• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

HIV-1衣壳核心:直击靶细胞的心脏

HIV-1 Capsid Core: A Bullet to the Heart of the Target Cell.

作者信息

Toccafondi Elenia, Lener Daniela, Negroni Matteo

机构信息

CNRS, Architecture et Réactivité de l'ARN, UPR 9002, Université de Strasbourg, Strasbourg, France.

出版信息

Front Microbiol. 2021 Apr 1;12:652486. doi: 10.3389/fmicb.2021.652486. eCollection 2021.

DOI:10.3389/fmicb.2021.652486
PMID:33868211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8046902/
Abstract

The first step of the intracellular phase of retroviral infection is the release of the viral capsid core in the cytoplasm. This structure contains the viral genetic material that will be reverse transcribed and integrated into the genome of infected cells. Up to recent times, the role of the capsid core was considered essentially to protect this genetic material during the earlier phases of this process. However, increasing evidence demonstrates that the permanence inside the cell of the capsid as an intact, or almost intact, structure is longer than thought. This suggests its involvement in more aspects of the infectious cycle than previously foreseen, particularly in the steps of viral genomic material translocation into the nucleus and in the phases preceding integration. During the trip across the infected cell, many host factors are brought to interact with the capsid, some possessing antiviral properties, others, serving as viral cofactors. All these interactions rely on the properties of the unique component of the capsid core, the capsid protein CA. Likely, the drawback of ensuring these multiple functions is the extreme genetic fragility that has been shown to characterize this protein. Here, we recapitulate the busy agenda of an HIV-1 capsid in the infectious process, in particular in the light of the most recent findings.

摘要

逆转录病毒感染细胞内阶段的第一步是病毒衣壳核心在细胞质中释放。该结构包含病毒遗传物质,这些遗传物质将被逆转录并整合到受感染细胞的基因组中。直到最近,衣壳核心的作用主要被认为是在这一过程的早期阶段保护这种遗传物质。然而,越来越多的证据表明,衣壳作为完整或几乎完整的结构在细胞内的存在时间比之前认为的要长。这表明它在感染周期中涉及的方面比之前预想的更多,特别是在病毒基因组物质转运到细胞核的步骤以及整合之前的阶段。在穿过受感染细胞的过程中,许多宿主因子与衣壳相互作用,一些具有抗病毒特性,另一些则作为病毒辅助因子。所有这些相互作用都依赖于衣壳核心的独特成分——衣壳蛋白CA的特性。可能的是,确保这些多种功能的缺点是已被证明该蛋白具有的极端遗传脆弱性。在此,我们总结了HIV-1衣壳在感染过程中的繁忙日程,特别是根据最新的研究发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/348483adbb81/fmicb-12-652486-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/f28c2dd1611e/fmicb-12-652486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/9521448deae9/fmicb-12-652486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/b5ef1627800d/fmicb-12-652486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/a98dfe4a91cd/fmicb-12-652486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/348483adbb81/fmicb-12-652486-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/f28c2dd1611e/fmicb-12-652486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/9521448deae9/fmicb-12-652486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/b5ef1627800d/fmicb-12-652486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/a98dfe4a91cd/fmicb-12-652486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0b6/8046902/348483adbb81/fmicb-12-652486-g005.jpg

