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膜蛋白管状晶体的结构测定。IV. 畸变校正及其与实空间平均和溶剂扁平化的联合应用。

Structure determination of tubular crystals of membrane proteins. IV. Distortion correction and its combined application with real-space averaging and solvent flattening.

作者信息

Yonekura Koji, Toyoshima Chikashi

机构信息

The W.M. Keck Advanced Microscopy Laboratory, Department of Biochemistry and Biophysics, University of California, San Francisco, 1700, 4th Street San Francisco, CA 94158-2532, USA.

出版信息

Ultramicroscopy. 2007 Nov;107(12):1141-58. doi: 10.1016/j.ultramic.2007.01.013. Epub 2007 Feb 14.

Abstract

A method for correction of three-dimensional distortions has been developed for helical assemblies and applied to tubular crystals of Ca2+-ATPase. This method approximates distorted helical particles with short straight segments of different orientation parameters, which are determined by fitting them to the reference data in reciprocal space. Thus, the method follows Beroukhim and Unwin [Ultramicroscopy 70 (1997) 57], but is more extended to achieve better alignment and to cope with images of poor S/N ratio. Substantial improvements were achieved by dividing the reference image into the segments of optimal lengths in exactly the same way as the test, and treating the distortions in the near and far sides of a helical particle separately. The improvement was further enhanced when combined with real-space averaging [Yonekura, Toyoshima, Ultramicroscopy 84 (2000) 15] and solvent flattening [Yonekura, Toyoshima, Ultramicroscopy 84 (2000) 29], and most pronounced when all these three were applied iteratively.

摘要

一种用于校正螺旋组件三维畸变的方法已被开发出来,并应用于Ca2+-ATP酶的管状晶体。该方法用具有不同取向参数的短直线段来近似畸变的螺旋颗粒,这些参数通过将它们拟合到倒易空间中的参考数据来确定。因此,该方法沿用了贝鲁希姆和昂温[《超微结构》70 (1997) 57]的方法,但进行了更扩展,以实现更好的对齐并处理信噪比低的图像。通过以与测试完全相同的方式将参考图像划分为最佳长度的段,并分别处理螺旋颗粒近侧和远侧的畸变,取得了显著的改进。当与实空间平均[米仓、丰岛,《超微结构》84 (2000) 15]和溶剂扁平化[米仓、丰岛,《超微结构》84 (2000) 29]相结合时,改进进一步增强,当这三者迭代应用时最为明显。

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