• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

FitEM2EM——用于大分子组装和动力学低分辨率研究的工具。

FitEM2EM--tools for low resolution study of macromolecular assembly and dynamics.

作者信息

Frankenstein Ziv, Sperling Joseph, Sperling Ruth, Eisenstein Miriam

机构信息

Department of Structural Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

PLoS One. 2008;3(10):e3594. doi: 10.1371/journal.pone.0003594. Epub 2008 Oct 31.

DOI:10.1371/journal.pone.0003594
PMID:18974836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2572833/
Abstract

Studies of the structure and dynamics of macromolecular assemblies often involve comparison of low resolution models obtained using different techniques such as electron microscopy or atomic force microscopy. We present new computational tools for comparing (matching) and docking of low resolution structures, based on shape complementarity. The matched or docked objects are represented by three dimensional grids where the value of each grid point depends on its position with regard to the interior, surface or exterior of the object. The grids are correlated using fast Fourier transformations producing either matches of related objects or docking models depending on the details of the grid representations. The procedures incorporate thickening and smoothing of the surfaces of the objects which effectively compensates for differences in the resolution of the matched/docked objects, circumventing the need for resolution modification. The presented matching tool FitEM2EMin successfully fitted electron microscopy structures obtained at different resolutions, different conformers of the same structure and partial structures, ranking correct matches at the top in every case. The differences between the grid representations of the matched objects can be used to study conformation differences or to characterize the size and shape of substructures. The presented low-to-low docking tool FitEM2EMout ranked the expected models at the top.

摘要

对大分子组装体的结构和动力学研究通常涉及对使用不同技术(如电子显微镜或原子力显微镜)获得的低分辨率模型进行比较。我们基于形状互补性,提出了用于比较(匹配)和对接低分辨率结构的新计算工具。匹配或对接的对象由三维网格表示,其中每个网格点的值取决于其相对于对象内部、表面或外部的位置。通过快速傅里叶变换对网格进行关联,根据网格表示的细节产生相关对象的匹配或对接模型。该程序包含对象表面的加厚和平滑处理,有效地补偿了匹配/对接对象分辨率的差异,避免了分辨率修改的需要。所提出的匹配工具FitEM2EMin成功地拟合了在不同分辨率、相同结构的不同构象和部分结构下获得的电子显微镜结构,在每种情况下都将正确的匹配排在首位。匹配对象的网格表示之间的差异可用于研究构象差异或表征子结构的大小和形状。所提出的低分辨率到低分辨率对接工具FitEM2EMout将预期模型排在首位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0751/2572833/4799c9635cc1/pone.0003594.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0751/2572833/15dc0e52c4fa/pone.0003594.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0751/2572833/4799c9635cc1/pone.0003594.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0751/2572833/15dc0e52c4fa/pone.0003594.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0751/2572833/4799c9635cc1/pone.0003594.g002.jpg

相似文献

1
FitEM2EM--tools for low resolution study of macromolecular assembly and dynamics.FitEM2EM——用于大分子组装和动力学低分辨率研究的工具。
PLoS One. 2008;3(10):e3594. doi: 10.1371/journal.pone.0003594. Epub 2008 Oct 31.
2
Shape complementarity of protein-protein complexes at multiple resolutions.多分辨率下蛋白质-蛋白质复合物的形状互补性。
Proteins. 2009 May 1;75(2):453-67. doi: 10.1002/prot.22256.
3
Macromolecular crowding: chemistry and physics meet biology (Ascona, Switzerland, 10-14 June 2012).大分子拥挤现象:化学与物理邂逅生物学(瑞士阿斯科纳,2012年6月10日至14日)
Phys Biol. 2013 Aug;10(4):040301. doi: 10.1088/1478-3975/10/4/040301. Epub 2013 Aug 2.
4
Multi-resolution anchor-point registration of biomolecular assemblies and their components.生物分子组装体及其组件的多分辨率锚点配准
J Struct Biol. 2007 Jan;157(1):271-80. doi: 10.1016/j.jsb.2006.08.008. Epub 2006 Aug 25.
5
An Efficient Low Storage and Memory Treatment of Gridded Interaction Fields for Simulations of Macromolecular Association.一种用于大分子缔合模拟的网格相互作用场的高效低存储和内存处理方法。
J Chem Theory Comput. 2016 Sep 13;12(9):4563-77. doi: 10.1021/acs.jctc.6b00350. Epub 2016 Aug 16.
6
Multi-resolution contour-based fitting of macromolecular structures.基于多分辨率轮廓的大分子结构拟合
J Mol Biol. 2002 Mar 29;317(3):375-84. doi: 10.1006/jmbi.2002.5438.
7
Protein-protein docking using 3D-Dock in rounds 3, 4, and 5 of CAPRI.在蛋白质-蛋白质相互作用预测技术评估(CAPRI)的第3、4和5轮中,使用3D-Dock进行蛋白质-蛋白质对接。
Proteins. 2005 Aug 1;60(2):281-8. doi: 10.1002/prot.20571.
8
Progress in protein-protein docking: atomic resolution predictions in the CAPRI experiment using RosettaDock with an improved treatment of side-chain flexibility.蛋白质-蛋白质对接的进展:在CAPRI实验中使用RosettaDock并改进侧链柔性处理实现原子分辨率预测。
Proteins. 2005 Aug 1;60(2):187-94. doi: 10.1002/prot.20556.
9
Hydrophobic complementarity in protein-protein docking.蛋白质-蛋白质对接中的疏水互补性。
Proteins. 2004 Jul 1;56(1):130-42. doi: 10.1002/prot.20145.
10
Generating triangulated macromolecular surfaces by Euclidean Distance Transform.通过欧几里得距离变换生成三角化大分子表面。
PLoS One. 2009 Dec 2;4(12):e8140. doi: 10.1371/journal.pone.0008140.

