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RIG-I 样受体:RIG-I 和 MDA5 的比较结构与功能分析。

Comparative Structure and Function Analysis of the RIG-I-Like Receptors: RIG-I and MDA5.

机构信息

Biochemistry, Molecular Biology, and Biophysics Graduate Program, University of Minnesota, Twin Cities, St. Paul, MN, United States.

Department of Veterinary & Biomedical Sciences, University of Minnesota, Twin Cities, St. Paul, MN, United States.

出版信息

Front Immunol. 2019 Jul 17;10:1586. doi: 10.3389/fimmu.2019.01586. eCollection 2019.

Abstract

RIG-I (Retinoic acid-inducible gene I) and MDA5 (Melanoma Differentiation-Associated protein 5), collectively known as the RIG-I-like receptors (RLRs), are key protein sensors of the pathogen-associated molecular patterns (PAMPs) in the form of viral double-stranded RNA (dsRNA) motifs to induce expression of type 1 interferons (IFN1) (IFNα and IFNβ) and other pro-inflammatory cytokines during the early stage of viral infection. While RIG-I and MDA5 share many genetic, structural and functional similarities, there is increasing evidence that they can have significantly different strategies to recognize different pathogens, PAMPs, and in different host species. This review article discusses the similarities and differences between RIG-I and MDA5 from multiple perspectives, including their structures, evolution and functional relationships with other cellular proteins, their differential mechanisms of distinguishing between host and viral dsRNAs and interactions with host and viral protein factors, and their immunogenic signaling. A comprehensive comparative analysis can help inform future studies of RIG-I and MDA5 in order to fully understand their functions in order to optimize potential therapeutic approaches targeting them.

摘要

RIG-I(维甲酸诱导基因 I)和 MDA5(黑色素瘤分化相关蛋白 5),统称为 RIG-I 样受体(RLRs),是病毒双链 RNA(dsRNA)基序形式的病原体相关分子模式(PAMPs)的关键蛋白传感器,可在病毒感染的早期诱导 1 型干扰素(IFN1)(IFNα 和 IFNβ)和其他促炎细胞因子的表达。虽然 RIG-I 和 MDA5 具有许多遗传、结构和功能上的相似性,但越来越多的证据表明,它们可以采用非常不同的策略来识别不同的病原体、PAMPs ,以及在不同的宿主物种中。这篇综述文章从多个角度讨论了 RIG-I 和 MDA5 的相似性和差异性,包括它们的结构、进化以及与其他细胞蛋白的功能关系,它们区分宿主和病毒 dsRNA 的不同机制,以及与宿主和病毒蛋白因子的相互作用和免疫原性信号。全面的比较分析可以帮助为未来的 RIG-I 和 MDA5 研究提供信息,以充分了解它们的功能,从而优化针对它们的潜在治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/461a/6652118/ff73f3989b90/fimmu-10-01586-g0001.jpg

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