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A regularized discriminative model for the prediction of protein-peptide interactions

机译:预测蛋白质-肽相互作用的正则化判别模型

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Motivation: Short well-defined domains known as peptide recognition modules (PRMs) regulate many important protein-protein interactions involved in the formation of macromolecular complexes and biochemical pathways. Since high-throughput experiments like yeast two-hybrid and phage display are expensive and intrinsically noisy, it would be desirable to more specifically target or partially bypass them with complementary in silico approaches. In the present paper, we present a probabilistic discriminative approach to predicting PRM-mediated protein-protein interactions from sequence data. The model is motivated by the discriminative model of Segal and Sharan as an alternative to the generative approach of Reiss and Schwikowski. In our evaluation, we focus on predicting the interaction network. As proposed by Williams, we overcome the problem of susceptibility to over-fitting by adopting a Bayesian a posteriori approach based on a Laplacian prior in parameter space.
机译:动机:短的明确定义的域,称为肽识别模块(PRM),调节与大分子复合物的形成和生化途径有关的许多重要的蛋白质-蛋白质相互作用。由于高通量实验(如酵母双杂交和噬菌体展示)既昂贵又固有噪声,因此希望使用互补的计算机方法更具体地靶向或部分绕过它们。在本文中,我们提出了一种概率判别方法,可从序列数据预测PRM介导的蛋白质-蛋白质相互作用。该模型是由Segal和Sharan的判别模型驱动的,是Reiss和Schwikowski生成方法的替代方法。在我们的评估中,我们专注于预测交互网络。正如威廉姆斯所提出的,我们通过在参数空间中采用基于拉普拉斯先验的贝叶斯后验方法克服了过度拟合的易感性问题。

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