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干扰素刺激基因的蛋白质相互作用网络扩展了先天免疫系统景观。

A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape.

机构信息

Innate Immunity Laboratory, Max-Planck Institute of Biochemistry, Munich, Germany.

Institute of Virology, School of Medicine, Technical University of Munich, Munich, Germany.

出版信息

Nat Immunol. 2019 Apr;20(4):493-502. doi: 10.1038/s41590-019-0323-3. Epub 2019 Mar 4.

Abstract

Interferon-stimulated genes (ISGs) form the backbone of the innate immune system and are important for limiting intra- and intercellular viral replication and spread. We conducted a mass-spectrometry-based survey to understand the fundamental organization of the innate immune system and to explore the molecular functions of individual ISGs. We identified interactions between 104 ISGs and 1,401 cellular binding partners engaging in 2,734 high-confidence interactions. 90% of these interactions are unreported so far, and our survey therefore illuminates a far wider activity spectrum of ISGs than is currently known. Integration of the resulting ISG-interaction network with published datasets and functional studies allowed us to identify regulators of immunity and processes related to the immune system. Given the extraordinary robustness of the innate immune system, this ISG network may serve as a blueprint for therapeutic targeting of cellular systems to efficiently fight viral infections.

摘要

干扰素刺激基因(ISGs)构成了先天免疫系统的骨干,对于限制细胞内和细胞间病毒复制和传播非常重要。我们进行了一项基于质谱的调查,以了解先天免疫系统的基本组织,并探索单个 ISGs 的分子功能。我们鉴定了 104 个 ISGs 与 1401 个细胞结合伴侣之间的相互作用,这些相互作用涉及 2734 个高置信度的相互作用。到目前为止,这些相互作用中有 90%是未被报道的,因此我们的调查揭示了 ISGs 的活性谱远比目前已知的要广泛得多。将由此产生的 ISG 相互作用网络与已发表的数据集和功能研究整合在一起,使我们能够识别免疫调节因子和与免疫系统相关的过程。鉴于先天免疫系统的非凡稳健性,这个 ISG 网络可以作为针对细胞系统进行治疗性靶向的蓝图,以有效对抗病毒感染。

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