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Prediction-based fingerprints of protein-protein interactions.

机译:蛋白质相互作用的基于预测的指纹。

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The recognition of protein interaction sites is an important intermediate step toward identification of functionally relevant residues and understanding protein function, facilitating experimental efforts in that regard. Toward that goal, the authors propose a novel representation for the recognition of protein-protein interaction sites that integrates enhanced relative solvent accessibility (RSA) predictions with high resolution structural data. An observation that RSA predictions are biased toward the level of surface exposure consistent with protein complexes led the authors to investigate the difference between the predicted and actual (i.e., observed in an unbound structure) RSA of an amino acid residue as a fingerprint of interaction sites. The authors demonstrate that RSA prediction-based fingerprints of protein interactions significantly improve the discrimination between interacting and noninteracting sites, compared with evolutionary conservation, physicochemical characteristics, structure-derived and other features considered before. On the basis of these observations, the authors developed a new method for the prediction of protein-protein interaction sites, using machine learning approaches to combine the most informative features into the final predictor. For training and validation, the authors used several large sets of protein complexes and derived from them nonredundant representative chains, with interaction sites mapped from multiple complexes. Alternative machine learning techniques are used, including Support Vector Machines and Neural Networks, so as to evaluate the relative effects of the choice of a representation and a specific learning algorithm. The effects of induced fit and uncertainty of the negative (noninteracting) class assignment are also evaluated. Several representative methods from the literature are reimplemented to enable direct comparison of the results. Using rigorous validation protocols, the authors estimated that the new method yields the overall classification accuracy of about 74% and Matthews correlation coefficients of 0.42, as opposed to up to 70% classification accuracy and up to 0.3 Matthews correlation coefficient for methods that do not utilize RSA prediction-based fingerprints. The new method is available at http://sppider.cchmc.org.
机译:蛋白质相互作用位点的识别是迈向鉴定功能相关残基和理解蛋白质功能的重要中间步骤,从而促进了这方面的实验工作。为实现该目标,作者提出了一种识别蛋白质-蛋白质相互作用位点的新方法,该方法将增强的相对溶剂可及性(RSA)预测与高分辨率结构数据相结合。 RSA预测偏向与蛋白质复合物一致的表面暴露水平的观察结果使作者研究了氨基酸残基的RSA预测值与实际值(即在未结合结构中观察到)的RSA之间的差异,作为相互作用位点的指纹。作者证明,与以前考虑的进化保守性,理化特性,结构来源和其他特征相比,基于RSA预测的蛋白质相互作用指纹显着改善了相互作用位点和非相互作用位点之间的区别。基于这些观察,作者开发了一种预测蛋白质-蛋白质相互作用位点的新方法,使用机器学习方法将信息最多的特征组合到最终预测因子中。为了进行训练和验证,作者使用了几套大型的蛋白质复合物,并从中衍生出非冗余的代表性链,并从多种复合物绘制了相互作用位点。使用替代的机器学习技术,包括支持向量机和神经网络,以评估表示形式选择和特定学习算法的相对效果。还评估了归因拟合和否定(非交互)类分配的不确定性的影响。重新实现了文献中的几种代表性方法,可以直接比较结果。使用严格的验证协议,作者估计,新方法的整体分类准确度约为74%,而Matthews相关系数为0.42,而对于未使用方法的分类准确度最高为70%,而Matthews相关系数则为0.3基于RSA预测的指纹。新方法可从http://sppider.cchmc.org获得。

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