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本文引用的文献

1
Modularity analysis based on predicted protein-protein interactions provides new insights into pathogenicity and cellular process of Escherichia coli O157:H7.基于预测的蛋白质-蛋白质相互作用的模块性分析为大肠杆菌O157:H7的致病性和细胞过程提供了新的见解。
Theor Biol Med Model. 2011 Dec 22;8:47. doi: 10.1186/1742-4682-8-47.
2
Predicting protein-protein interactions from protein domains using a set cover approach.使用集合覆盖方法从蛋白质结构域预测蛋白质-蛋白质相互作用。
IEEE/ACM Trans Comput Biol Bioinform. 2007 Jan-Mar;4(1):78-87. doi: 10.1109/TCBB.2007.1001.
3
Evaluation of clustering algorithms for protein-protein interaction networks.蛋白质-蛋白质相互作用网络聚类算法的评估
BMC Bioinformatics. 2006 Nov 6;7:488. doi: 10.1186/1471-2105-7-488.
4
Global landscape of protein complexes in the yeast Saccharomyces cerevisiae.酿酒酵母中蛋白质复合物的全球格局。
Nature. 2006 Mar 30;440(7084):637-43. doi: 10.1038/nature04670. Epub 2006 Mar 22.
5
Proteome survey reveals modularity of the yeast cell machinery.蛋白质组研究揭示酵母细胞机制的模块化特性。
Nature. 2006 Mar 30;440(7084):631-6. doi: 10.1038/nature04532. Epub 2006 Jan 22.
6
Protein interaction networks of Saccharomyces cerevisiae, Caenorhabditis elegans and Drosophila melanogaster: large-scale organization and robustness.酿酒酵母、秀丽隐杆线虫和黑腹果蝇的蛋白质相互作用网络:大规模组织与稳健性
Proteomics. 2006 Jan;6(2):456-61. doi: 10.1002/pmic.200500228.
7
Functional and topological characterization of protein interaction networks.蛋白质相互作用网络的功能与拓扑特征
Proteomics. 2004 Apr;4(4):928-42. doi: 10.1002/pmic.200300636.
8
Inferring domain-domain interactions from protein-protein interactions.从蛋白质-蛋白质相互作用推断结构域-结构域相互作用。
Genome Res. 2002 Oct;12(10):1540-8. doi: 10.1101/gr.153002.
9
Hierarchical organization of modularity in metabolic networks.代谢网络中模块化的层次组织。
Science. 2002 Aug 30;297(5586):1551-5. doi: 10.1126/science.1073374.
10
Complete genome sequence of enterohemorrhagic Escherichia coli O157:H7 and genomic comparison with a laboratory strain K-12.肠出血性大肠杆菌O157:H7全基因组序列及与实验室菌株K-12的基因组比较
DNA Res. 2001 Feb 28;8(1):11-22. doi: 10.1093/dnares/8.1.11.

基于 PPI 网络的模块性分析应用于测序生物。

Applying modularity analysis of PPI networks to sequenced organisms.

机构信息

Beijing Institute of Biotechnology, Beijing, China.

出版信息

Virulence. 2012 Aug 15;3(5):459-63. doi: 10.4161/viru.21104.

DOI:10.4161/viru.21104
PMID:23076246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3485987/
Abstract

The interaction between proteins is one of the most important features of protein functions. In general, the protein-protein interactions (PPIs) network of an organism is very complex, consisting of huge amount of PPIs. Functional modules can be identified from the complex protein interaction networks. It follows that the investigation of functional modules will generate a better understanding of cellular organization, processes and functions. However, it is a great challenge to apply modularity analysis to under-studied organism, even though this organism has already been sequenced, as there are few or none experimental validated PPI data for them. Therefore, by integrating several bioinformatics methods, we provide a solution for modularity analysis of any sequenced organism. By this way, new information may be found for the organism in different level, such as protein-protein interaction, pathways or cellular process. For the computation part, it takes one to two weeks. The main impact factors are computer power and size of the PPI network. It takes longer time for the manually analysis of biological meanings of the modules.

摘要

蛋白质之间的相互作用是蛋白质功能的最重要特征之一。一般来说,生物体的蛋白质-蛋白质相互作用(PPI)网络非常复杂,包含大量的 PPI。可以从复杂的蛋白质互作网络中识别功能模块。因此,对功能模块的研究将更好地理解细胞的组织、过程和功能。然而,即使对于已经测序的生物体,应用模块性分析也是一个巨大的挑战,因为它们几乎没有或根本没有经过实验验证的 PPI 数据。因此,我们通过整合几种生物信息学方法,为任何已测序的生物体的模块性分析提供了一种解决方案。通过这种方式,可以在不同的层次上为生物体找到新的信息,例如蛋白质-蛋白质相互作用、途径或细胞过程。对于计算部分,需要一到两周的时间。主要的影响因素是计算机的能力和 PPI 网络的大小。模块的生物学意义的人工分析需要更长的时间。