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通过几种二级结构预测方法对跨膜β链预测进行严格评估后,对布鲁氏菌流产亚种孔蛋白Omp2b和Omp2a进行拓扑预测。

Topology prediction of Brucella abortus Omp2b and Omp2a porins after critical assessment of transmembrane beta strands prediction by several secondary structure prediction methods.

作者信息

Paquet J Y, Vinals C, Wouters J, Letesson J J, Depiereux E

机构信息

Unité de Recherche en Biologie Moléculaire, Facultés Universitaires Notre-Dame-de-la-Paix, Namur, Belgium.

出版信息

J Biomol Struct Dyn. 2000 Feb;17(4):747-57. doi: 10.1080/07391102.2000.10506564.

DOI:10.1080/07391102.2000.10506564
PMID:10698111
Abstract

In order to propose a reliable model for Brucella porin topology, several structure prediction methods were evaluated in their ability to predict porin topology. Four porins of known structure were selected as test-cases and their secondary structure delineated. The specificity and sensitivity of 11 methods were separately evaluated. Our critical assessment shows that some secondary structure prediction methods (PHD, Dsc, Sopma) originally designed to predict globular protein structure are useful on porin topology prediction. The overall best prediction is obtained by combining these three "generalist" methods with a transmembrane beta strand prediction technique. This "consensus" method was applied to Brucella porins Omp2b and Omp2a, sharing no sequence homology with any other porin. The predicted topology is a 16-stranded antiparallel beta barrel with Omp2a showing a higher number of negatively charged residue in the exposed loops than Omp2b. Experiments are in progress to validate the proposed topology and the functional hypotheses. The ability of the proposed consensus method to predict topology of complex outer membrane protein is briefly discussed.

摘要

为了提出一种可靠的布鲁氏菌孔蛋白拓扑结构模型,对几种结构预测方法预测孔蛋白拓扑结构的能力进行了评估。选择了四种已知结构的孔蛋白作为测试案例,并确定了它们的二级结构。分别评估了11种方法的特异性和敏感性。我们的批判性评估表明,一些最初设计用于预测球状蛋白质结构的二级结构预测方法(PHD、Dsc、Sopma)在孔蛋白拓扑结构预测中很有用。通过将这三种“通用”方法与跨膜β链预测技术相结合,获得了总体最佳预测。这种“共识”方法应用于与其他任何孔蛋白均无序列同源性的布鲁氏菌孔蛋白Omp2b和Omp2a。预测的拓扑结构是一个16链反平行β桶,Omp2a在暴露环中显示出比Omp2b更多的带负电荷残基。正在进行实验以验证所提出的拓扑结构和功能假设。简要讨论了所提出的共识方法预测复杂外膜蛋白拓扑结构的能力。

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