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PAMPer 和 tRIGer:配体诱导的 RIG-I 激活。

PAMPer and tRIGer: ligand-induced activation of RIG-I.

机构信息

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta GA, 30333, United States.

出版信息

Trends Biochem Sci. 2011 Jun;36(6):314-9. doi: 10.1016/j.tibs.2011.03.003. Epub 2011 Apr 14.

Abstract

Retinoic-acid-inducible gene-I (RIG-I) is an important component of the innate immune response to many RNA viruses that limits viral replication until adaptive immunity becomes available to clear the infection. Upon binding to the nucleic acid genomes and replication intermediates of these viruses, RIG-I undergoes a complex activation process that involves post-translational modifications and structural rearrangements. Once activated, RIG-I upregulates well-studied signal transduction pathways that lead to the production of type-I interferons (IFNs) and a large variety of antiviral IFN-stimulated genes. Thus, an effective antiviral response is dependent on the interaction between pathogen-derived ligands and RIG-I. Recent work has begun to clarify the required characteristics of RIG-I activators and is setting the stage for the identification of authentic ligands used during viral infection.

摘要

视黄酸诱导基因 I(RIG-I)是对许多 RNA 病毒固有免疫反应的重要组成部分,它限制了病毒的复制,直到适应性免疫能够清除感染。RIG-I 在与这些病毒的核酸基因组和复制中间体结合后,会经历一个涉及翻译后修饰和结构重排的复杂激活过程。一旦被激活,RIG-I 就会上调研究得很好的信号转导途径,导致产生 I 型干扰素(IFN)和多种抗病毒 IFN 刺激基因。因此,有效的抗病毒反应取决于病原体衍生配体与 RIG-I 之间的相互作用。最近的工作已经开始阐明 RIG-I 激活剂的必需特征,并为鉴定病毒感染过程中使用的真实配体奠定了基础。

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