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可视化和分析与血细胞靶向自身免疫性疾病相关的蛋白质相互作用网络。

Visualization and analysis of the interaction network of proteins associated with blood-cell targeting autoimmune diseases.

机构信息

Department of Biology, School of Sciences, National and Kapodistrian University of Athens, Panepistimiopolis, Athens 157 01, Greece.

Department of Biology, School of Sciences, National and Kapodistrian University of Athens, Panepistimiopolis, Athens 157 01, Greece.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2020 May 1;1866(5):165714. doi: 10.1016/j.bbadis.2020.165714. Epub 2020 Feb 3.

Abstract

Blood-cell targeting Autoimmune Diseases (BLADs) are complex diseases that affect blood cell formation or prevent blood cell production. Since these clinical conditions are gathering growing attention, experimental approaches are being used to investigate the mechanisms behind their pathogenesis and to identify proteins associated with them. However, computational approaches have not been utilized extensively in the study of BLADs. This study aims to investigate the interaction network of proteins associated with BLADs (BLAD interactome) and to identify novel associations with other human proteins. The method followed in this study combines information regarding protein-protein interaction network properties and autoimmune disease terms. Proteins with high network scores and statistically significant autoimmune disease term enrichment were obtained and 14 of them were designated as candidate proteins associated with BLADs. Additionally, clustering analysis of the BLAD interactome was used and allowed the detection of 17 proteins that act as "connectors" of different BLADs. We expect our findings to further extend experimental efforts for the investigation of the pathogenesis and the relationships of BLADs.

摘要

针对血细胞的自身免疫疾病 (BLADs) 是影响血细胞形成或阻止血细胞生成的复杂疾病。由于这些临床情况受到越来越多的关注,因此正在采用实验方法来研究其发病机制背后的机制,并确定与之相关的蛋白质。然而,计算方法在 BLADs 的研究中并未得到广泛应用。本研究旨在研究与 BLADs 相关的蛋白质相互作用网络 (BLAD 相互作用组),并确定与其他人类蛋白质的新关联。本研究中采用的方法结合了有关蛋白质-蛋白质相互作用网络特性和自身免疫性疾病术语的信息。获得了具有高网络评分和统计学上显著的自身免疫性疾病术语富集的蛋白质,其中 14 种被指定为与 BLADs 相关的候选蛋白质。此外,还对 BLAD 相互作用组进行了聚类分析,检测到 17 种作为不同 BLADs“连接器”的蛋白质。我们期望我们的发现能够进一步扩展实验研究,以研究 BLADs 的发病机制和相互关系。

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