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2
Evolutionary tabu search strategies for the simultaneous registration of multiple atomic structures in cryo-EM reconstructions.用于低温电子显微镜重构中多个原子结构同时配准的进化禁忌搜索策略。
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3
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Combine Cryo-EM Density Map and Residue Contact for Protein Structure Prediction - A Case Study.结合冷冻电镜密度图和残基接触进行蛋白质结构预测——一个案例研究。
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Analysis of β-strand Twist from the 3-dimensional Image of a Protein.从蛋白质三维图像分析β链扭曲
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Exploratory Studies Detecting Secondary Structures in Medium Resolution 3D Cryo-EM Images Using Deep Convolutional Neural Networks.使用深度卷积神经网络在中等分辨率3D冷冻电镜图像中检测二级结构的探索性研究。
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本文引用的文献

1
Using Sculptor and Situs for simultaneous assembly of atomic components into low-resolution shapes.利用 Sculptor 和 Situs 同时将原子组件组装成低分辨率的形状。
J Struct Biol. 2011 Mar;173(3):428-35. doi: 10.1016/j.jsb.2010.11.002. Epub 2010 Nov 13.
2
Single particle analysis at high resolution.高分辨率单颗粒分析
Methods Enzymol. 2010;482:211-35. doi: 10.1016/S0076-6879(10)82009-9.
3
Evolutionary tabu search strategies for the simultaneous registration of multiple atomic structures in cryo-EM reconstructions.用于低温电子显微镜重构中多个原子结构同时配准的进化禁忌搜索策略。
J Struct Biol. 2010 Apr;170(1):164-71. doi: 10.1016/j.jsb.2009.12.028. Epub 2010 Jan 7.
4
EM-fold: De novo folding of alpha-helical proteins guided by intermediate-resolution electron microscopy density maps.EM-fold:由中等分辨率电子显微镜密度图引导的α-螺旋蛋白从头折叠
Structure. 2009 Jul 15;17(7):990-1003. doi: 10.1016/j.str.2009.06.001.
5
Mechanism of gate opening in the 20S proteasome by the proteasomal ATPases.蛋白酶体ATP酶介导20S蛋白酶体门控开放的机制
Mol Cell. 2008 May 9;30(3):360-8. doi: 10.1016/j.molcel.2008.03.004.
6
The Jpred 3 secondary structure prediction server.Jpred 3二级结构预测服务器。
Nucleic Acids Res. 2008 Jul 1;36(Web Server issue):W197-201. doi: 10.1093/nar/gkn238. Epub 2008 May 7.
7
De novo backbone trace of GroEL from single particle electron cryomicroscopy.基于单颗粒电子冷冻显微镜技术的GroEL从头构建主链轨迹
Structure. 2008 Mar;16(3):441-8. doi: 10.1016/j.str.2008.02.007.
8
Averaging tens to hundreds of icosahedral particle images to resolve protein secondary structure elements using a Multi-Path Simulated Annealing optimization algorithm.使用多路径模拟退火优化算法对数十到数百个二十面体颗粒图像进行平均,以解析蛋白质二级结构元件。
J Struct Biol. 2007 Oct;160(1):11-27. doi: 10.1016/j.jsb.2007.06.009. Epub 2007 Jul 6.
9
Computational prediction of atomic structures of helical membrane proteins aided by EM maps.借助电子显微镜图谱辅助的螺旋膜蛋白原子结构的计算预测。
Biophys J. 2007 Sep 15;93(6):1950-9. doi: 10.1529/biophysj.106.102137. Epub 2007 May 11.
10
The beginning of kinesin's force-generating cycle visualized at 9-A resolution.以9埃分辨率观察到驱动蛋白力产生循环的起始阶段。
J Cell Biol. 2007 May 7;177(3):377-85. doi: 10.1083/jcb.200612090. Epub 2007 Apr 30.

在低温电子显微镜重构中追踪α螺旋的进化双向扩展。

Evolutionary bidirectional expansion for the tracing of alpha helices in cryo-electron microscopy reconstructions.

机构信息

School of Biomedical Informatics, The University of Texas Health Science Center at Houston, 7000 Fannin St., Houston, TX 77030, USA.

出版信息

J Struct Biol. 2012 Feb;177(2):410-9. doi: 10.1016/j.jsb.2011.11.029. Epub 2011 Dec 6.

DOI:10.1016/j.jsb.2011.11.029
PMID:22155667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3288247/
Abstract

Cryo-electron microscopy (cryo-EM) enables the imaging of macromolecular complexes in near-native environments at resolutions that often permit the visualization of secondary structure elements. For example, alpha helices frequently show consistent patterns in volumetric maps, exhibiting rod-like structures of high density. Here, we introduce VolTrac (Volume Tracer) - a novel technique for the annotation of alpha-helical density in cryo-EM data sets. VolTrac combines a genetic algorithm and a bidirectional expansion with a tabu search strategy to trace helical regions. Our method takes advantage of the stochastic search by using a genetic algorithm to identify optimal placements for a short cylindrical template, avoiding exploration of already characterized tabu regions. These placements are then utilized as starting positions for the adaptive bidirectional expansion that characterizes the curvature and length of the helical region. The method reliably predicted helices with seven or more residues in experimental and simulated maps at intermediate (4-10Å) resolution. The observed success rates, ranging from 70.6% to 100%, depended on the map resolution and validation parameters. For successful predictions, the helical axes were located within 2Å from known helical axes of atomic structures.

摘要

冷冻电子显微镜(cryo-EM)能够在接近天然环境的条件下对大分子复合物进行成像,其分辨率通常可以允许观察到二级结构元件。例如,α螺旋通常在体绘制图中呈现出一致的模式,表现出高密度的棒状结构。在这里,我们引入了 VolTrac(Volume Tracer)——一种用于冷冻电镜数据集α螺旋密度注释的新技术。VolTrac 结合了遗传算法和双向扩展以及禁忌搜索策略来跟踪螺旋区域。我们的方法利用遗传算法的随机搜索来识别短圆柱模板的最佳位置,避免探索已经确定的禁忌区域。然后,这些位置被用作自适应双向扩展的起始位置,该扩展用于描述螺旋区域的曲率和长度。该方法在中间(4-10Å)分辨率的实验和模拟图谱中可靠地预测了具有七个或更多残基的螺旋。观察到的成功率从 70.6%到 100%不等,这取决于图谱分辨率和验证参数。对于成功的预测,螺旋轴与原子结构的已知螺旋轴之间的距离在 2Å 以内。