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蛋白质结构网络的优化空模型

Optimized null model for protein structure networks.

作者信息

Milenković Tijana, Filippis Ioannis, Lappe Michael, Przulj Natasa

机构信息

Department of Computer Science, University of California Irvine, Irvine, CA, USA.

出版信息

PLoS One. 2009 Jun 26;4(6):e5967. doi: 10.1371/journal.pone.0005967.

Abstract

Much attention has recently been given to the statistical significance of topological features observed in biological networks. Here, we consider residue interaction graphs (RIGs) as network representations of protein structures with residues as nodes and inter-residue interactions as edges. Degree-preserving randomized models have been widely used for this purpose in biomolecular networks. However, such a single summary statistic of a network may not be detailed enough to capture the complex topological characteristics of protein structures and their network counterparts. Here, we investigate a variety of topological properties of RIGs to find a well fitting network null model for them. The RIGs are derived from a structurally diverse protein data set at various distance cut-offs and for different groups of interacting atoms. We compare the network structure of RIGs to several random graph models. We show that 3-dimensional geometric random graphs, that model spatial relationships between objects, provide the best fit to RIGs. We investigate the relationship between the strength of the fit and various protein structural features. We show that the fit depends on protein size, structural class, and thermostability, but not on quaternary structure. We apply our model to the identification of significantly over-represented structural building blocks, i.e., network motifs, in protein structure networks. As expected, choosing geometric graphs as a null model results in the most specific identification of motifs. Our geometric random graph model may facilitate further graph-based studies of protein conformation space and have important implications for protein structure comparison and prediction. The choice of a well-fitting null model is crucial for finding structural motifs that play an important role in protein folding, stability and function. To our knowledge, this is the first study that addresses the challenge of finding an optimized null model for RIGs, by comparing various RIG definitions against a series of network models.

摘要

最近,生物网络中观察到的拓扑特征的统计显著性受到了广泛关注。在这里,我们将残基相互作用图(RIGs)视为蛋白质结构的网络表示,其中残基为节点,残基间相互作用为边。度保持随机化模型已广泛用于生物分子网络的这一目的。然而,网络的这种单一汇总统计量可能不够详细,无法捕捉蛋白质结构及其网络对应物的复杂拓扑特征。在这里,我们研究了RIGs的各种拓扑性质,以找到适合它们的网络空模型。RIGs来自不同距离截止值和不同相互作用原子组的结构多样的蛋白质数据集。我们将RIGs的网络结构与几种随机图模型进行比较。我们表明,模拟对象间空间关系的三维几何随机图最适合RIGs。我们研究了拟合强度与各种蛋白质结构特征之间的关系。我们表明,拟合取决于蛋白质大小、结构类别和热稳定性,但不取决于四级结构。我们将我们的模型应用于识别蛋白质结构网络中显著过度代表的结构构建块,即网络基序。正如预期的那样,选择几何图作为空模型会导致对基序的最具体识别。我们的几何随机图模型可能有助于进一步基于图的蛋白质构象空间研究,并对蛋白质结构比较和预测具有重要意义。选择合适的空模型对于找到在蛋白质折叠、稳定性和功能中起重要作用的结构基序至关重要。据我们所知,这是第一项通过将各种RIG定义与一系列网络模型进行比较来应对为RIGs找到优化空模型这一挑战的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2ed/2699654/8c15c3fbd5a5/pone.0005967.g001.jpg

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