先天免疫系统
泛素
泛素连接酶
干扰素
生物
干扰素调节因子
信号转导
细胞生物学
基因
干扰素基因刺激剂
计算生物学
遗传学
受体
作者
Ting Li,Chunfu Zheng,Huifang Zhu
出处
期刊:Methods in molecular biology
日期:2024-08-27
卷期号:: 1-7
标识
DOI:10.1007/978-1-0716-4108-8_1
摘要
Antiviral innate immunity is a complicated system initiated by the induction of type I interferon (IFN-I) and downstream interferon-stimulated genes (ISGs) and is finely regulated by numerous positive and negative factors at different signaling adaptors. During this process, posttranslational modifications, especially ubiquitination, are the most common regulatory strategy used by the host to switch the antiviral innate signaling pathway and are mainly controlled by E3 ubiquitin ligases from different protein families. A comprehensive understanding of the regulatory mechanisms and a novel discovery of regulatory factors involved in the IFN-I signaling pathway are important for researchers to identify novel therapeutic targets against viral infectious diseases based on innate immunotherapy. In this section, we use the E3 ubiquitin ligase as an example to guide the identification of a protein belonging to the RING Finger (RNF) family that regulates the RIG-I-mediated IFN-I pathway through ubiquitination.
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