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RNA标准原子体积的计算及其与蛋白质的比较:RNA的堆积更为紧密。

Calculation of standard atomic volumes for RNA and comparison with proteins: RNA is packed more tightly.

作者信息

Voss N R, Gerstein M

机构信息

Molecular Biophysics and Biochemistry, Yale University, 260 Whitney Ave, P.O. Box 208114, New Haven, CT 06520, USA.

出版信息

J Mol Biol. 2005 Feb 18;346(2):477-92. doi: 10.1016/j.jmb.2004.11.072. Epub 2005 Jan 5.

Abstract

Traditionally, for biomolecular packing calculations research has focused on proteins. Besides proteins, RNA is the other large biomolecule that has tertiary structure interactions and complex packing. No one has yet quantitatively investigated RNA packing or compared its packing to that of proteins because, until recently, there were no large RNA structures. Here we address this question in detail, using Voronoi volume calculations on a set of high-resolution RNA crystal structures. We do a careful parameterization, taking into account many factors such as atomic radii, crystal packing, structural complexity, solvent, and associated protein to obtain a self-consistent, universal set of volumes that can be applied to both RNA and protein. We report this set of volumes, which we call the NucProt parameter set. Our measured values are consistent across the many different RNA structures and packing environments. When common atom types are compared between proteins and RNA, nine of 12 types show that RNA has a smaller volume and packs more tightly than protein, suggesting that close-packing may be as important for the folding of RNAs as it is for proteins. Moreover, calculated partial specific volumes show that RNA bases pack more densely than corresponding aromatic residues from proteins. Finally, we find that RNA bases have similar packing volumes to DNA bases, despite the absence of tertiary contacts in DNA. Programs, parameter sets and raw data are available online at.

摘要

传统上,在生物分子堆积计算方面,研究主要集中在蛋白质上。除了蛋白质,RNA是另一种具有三级结构相互作用和复杂堆积的大型生物分子。由于直到最近还没有大型RNA结构,所以还没有人对RNA堆积进行定量研究,也没有人将其堆积情况与蛋白质的进行比较。在这里,我们使用一组高分辨率RNA晶体结构的Voronoi体积计算来详细解决这个问题。我们进行了仔细的参数化,考虑了许多因素,如原子半径、晶体堆积、结构复杂性、溶剂和相关蛋白质,以获得一组自洽的、通用的体积值,该体积值可同时应用于RNA和蛋白质。我们报告了这组体积值,我们称之为NucProt参数集。我们的测量值在许多不同的RNA结构和堆积环境中都是一致的。当比较蛋白质和RNA之间的常见原子类型时,12种类型中的9种表明RNA的体积更小,堆积比蛋白质更紧密,这表明紧密堆积对于RNA折叠可能与蛋白质折叠同样重要。此外,计算得到的偏比容表明RNA碱基比蛋白质中的相应芳香族残基堆积更密集。最后,我们发现尽管DNA中不存在三级接触,但RNA碱基的堆积体积与DNA碱基相似。程序、参数集和原始数据可在网上获取。

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