相似文献

1
HIV-1 Capsid Core: A Bullet to the Heart of the Target Cell.HIV-1衣壳核心:直击靶细胞的心脏
Front Microbiol. 2021 Apr 1;12:652486. doi: 10.3389/fmicb.2021.652486. eCollection 2021.
2
HIV-1 uncoating by release of viral cDNA from capsid-like structures in the nucleus of infected cells.HIV-1 脱壳是通过将病毒 cDNA 从感染细胞核内的衣壳样结构中释放出来实现的。
Elife. 2021 Apr 27;10:e64776. doi: 10.7554/eLife.64776.
3
Analysis of CA Content and CPSF6 Dependence of Early HIV-1 Replication Complexes in SupT1-R5 Cells.分析 SupT1-R5 细胞中早期 HIV-1 复制复合物的 CA 含量和 CPSF6 依赖性。
mBio. 2019 Nov 5;10(6):e02501-19. doi: 10.1128/mBio.02501-19.
4
HIV-1 uncoating is facilitated by dynein and kinesin 1.动力蛋白和驱动蛋白1促进了HIV-1衣壳的脱壳。
J Virol. 2014 Dec;88(23):13613-25. doi: 10.1128/JVI.02219-14. Epub 2014 Sep 17.
5
Remodeling of the Core Leads HIV-1 Preintegration Complex into the Nucleus of Human Lymphocytes.核心重构将 HIV-1 整合前复合物导入人淋巴细胞的细胞核。
J Virol. 2020 May 18;94(11). doi: 10.1128/JVI.00135-20.
6
Capsid-Labelled HIV To Investigate the Role of Capsid during Nuclear Import and Integration.衣壳标记的HIV用于研究衣壳在核输入和整合过程中的作用。
J Virol. 2020 Mar 17;94(7). doi: 10.1128/JVI.01024-19.
7
Reverse Transcription Mechanically Initiates HIV-1 Capsid Disassembly.逆转录机械性地启动HIV-1衣壳的解体。
J Virol. 2017 May 26;91(12). doi: 10.1128/JVI.00289-17. Print 2017 Jun 15.
8
Identification of capsid mutations that alter the rate of HIV-1 uncoating in infected cells.鉴定改变感染细胞中 HIV-1 脱壳速度的衣壳突变。
J Virol. 2015 Jan;89(1):643-51. doi: 10.1128/JVI.03043-14. Epub 2014 Oct 22.
9
HIV-1 uncoats in the nucleus near sites of integration.HIV-1 在细胞核内靠近整合位点处脱壳。
Proc Natl Acad Sci U S A. 2020 Mar 10;117(10):5486-5493. doi: 10.1073/pnas.1920631117. Epub 2020 Feb 24.
10
Nuclear pore blockade reveals that HIV-1 completes reverse transcription and uncoating in the nucleus.核孔阻断揭示 HIV-1 在核内完成逆转录和脱壳。
Nat Microbiol. 2020 Sep;5(9):1088-1095. doi: 10.1038/s41564-020-0735-8. Epub 2020 Jun 1.

引用本文的文献

1
Structural insights into HIV-2 CA lattice formation and FG-pocket binding revealed by single-particle cryo-EM.单颗粒冷冻电镜揭示的HIV-2衣壳晶格形成及FG口袋结合的结构见解
Cell Rep. 2025 Feb 25;44(2):115245. doi: 10.1016/j.celrep.2025.115245. Epub 2025 Jan 25.
2
G-quadruplex formation in RNA aptamers selected for binding to HIV-1 capsid.筛选出的用于结合HIV-1衣壳的RNA适配体中的G-四链体形成。
Front Chem. 2024 Oct 22;12:1425515. doi: 10.3389/fchem.2024.1425515. eCollection 2024.
3
Electron tomography visualization of HIV-1 virions trapped by fusion inhibitors to host cells in infected tissues.

