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A Novel Systems-Biology Algorithm for the Analysis of Coordinated Protein Responses Using Quantitative Proteomics

机译:利用定量蛋白质组学分析蛋白质协同反应的新系统生物学算法

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摘要

The coordinated behavior of proteins is central to systems biology. However, the underlying mechanisms are poorly known and methods to analyze coordination by conventional quantitative proteomics are still lacking. We present the Systems Biology Triangle (SBT), a new algorithm that allows the study of protein coordination by pairwise quantitative proteomics. The Systems Biology Triangle detected statistically significant coordination in diverse biological models of very different nature and subjected to different kinds of perturbations. The Systems Biology Triangle also revealed with unprecedented molecular detail an array of coordinated, early protein responses in vascular smooth muscle cells treated at different times with angiotensin-II. These responses included activation of protein synthesis, folding, turnover, and muscle contraction – consistent with a differentiated phenotype—as well as the induction of migration and the repression of cell proliferation and secretion. Remarkably, the majority of the altered functional categories were protein complexes, interaction networks, or metabolic pathways. These changes could not be detected by other algorithms widely used by the proteomics community, and the vast majority of proteins involved have not been described before to be regulated by AngII. The unique capabilities of The Systems Biology Triangle to detect functional protein alterations produced by the coordinated action of proteins in pairwise quantitative proteomics experiments make this algorithm an attractive choice for the biological interpretation of results on a routine basis.
机译:蛋白质的协调行为对系统生物学至关重要。然而,根本的机制知之甚少,仍然缺乏通过常规定量蛋白质组学分析协调的方法。我们提出了系统生物学三角(SBT),这是一种新算法,允许通过成对定量蛋白质组学研究蛋白质配位。系统生物学三角在性质迥异且受不同类型摄动作用的各种生物学模型中检测到统计学上显着的协调。系统生物学三角还以前所未有的分子细节揭示了在不同时间用血管紧张素-II处理的血管平滑肌细胞中一系列协调的早期蛋白质反应。这些反应包括激活蛋白质合成,折叠,周转和肌肉收缩(与分化的表型一致),以及诱导迁移以及抑制细胞增殖和分泌。值得注意的是,大多数改变的功能类别是蛋白质复合物,相互作用网络或代谢途径。蛋白质组学界广泛使用的其他算法无法检测到这些变化,并且之前尚未描述过涉及的绝大多数蛋白质都受AngII调控。系统生物学三角形检测对蛋白质的协同作用在成对定量蛋白质组学实验中产生的功能性蛋白质改变的独特功能,使该算法成为常规对结果进行生物学解释的诱人选择。

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