引用本文的文献

1
A unique spatial arrangement of the snRNPs within the native spliceosome emerges from in silico studies.来自于计算机模拟研究的结果表明,snRNPs 在天然剪接体中呈现独特的空间排列。
Structure. 2012 Jun 6;20(6):1097-106. doi: 10.1016/j.str.2012.03.022. Epub 2012 May 10.

本文引用的文献

1
Molecular electron microscopy: state of the art and current challenges.分子电子显微镜:现状与当前挑战
ACS Chem Biol. 2008 May 16;3(5):268-81. doi: 10.1021/cb800037d.
2
Near-atomic resolution using electron cryomicroscopy and single-particle reconstruction.使用电子冷冻显微镜和单颗粒重建技术实现近原子分辨率。
Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):1867-72. doi: 10.1073/pnas.0711623105. Epub 2008 Jan 31.
3
X-ray solution scattering (SAXS) combined with crystallography and computation: defining accurate macromolecular structures, conformations and assemblies in solution.
X射线溶液散射(SAXS)与晶体学和计算相结合:确定溶液中精确的大分子结构、构象和组装体。
Q Rev Biophys. 2007 Aug;40(3):191-285. doi: 10.1017/S0033583507004635.
4
Structures of modified eEF2 80S ribosome complexes reveal the role of GTP hydrolysis in translocation.修饰后的真核延伸因子2(eEF2)80S核糖体复合物结构揭示了GTP水解在转位过程中的作用。
EMBO J. 2007 May 2;26(9):2421-31. doi: 10.1038/sj.emboj.7601677. Epub 2007 Apr 19.
5
From high-resolution AFM topographs to atomic models of supramolecular assemblies.从高分辨率原子力显微镜形貌图到超分子组装体的原子模型。
J Struct Biol. 2007 Aug;159(2):268-76. doi: 10.1016/j.jsb.2007.01.021. Epub 2007 Feb 17.
6
Reconfiguration of yeast 40S ribosomal subunit domains by the translation initiation multifactor complex.翻译起始多因子复合物对酵母40S核糖体亚基结构域的重新配置。
Proc Natl Acad Sci U S A. 2007 Apr 3;104(14):5788-93. doi: 10.1073/pnas.0606880104. Epub 2007 Mar 26.
7
Visualizing the ATPase cycle in a protein disaggregating machine: structural basis for substrate binding by ClpB.在蛋白质解聚机器中可视化ATP酶循环:ClpB结合底物的结构基础。
Mol Cell. 2007 Jan 26;25(2):261-71. doi: 10.1016/j.molcel.2007.01.002.
8
Visualizing flexibility at molecular resolution: analysis of heterogeneity in single-particle electron microscopy reconstructions.在分子分辨率下可视化灵活性:单颗粒电子显微镜重建中的异质性分析。
Annu Rev Biophys Biomol Struct. 2007;36:43-62. doi: 10.1146/annurev.biophys.36.040306.132742.
9
Dodecameric structure and ATPase activity of the human TIP48/TIP49 complex.人TIP48/TIP49复合物的十二聚体结构及ATP酶活性
J Mol Biol. 2007 Feb 9;366(1):179-92. doi: 10.1016/j.jmb.2006.11.030. Epub 2006 Nov 11.
10
An expanded conformation of single-ring GroEL-GroES complex encapsulates an 86 kDa substrate.单环GroEL-GroES复合物的扩展构象包裹着一个86 kDa的底物。
Structure. 2006 Nov;14(11):1711-22. doi: 10.1016/j.str.2006.09.010.