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一种用于预测动物膜蛋白功能类型的多标签分类器。

A multi-label classifier for prediction membrane protein functional types in animal.

作者信息

Zou Hong-Liang

机构信息

Computer Department, Jing-De-Zhen Ceramic Institute, Jing-De-Zhen, 333046, China,

出版信息

J Membr Biol. 2014 Nov;247(11):1141-8. doi: 10.1007/s00232-014-9708-2. Epub 2014 Aug 9.

Abstract

Membrane protein is an important composition of cell membrane. Given a membrane protein sequence, how can we identify its type(s) is very important because the type keeps a close correlation with its functions. According to previous studies, membrane protein can be divided into the following eight types: single-pass type I, single-pass type II, single-pass type III, single-pass type IV, multipass, lipid-anchor, GPI-anchor, peripheral membrane protein. With the avalanche of newly found protein sequences in the post-genomic age, it is urgent to develop an automatic and effective computational method to rapid and reliable prediction of the types of membrane proteins. At present, most of the existing methods were based on the assumption that one membrane protein only belongs to one type. Actually, a membrane protein may simultaneously exist at two or more different functional types. In this study, a new method by hybridizing the pseudo amino acid composition with multi-label algorithm called LIFT (multi-label learning with label-specific features) was proposed to predict the functional types both singleplex and multiplex animal membrane proteins. Experimental result on a stringent benchmark dataset of membrane proteins by jackknife test show that the absolute-true obtained was 0.6342, indicating that our approach is quite promising. It may become a useful high-through tool, or at least play a complementary role to the existing predictors in identifying functional types of membrane proteins.

摘要

膜蛋白是细胞膜的重要组成部分。给定一段膜蛋白序列,如何识别其类型非常重要,因为类型与其功能密切相关。根据以往的研究,膜蛋白可分为以下八种类型:单次跨膜I型、单次跨膜II型、单次跨膜III型、单次跨膜IV型、多次跨膜、脂锚定、糖基磷脂酰肌醇锚定、外周膜蛋白。在后基因组时代,随着新发现的蛋白质序列大量涌现,迫切需要开发一种自动有效的计算方法,以便快速可靠地预测膜蛋白的类型。目前,大多数现有方法基于一种膜蛋白只属于一种类型的假设。实际上,一种膜蛋白可能同时存在于两种或更多不同的功能类型中。在本研究中,提出了一种将伪氨基酸组成与称为LIFT(基于标签特定特征的多标签学习)的多标签算法相结合的新方法,用于预测单重和多重动物膜蛋白的功能类型。通过留一法测试在一个严格的膜蛋白基准数据集上的实验结果表明,获得的绝对真值为0.6342,这表明我们的方法很有前景。它可能成为一种有用的高通量工具,或者至少在识别膜蛋白功能类型方面对现有预测器起到补充作用。

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