本文引用的文献

1
Cone-shaped HIV-1 capsids are transported through intact nuclear pores.锥形 HIV-1 衣壳通过完整的核孔运输。
Cell. 2021 Feb 18;184(4):1032-1046.e18. doi: 10.1016/j.cell.2021.01.025. Epub 2021 Feb 10.
2
Clustering and reverse transcription of HIV-1 genomes in nuclear niches of macrophages.HIV-1 基因组在巨噬细胞核小体中的聚类和逆转录。
EMBO J. 2021 Jan 4;40(1):e105247. doi: 10.15252/embj.2020105247. Epub 2020 Dec 3.
3
HIV-1 Uncoating and Nuclear Import Precede the Completion of Reverse Transcription in Cell Lines and in Primary Macrophages.
电子断层扫描可视化感染组织中融合抑制剂捕获的 HIV-1 病毒颗粒。
J Virol. 2024 Nov 19;98(11):e0143224. doi: 10.1128/jvi.01432-24. Epub 2024 Oct 30.
4
HIV-1 Capsid Uncoating Is a Multistep Process That Proceeds through Defect Formation Followed by Disassembly of the Capsid Lattice.HIV-1 衣壳脱壳是一个多步骤的过程,该过程通过缺陷形成,随后衣壳晶格解体进行。
ACS Nano. 2024 Jan 30;18(4):2928-2947. doi: 10.1021/acsnano.3c07678. Epub 2024 Jan 19.
5
HIV-1 capsid and viral DNA integration.HIV-1 衣壳与病毒 DNA 整合。
mBio. 2024 Jan 16;15(1):e0021222. doi: 10.1128/mbio.00212-22. Epub 2023 Dec 12.
6
The cyclophilin A-binding loop of the capsid regulates the human TRIM5α sensitivity of nonpandemic HIV-1.衣壳蛋白 A 结合环调节非大流行 HIV-1 对人类 TRIM5α 的敏感性。
Proc Natl Acad Sci U S A. 2023 Nov 28;120(48):e2306374120. doi: 10.1073/pnas.2306374120. Epub 2023 Nov 20.
7
Label-free imaging of nuclear membrane for analysis of nuclear import of viral complexes.无标记核膜成像用于分析病毒复合物的核输入
J Virol Methods. 2023 Dec;322:114834. doi: 10.1016/j.jviromet.2023.114834. Epub 2023 Oct 22.
8
Capsid-host interactions for HIV-1 ingress.HIV-1 进入的衣壳-宿主相互作用。
Microbiol Mol Biol Rev. 2023 Dec 20;87(4):e0004822. doi: 10.1128/mmbr.00048-22. Epub 2023 Sep 26.
9
Proline Isomerization: From the Chemistry and Biology to Therapeutic Opportunities.脯氨酸异构化:从化学与生物学至治疗机遇
Biology (Basel). 2023 Jul 14;12(7):1008. doi: 10.3390/biology12071008.
10
The CERV protein of Cer1, a C. elegans LTR retrotransposon, is required for nuclear export of viral genomic RNA and can form giant nuclear rods.Cerv 蛋白是 Cer1,一种线虫 LTR 反转录转座子的蛋白,它是病毒基因组 RNA 核输出所必需的,并且可以形成巨大的核棒。
PLoS Genet. 2023 Jun 29;19(6):e1010804. doi: 10.1371/journal.pgen.1010804. eCollection 2023 Jun.
HIV-1 脱壳和核输入先于逆转录在细胞系和原代巨噬细胞中的完成。
Viruses. 2020 Oct 30;12(11):1234. doi: 10.3390/v12111234.
4
Nuclear Import of the HIV-1 Core Precedes Reverse Transcription and Uncoating.HIV-1 核心的核输入先于逆转录和脱壳。
Cell Rep. 2020 Sep 29;32(13):108201. doi: 10.1016/j.celrep.2020.108201.
5
Atomic-resolution structure of HIV-1 capsid tubes by magic-angle spinning NMR.利用魔角旋转 NMR 技术解析 HIV-1 衣壳管的原子分辨率结构
Nat Struct Mol Biol. 2020 Sep;27(9):863-869. doi: 10.1038/s41594-020-0489-2. Epub 2020 Sep 8.
6
Intrinsic curvature of the HIV-1 CA hexamer underlies capsid topology and interaction with cyclophilin A.HIV-1 CA 六聚体的固有曲率是衣壳拓扑结构和与亲环素 A 相互作用的基础。
Nat Struct Mol Biol. 2020 Sep;27(9):855-862. doi: 10.1038/s41594-020-0467-8. Epub 2020 Aug 3.
7
Nuclear pore blockade reveals that HIV-1 completes reverse transcription and uncoating in the nucleus.核孔阻断揭示 HIV-1 在核内完成逆转录和脱壳。
Nat Microbiol. 2020 Sep;5(9):1088-1095. doi: 10.1038/s41564-020-0735-8. Epub 2020 Jun 1.
8
Remodeling of the Core Leads HIV-1 Preintegration Complex into the Nucleus of Human Lymphocytes.核心重构将 HIV-1 整合前复合物导入人淋巴细胞的细胞核。
J Virol. 2020 May 18;94(11). doi: 10.1128/JVI.00135-20.
9
Cyclophilin A Prevents HIV-1 Restriction in Lymphocytes by Blocking Human TRIM5α Binding to the Viral Core.亲环素 A 通过阻止人源 TRIM5α 与病毒核心结合来防止 HIV-1 在淋巴细胞中的限制。
Cell Rep. 2020 Mar 17;30(11):3766-3777.e6. doi: 10.1016/j.celrep.2020.02.100.
10
TRIM5α self-assembly and compartmentalization of the HIV-1 viral capsid.TRIM5α 自我组装和 HIV-1 病毒衣壳的区室化。
Nat Commun. 2020 Mar 11;11(1):1307. doi: 10.1038/s41467-020-15106-1.