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Size, shape, and flexibility of RNA structures

机译:RNA结构的大小,形状和灵活性

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Determination of sizes and flexibilities of RNA molecules is important in understanding the nature of packing in folded structures and in elucidating interactions between RNA and DNA or proteins. Using the coordinates of the structures of RNA in the Protein Data Bank we find that the size of the folded RNA structures, measured using the radius of gyration R-G, follows the Flory scaling law, namely, R-G=5.5N(1/3) angstrom, where N is the number of nucleotides. The shape of RNA molecules is characterized by the asphericity Delta and the shape S parameters that are computed using the eigenvalues of the moment of inertia tensor. From the distribution of Delta, we find that a large fraction of folded RNA structures are aspherical and the distribution of S values shows that RNA molecules are prolate (S > 0). The flexibility of folded structures is characterized by the persistence length l(p). By fitting the distance distribution function P(r), that is computed using the coordinates of the folded RNA, to the wormlike chain model we extracted the persistence length l(p). We find that l(p)approximate to 1.5N(0.33) angstrom which might reflect the large separation between the free energies that stabilize secondary and tertiary structures. The dependence of l(p) on N implies that the average length of helices should increase as the size of RNA grows. We also analyze packing in the structures of ribosomes (30S, 50S, and 70S) in terms of R-G, Delta, S, and l(p). The 70S and the 50S subunits are more spherical compared to most RNA molecules. The globularity in 50S is due to the presence of an unusually large number (compared to 30S subunit) of small helices that are stitched together by bulges and loops. Comparison of the shapes of the intact 70S ribosome and the constituent particles suggests that folding of the individual molecules might occur prior to assembly. (c) 2006 American Institute of Physics.
机译:确定RNA分子的大小和柔韧性对于理解折叠结构中的堆积性质以及阐明RNA与DNA或蛋白质之间的相互作用非常重要。使用蛋白质数据库中RNA的结构坐标,我们发现使用回转半径RG测得的折叠RNA结构的大小遵循弗洛里缩放定律,即RG = 5.5N(1/3)埃,其中N是核苷酸数。 RNA分子的形状由非球面度Delta和形状S参数表征,这些参数是使用惯性矩张量的特征值计算的。从Delta的分布中,我们发现大部分折叠的RNA结构是非球面的,S值的分布表明RNA分子呈扁长形(S> 0)。折叠结构的柔韧性由持久长度l(p)表征。通过将使用折叠RNA坐标计算出的距离分布函数P(r)拟合到蠕虫状链模型,我们提取了持久长度l(p)。我们发现l(p)大约为1.5N(0.33)埃,这可能反映了稳定二级结构和三级结构的自由能之间的较大间隔。 l(p)对N的依赖性意味着,螺旋的平均长度应随着RNA大小的增长而增加。我们还根据R-G,Delta,S和l(p)分析了核糖体(30S,50S和70S)结构中的堆积。与大多数RNA分子相比,70S和50S亚基更球形。 50S的球形性是由于存在小数目的异常(相对于30S亚基)的小螺旋,这些小螺旋通过凸起和环圈缝合在一起。比较完整的70S核糖体和组成颗粒的形状,表明单个分子的折叠可能在组装之前发生。 (c)2006年美国物理研究所。

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