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Novel convergence-oriented approach for evaluation and optimization of workflow in single-particle two-dimensional averaging of electron microscope images

机译:电子显微镜图像单粒子二维平均中评估和优化工作流的面向收敛的新方法

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Three-dimensional (3D) protein structures facilitate the understanding of their biological functions and provide valuable information for developing medicines. Single-particle analysis (SPA) from electron microscopy (EM) is a structure determination method suitable for macromolecules. To achieve a high resolution using combinations of several SPA software packages, 'workflow' optimization and comparative evaluation by scoring results are essential. Two-dimensional (2D) averaging is a key step for 3D reconstruction. The integrated convergence-evaluation oriented system (IC-EOS) proposed here provides an effective tool for customizing 2D averaging. This assesses the behavior and characteristics of workflows and evaluates the convergence of iteration steps without human intervention. We chose five base measurements for quantifying convergence: resolution, variance, similarity, shift-distance and rotation-angle. Curve fitting to history graphs scored their stability. We call this score 'fluctuation'. The number of particle images discarded from the library and the number of classification groups were examined to see their effects on optimization levels and fluctuation of measurements, allowing the IC-EOS to select the most appropriate workflow for the target. A case study using a bacterial sodium channel and a simulation study using GroEL showed that resolution of 2D averaging improved with relatively stricter particle selection. With fewer groups, resolutions of class averages improved, but similarities between class-averages and their constituent particle images degraded. Fluctuation was useful for selecting adequate conditions, even when achieved values alone were not conclusive. The vote method, using fluctuation, was robust against noise and enabled a decision without exhaustive search trials. Thus, the,JC-EOS is a step toward full automation of SPA.
机译:三维(3D)蛋白质结构有助于理解其生物学功能,并为开发药物提供有价值的信息。电子显微镜(EM)的单颗粒分析(SPA)是适用于大分子的结构确定方法。为了使用多个SPA软件包的组合获得高分辨率,通过评分结果进行“工作流程”优化和比较评估至关重要。二维(2D)平均是3D重建的关键步骤。此处提出的集成的面向收敛评估的系统(IC-EOS)为定制2D平均提供了有效的工具。这将评估工作流的行为和特征,并评估迭代步骤的收敛性,而无需人工干预。我们选择了五个用于量化收敛的基本度量:分辨率,方差,相似度,移位距离和旋转角度。曲线拟合历史图记录了其稳定性。我们称此分数为“波动”。检查了从库中丢弃的粒子图像的数量和分类组的数量,以查看它们对优化级别和测量波动的影响,从而使IC-EOS可以为目标选择最合适的工作流程。使用细菌钠通道进行的案例研究和使用GroEL进行的模拟研究表明,通过相对严格的粒子选择,可以提高2D平均分辨率。随着组的减少,类平均的分辨率得到改善,但是类平均与其组成的粒子图像之间的相似性降低了。波动对于选择适当的条件很有用,即使仅达到的值尚无定论。使用波动的表决方法具有很强的抗噪能力,并且可以进行详尽的搜索试验。因此,JC-EOS是朝着SPA完全自动化迈出的一步。

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