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综合方法揭示 RNA 病毒重编程细胞环境的机制。

Integrated approaches to reveal mechanisms by which RNA viruses reprogram the cellular environment.

机构信息

Department of Chemistry, Case Western Reserve University, Cleveland, OH 44106, United States.

Department of Chemistry, Case Western Reserve University, Cleveland, OH 44106, United States.

出版信息

Methods. 2020 Nov 1;183:50-56. doi: 10.1016/j.ymeth.2020.06.013. Epub 2020 Jul 2.

DOI:10.1016/j.ymeth.2020.06.013
PMID:32622045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7329689/
Abstract

RNA viruses are major threats to global society and mass outbreaks can cause long-lasting damage to international economies. RNA and related retro viruses represent a large and diverse family that contribute to the onset of human diseases such as AIDS; certain cancers like T cell lymphoma; severe acute respiratory illnesses as seen with COVID-19; and others. The hallmark of this viral family is the storage of genetic material in the form of RNA, and upon infecting host cells, their RNA genomes reprogram the cellular environment to favor productive viral replication. RNA is a multifunctional biomolecule that not only stores and transmits heritable information, but it also has the capacity to catalyze complex biochemical reactions. It is therefore no surprise that RNA viruses use this functional diversity to their advantage to sustain chronic or lifelong infections. Efforts to subvert RNA viruses therefore requires a deep understanding of the mechanisms by which these pathogens usurp cellular machinery. Here, we briefly summarize several experimental techniques that individually inform on key physicochemical features of viral RNA genomes and their interactions with proteins. Each of these techniques provide important vantage points to understand the complexities of virus-host interactions, but we attempt to make the case that by integrating these and similar methods, more vivid descriptions of how viruses reprogram the cellular environment emerges. These vivid descriptions should expedite the identification of novel therapeutic targets.

摘要

RNA 病毒是对全球社会的主要威胁,大规模爆发会对国际经济造成持久的损害。RNA 病毒和相关的逆转录病毒是一个庞大而多样的家族,它们会导致人类疾病的发生,如艾滋病;某些癌症,如 T 细胞淋巴瘤;像 COVID-19 这样的严重急性呼吸系统疾病;以及其他疾病。这个病毒家族的标志是将遗传物质以 RNA 的形式储存,在感染宿主细胞后,它们的 RNA 基因组重新编程细胞环境,有利于病毒的复制。RNA 是一种多功能的生物分子,不仅可以储存和传递遗传信息,还具有催化复杂生化反应的能力。因此,RNA 病毒利用这种功能多样性来维持慢性或终身感染也就不足为奇了。因此,颠覆 RNA 病毒的努力需要深入了解这些病原体如何篡夺细胞机制的机制。在这里,我们简要总结了几种实验技术,这些技术分别提供了有关病毒 RNA 基因组及其与蛋白质相互作用的关键物理化学特征的信息。这些技术中的每一种都为理解病毒-宿主相互作用的复杂性提供了重要的视角,但我们试图说明的是,通过整合这些技术和类似的方法,可以更生动地描述病毒如何重新编程细胞环境。这些生动的描述应该会加速确定新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d58/7329689/b0712831de7c/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d58/7329689/545c921d10f3/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d58/7329689/b0712831de7c/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d58/7329689/545c921d10f3/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d58/7329689/b0712831de7c/gr2_lrg.jpg

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本文引用的文献

1
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Proc Natl Acad Sci U S A. 2020 May 26;117(21):11727-11734. doi: 10.1073/pnas.2003138117. Epub 2020 May 6.
2
Structural elucidation of SARS-CoV-2 vital proteins: Computational methods reveal potential drug candidates against main protease, Nsp12 polymerase and Nsp13 helicase.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)关键蛋白的结构解析:计算方法揭示了针对主要蛋白酶、Nsp12聚合酶和Nsp13解旋酶的潜在候选药物。
J Pharm Anal. 2020 Aug;10(4):320-328. doi: 10.1016/j.jpha.2020.04.008. Epub 2020 Apr 28.
3
Identification of potential binders of the main protease 3CL of the COVID-19 via structure-based ligand design and molecular modeling.
关于膜联蛋白 A2 在 COVID-19 发病机制和感染后并发症中可能作用的分子见解。
Int J Mol Sci. 2021 Oct 13;22(20):11028. doi: 10.3390/ijms222011028.
4
Editorial for "Methods to characterize virus small RNAs and RNA structures".《“病毒小RNA及RNA结构的表征方法”》社论
Methods. 2020 Nov 1;183:1-3. doi: 10.1016/j.ymeth.2020.10.007. Epub 2020 Oct 16.
5
Roadblocks and fast tracks: How RNA binding proteins affect the viral RNA journey in the cell.道路与捷径:RNA 结合蛋白如何影响细胞内的病毒 RNA 旅程。
Semin Cell Dev Biol. 2021 Mar;111:86-100. doi: 10.1016/j.semcdb.2020.08.006. Epub 2020 Aug 23.
通过基于结构的配体设计和分子建模鉴定新型冠状病毒主要蛋白酶3CL的潜在结合剂
Chem Phys Lett. 2020 Jul;750:137489. doi: 10.1016/j.cplett.2020.137489. Epub 2020 Apr 18.
4
Viral RNA structure analysis using DMS-MaPseq.利用 DMS-MaPseq 分析病毒 RNA 结构。
Methods. 2020 Nov 1;183:68-75. doi: 10.1016/j.ymeth.2020.04.001. Epub 2020 Apr 3.
5
Research and Development on Therapeutic Agents and Vaccines for COVID-19 and Related Human Coronavirus Diseases.新型冠状病毒肺炎及相关人类冠状病毒疾病治疗药物和疫苗的研发
ACS Cent Sci. 2020 Mar 25;6(3):315-331. doi: 10.1021/acscentsci.0c00272. Epub 2020 Mar 12.
6
The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreak - an update on the status.2019 冠状病毒病(COVID-19)疫情的起源、传播和临床治疗——现状更新。
Mil Med Res. 2020 Mar 13;7(1):11. doi: 10.1186/s40779-020-00240-0.
7
COVID-19 and the cardiovascular system.新型冠状病毒肺炎与心血管系统。
Nat Rev Cardiol. 2020 May;17(5):259-260. doi: 10.1038/s41569-020-0360-5.
8
The species Severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2.严重急性呼吸综合征相关冠状病毒:将 2019-nCoV 进行分类并命名为 SARS-CoV-2。
Nat Microbiol. 2020 Apr;5(4):536-544. doi: 10.1038/s41564-020-0695-z. Epub 2020 Mar 2.
9
The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak.冠状病毒病(COVID-19)疫情的流行病学和发病机制。
J Autoimmun. 2020 May;109:102433. doi: 10.1016/j.jaut.2020.102433. Epub 2020 Feb 26.
10
A pneumonia outbreak associated with a new coronavirus of probable bat origin.一种新型冠状病毒引发的肺炎疫情,该病毒可能来源于蝙蝠。
Nature. 2020 Mar;579(7798):270-273. doi: 10.1038/s41586-020-2012-7. Epub 2020 Feb 3.