Ambiguity assessment of small-angle scattering curves from monodisperse systems.

Maxim V Petoukhov, Dmitri I Svergun
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引用次数: 101

Abstract

A novel approach is presented for an a priori assessment of the ambiguity associated with spherically averaged single-particle scattering. The approach is of broad interest to the structural biology community, allowing the rapid and model-independent assessment of the inherent non-uniqueness of three-dimensional shape reconstruction from scattering experiments on solutions of biological macromolecules. One-dimensional scattering curves recorded from monodisperse systems are nowadays routinely utilized to generate low-resolution particle shapes, but the potential ambiguity of such reconstructions remains a major issue. At present, the (non)uniqueness can only be assessed by a posteriori comparison and averaging of repetitive Monte Carlo-based shape-determination runs. The new a priori ambiguity measure is based on the number of distinct shape categories compatible with a given data set. For this purpose, a comprehensive library of over 14,000 shape topologies has been generated containing up to seven beads closely packed on a hexagonal grid. The computed scattering curves rescaled to keep only the shape topology rather than the overall size information provide a `scattering map' of this set of shapes. For a given scattering data set, one rapidly obtains the number of neighbours in the map and the associated shape topologies such that in addition to providing a quantitative ambiguity measure the algorithm may also serve as an alternative shape-analysis tool. The approach has been validated in model calculations on geometrical bodies and its usefulness is further demonstrated on a number of experimental X-ray scattering data sets from proteins in solution. A quantitative ambiguity score (a-score) is introduced to provide immediate and convenient guidance to the user on the uniqueness of the ab initio shape reconstruction from the given data set.

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单分散系统小角度散射曲线的模糊性评价。
提出了一种新的方法来先验地评估与球平均单粒子散射相关的模糊性。该方法引起了结构生物学界的广泛兴趣,允许对生物大分子溶液散射实验中三维形状重建的固有非唯一性进行快速和模型独立的评估。单分散系统记录的一维散射曲线目前通常用于生成低分辨率粒子形状,但这种重建的潜在模糊性仍然是一个主要问题。目前,(非)唯一性只能通过后验比较和基于蒙特卡罗的重复形状确定运行的平均来评估。新的先验模糊度量是基于与给定数据集兼容的不同形状类别的数量。为此,一个包含超过14,000个形状拓扑的综合库已经生成,其中包含多达七个紧密排列在六边形网格上的珠子。计算的散射曲线被重新缩放,只保留形状拓扑而不是整体尺寸信息,从而提供了这组形状的“散射图”。对于给定的散射数据集,可以快速获得地图中邻居的数量和相关的形状拓扑,这样除了提供定量模糊度量外,该算法还可以作为替代的形状分析工具。该方法已在几何物体的模型计算中得到验证,并在溶液中蛋白质的一些实验x射线散射数据集上进一步证明了其有效性。引入定量模糊评分(A -score),为用户从给定数据集从头开始形状重建的唯一性提供直接和方便的指导。
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