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Influence of Protein Abundance on High-Throughput Protein-Protein Interaction Detection

机译:蛋白质丰度对高通量蛋白质-蛋白质相互作用检测的影响

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摘要

Experimental protein-protein interaction (PPI) networks are increasingly being exploited in diverse ways for biological discovery. Accordingly, it is vital to discern their underlying natures by identifying and classifying the various types of deterministic (specific) and probabilistic (nonspecific) interactions detected. To this end, we have analyzed PPI networks determined using a range of high-throughput experimental techniques with the aim of systematically quantifying any biases that arise from the varying cellular abundances of the proteins. We confirm that PPI networks determined using affinity purification methods for yeast and Eschericia coli incorporate a correlation between protein degree, or number of interactions, and cellular abundance. The observed correlations are small but statistically significant and occur in both unprocessed (raw) and processed (high-confidence) data sets. In contrast, the yeast two-hybrid system yields networks that contain no such relationship. While previously commented based on mRNA abundance, our more extensive analysis based on protein abundance confirms a systematic difference between PPI networks determined from the two technologies. We additionally demonstrate that the centrality-lethality rule, which implies that higher-degree proteins are more likely to be essential, may be misleading, as protein abundance measurements identify essential proteins to be more prevalent than nonessential proteins. In fact, we generally find that when there is a degree/abundance correlation, the degree distributions of nonessential and essential proteins are also disparate. Conversely, when there is no degree/abundance correlation, the degree distributions of nonessential and essential proteins are not different. However, we show that essentiality manifests itself as a biological property in all of the yeast PPI networks investigated here via enrichments of interactions between essential proteins. These findings provide valuable insights into the underlying natures of the various high-throughput technologies utilized to detect PPIs and should lead to more effective strategies for the inference and analysis of high-quality PPI data sets.
机译:实验性蛋白质间相互作用(PPI)网络正越来越多地以多种方式用于生物学发现。因此,至关重要的是通过识别和分类所检测到的各种类型的确定性(特定)和概率(非特定)相互作用来识别其基本性质。为此,我们已经分析了使用一系列高通量实验技术确定的PPI网络,目的是系统地量化由于蛋白质的细胞丰度变化而引起的任何偏差。我们确认,使用亲和纯化方法确定的针对酵母和大肠杆菌的PPI网络整合了蛋白质程度或相互作用数与细胞丰度之间的相关性。观察到的相关性很小,但具有统计意义,并且在未处理(原始)和已处理(高置信度)数据集中均会发生。相比之下,酵母双杂交系统产生的网络不包含这种关系。尽管先前基于mRNA丰度进行了评论,但我们基于蛋白质丰度的更广泛分析证实了由两种技术确定的PPI网络之间的系统差异。我们还证明了集中度-致死性规则(这意味着更高程度的蛋白质更可能是必需的)可能会产生误导,因为蛋白质丰度测量确定必需蛋白质比非必需蛋白质更为普遍。实际上,我们通常发现,当存在度/丰度相关性时,非必需和必需蛋白的度分布也完全不同。相反,当不存在度/丰度相关性时,非必需和必需蛋白的度分布没有差异。但是,我们显示出必需性通过丰富必需蛋白之间的相互作用而在所有本文研究的酵母PPI网络中表现为生物学特性。这些发现为用于检测PPI的各种高通量技术的基本性质提供了宝贵的见解,并应为推断和分析高质量PPI数据集提供更有效的策略。

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