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Visualizing large RNA molecules in solution.

机译:可视化溶液中的大RNA分子。

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Single-stranded RNAs (ssRNAs) longer than a few hundred nucleotides do not have a unique structure in solution. Their equilibrium properties therefore reflect the average of an ensemble of structures. We use cryo-electron microscopy to image projections of individual long ssRNA molecules and characterize the anisotropy of their ensembles in solution. A flattened prolate volume is found to best represent the shapes of these ensembles. The measured sizes and anisotropies are in good agreement with complementary determinations using small-angle X-ray scattering and coarse-grained molecular dynamics simulations. A long viral ssRNA is compared with shorter noncoding transcripts to demonstrate that prolate geometry and flatness are generic properties independent of sequence length and origin. The anisotropy persists under physiological as well as low-ionic-strength conditions, revealing a direct correlation between secondary structure asymmetry and 3D shape and size. We discuss the physical origin of the generic anisotropy and its biological implications.
机译:长于数百个核苷酸的单链RNA(ssRNA)在溶液中没有独特的结构。因此,它们的平衡特性反映了结构整体的平均值。我们使用冷冻电子显微镜对单个长ssRNA分子的图像进行成像,并表征它们在溶液中的集合体的各向异性。发现扁平的扁平体最能代表这些合奏的形状。所测量的尺寸和各向异性与使用小角度X射线散射和粗粒度分子动力学模拟进行的补充测定非常吻合。将较长的病毒ssRNA与较短的非编码转录本进行比较,以证明扁长的几何形状和平坦度是与序列长度和来源无关的通用属性。各向异性在生理以及低离子强度条件下均会持续存在,从而揭示了二级结构不对称性与3D形状和尺寸之间的直接关系。我们讨论了通用各向异性的物理起源及其生物学意义。

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