从旋转平均二维x射线衍射图恢复昆虫飞行肌肉的三维结构。

IF 3.8 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Hiroyuki Iwamoto
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引用次数: 0

摘要

肌肉的收缩机制,特别是骨骼肌的收缩机制,具有非常规则的收缩蛋白细丝排列,并在x射线照射时产生复杂而有信息的衍射图案。然而,分析这些衍射模式往往具有挑战性,因为(i)只能获得旋转平均衍射模式,导致大量信息丢失,(ii)收缩机制包含两组不同的蛋白质细丝(肌动蛋白和肌球蛋白),具有不同的螺旋对称性。它们发出的反射经常重叠。如果直接从衍射图样中计算出可收缩机械的实空间三维结构,就可以解决这些问题。在这里,我们证明了使用传统的相位检索算法(混合输入-输出),可以有效地从单个旋转平均二维衍射图中恢复收缩机械的真实空间三维结构。在这个计算中,我们使用了一个昆虫飞行肌肉的计算机模型,它以其高度规则的结构而闻名。我们还将这种技术扩展到实验记录的肌肉衍射模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Restoration of the 3D structure of insect flight muscle from a rotationally averaged 2D X-ray diffraction pattern.

The contractile machinery of muscle, especially that of skeletal muscle, has a very regular array of contractile protein filaments, and gives rise to a complex and informative diffraction pattern when irradiated with X-rays. However, analyzing these diffraction patterns is often challenging because (i) only rotationally averaged diffraction patterns can be obtained, resulting in a substantial loss of information, and (ii) the contractile machinery contains two different sets of protein filaments (actin and myosin) with different helical symmetries. The reflections originating from them often overlap. These problems may be solved if the real-space 3D structure of the contractile machinery is directly calculated from the diffraction pattern. Here, we demonstrate that by using the conventional phase-retrieval algorithm (hybrid input-output), the real-space 3D structure of the contractile machinery can be effectively restored from a single rotationally averaged 2D diffraction pattern. In this calculation, we used an in silico model of insect flight muscle, which is known for its highly regular structure. We also extended this technique to an experimentally recorded muscle diffraction pattern.

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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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