations in terms of apparent deformability, spanning a broader range of conformational states as measured by the six rigid-body parameters used to describe the spatial arrangements of the interacting bases, the root-mean-square deviations of the base-pair atoms, and the fluctuations in hydrogen-bonding geometry. The deformabilties, the modes of base-pair deformation, and the preferred sites of occurrence depend on sequence. We also characterize the positioning and overlap of the base pairs with respect to the base pairs that stack immediately above and below them in double-helical fragments. We incorporate the observed positions of the bases, base pairs, and intervening phosphorus atoms in models to predict the effects of the non-canonical interactions on overall helical structure.
非标准碱基对在RNA复杂的三维折叠结构组织中发挥着重要作用。在此,我们概述了已开发的方法,用于分析已知RNA结构中相互作用碱基对的空间模式,并根据收集到的实验信息重建模型。我们重点关注在一组解析良好的晶体结构的螺旋片段中最丰富的七种配对模式的结构背景和可变形性,包括(i - ii)标准的A·U和G·C沃森 - 克里克碱基对、(iii)G·U摆动对、(iv)剪切的G·A对、(v)A·U霍格施泰因对、(vi)U·U摆动对以及(vii)类G·A沃森 - 克里克对。从表观可变形性方面来看,非标准碱基对比标准碱基对更为突出,通过用于描述相互作用碱基空间排列的六个刚体参数、碱基对原子的均方根偏差以及氢键几何结构的波动来衡量,非标准碱基对跨越更广泛的构象状态范围。可变形性、碱基对变形模式以及优先出现位点均取决于序列。我们还描述了在双螺旋片段中,碱基对相对于紧邻其上方和下方堆叠的碱基对的定位和重叠情况。我们将碱基、碱基对以及中间磷原子在模型中的观测位置纳入其中,以预测非标准相互作用对整体螺旋结构的影响。