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Large-Scale Protein-Protein Interactions Detection by Integrating Big Biosensing Data with Computational Model

机译:通过将大的生物传感数据与计算模型集成来进行大规模蛋白质-蛋白质相互作用的检测

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Protein-protein interactions are the basis of biological functions, and studying these interactions on a molecular level is of crucial importance for understanding the functionality of a living cell. During the past decade, biosensors have emerged as an important tool for the high-throughput identification of proteins and their interactions. However, the high-throughput experimental methods for identifying PPIs are both time-consuming and expensive. On the other hand, high-throughput PPI data are often associated with high false-positive and high false-negative rates. Targeting at these problems, we propose a method for PPI detection by integrating biosensor-based PPI data with a novel computational model. This method was developed based on the algorithm of extreme learning machine combined with a novel representation of protein sequence descriptor. When performed on the large-scale human protein interaction dataset, the proposed method achieved 84.8% prediction accuracy with 84.08% sensitivity at the specificity of 85.53%. We conducted more extensive experiments to compare the proposed method with the state-of-the-art techniques, support vector machine. The achieved results demonstrate that our approach is very promising for detecting new PPIs, and it can be a helpful supplement for biosensor-based PPI data detection.
机译:蛋白质-蛋白质相互作用是生物学功能的基础,在分子水平上研究这些相互作用对于理解活细胞的功能至关重要。在过去的十年中,生物传感器已成为用于高通量鉴定蛋白质及其相互作用的重要工具。但是,用于识别PPI的高通量实验方法既耗时又昂贵。另一方面,高通量PPI数据通常与高假阳性和高假阴性率相关。针对这些问题,我们提出了一种通过将基于生物传感器的PPI数据与新型计算模型相集成的PPI检测方法。该方法是在极限学习机算法的基础上,结合蛋白质序列描述符的一种新颖表示法开发的。当在大规模人蛋白质相互作用数据集上进行时,所提出的方法在85.53%的特异性下达到了84.8%的预测准确度和84.08%的灵敏度。我们进行了更广泛的实验,以将所提出的方法与最新技术,支持向量机进行比较。取得的成果表明,我们的方法在检测新的PPI方面非常有前途,并且可以作为基于生物传感器的PPI数据检测的有用补充。

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