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A Bayesian approach for estimating protein–protein interactions by integrating structural and non-structural biological data

机译:通过整合结构和非结构生物学数据估算蛋白质相互作用的贝叶斯方法

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摘要

Accurate elucidation of genome wide protein–protein interactions is crucial for understanding thernregulatory processes of the cell. High-throughput techniques, such as the yeast-2-hybrid (Y2H) assay,rnco-immunoprecipitation (co-IP), mass spectrometric (MS) protein complex identification, affinityrnpurification (AP) etc., are generally relied upon to determine protein interactions. Unfortunately, eachrntype of method is inherently subject to different types of noise and results in false positive interactions.rnOn the other hand, precise understanding of proteins, especially knowledge of their functionalrnassociations is necessary for understanding how complex molecular machines function. To solve thisrnproblem, computational techniques are generally relied upon to precisely predict protein interactions.rnIn this work, we present a novel method that combines structural and non-structural biological data tornprecisely predict protein interactions. The conceptual novelty of our approach lies in identifying andrnprecisely associating biological information that provides substantial interaction clues. Our modelrncombines structural and non-structural information using Bayesian statistics to calculate the likelihoodrnof each interaction. The proposed model is tested on Saccharomyces cerevisiae’s interactions extractedrnfrom the DIP and IntAct databases and provides substantial improvements in terms of accuracy, precision,rnrecall and F1 score, as compared with the most widely used related state-of-the-art techniques.
机译:准确阐明全基因组蛋白之间的相互作用对于理解细胞的调控过程至关重要。通常使用高通量技术来确定蛋白质,例如酵母2-杂交(Y2H)检测,rnco免疫沉淀(co-IP),质谱(MS)蛋白质复合物鉴定,亲和纯化(AP)等。互动。不幸的是,每种类型的方法都固有地受到不同类型的噪声的影响,并导致假阳性相互作用。另一方面,对蛋白质的精确理解,尤其是其功能关联的知识,对于理解复杂的分子机器如何发挥作用是必需的。为了解决这个问题,通常依赖于计算技术来精确预测蛋白质相互作用。在这项工作中,我们提出了一种结合结构和非结构生物学数据来精确预测蛋白质相互作用的新方法。我们方法的概念新颖之处在于识别并精确地关联提供大量交互线索的生物学信息。我们的模型使用贝叶斯统计信息来组合结构信息和非结构信息,以计算每次相互作用的可能性。与从最广泛使用的相关最新技术相比,该提议的模型已通过从DIP和IntAct数据库中提取的酿酒酵母的相互作用进行了测试,并在准确性,准确性,召回率和F1得分方面提供了实质性的改进。

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  • 来源
    《Molecular BioSystems》 |2017年第12期|2592-2602|共11页
  • 作者单位

    Department of Computer Science, FAST National University of Computer &Emerging Sciences, Peshawar, Pakistan;

    Department of Electrical Engineering, FAST National University of Computer &Emerging Sciences, Peshawar, Pakistan;

    Department of Electrical Engineering, FAST National University of Computer &Emerging Sciences, Peshawar, Pakistan;

    Department of Computer Science, FAST National University of Computer &Emerging Sciences, Lahore, Pakistan;

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