Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Viral Mutations00:36

Viral Mutations

32.3K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.3K
Viral Recombination00:57

Viral Recombination

23.4K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Rasputin/G3BP mediates subversion of antiviral immunity by o'nyong-nyong virus in Anopheles coluzzii.

PLoS pathogens·2026
Same author

Arf1 is involved in Neisseria meningitidis-induced cortical branched F-actin network reorganization.

EMBO reports·2026
Same author

Pneumococcus uses COMMD2 to alter host cellular immunity.

Nature communications·2026
Same author

Lassa and Mopeia viruses produce different RIG-I-activating RNA in the absence of a functional viral exoribonuclease domain.

Journal of virology·2026
Same author

Direct carbapenemase typing from disc diffusion antibiograms with MALCA (MAchine Learning CArbapenemase).

Nature communications·2026
Same author

<i>Staphylococcus epidermidis</i> DnaK alters biofilm formation and proteome in <i>Staphylococcus aureus</i> CIP 107093.

Frontiers in microbiology·2026

相关实验视频

Updated: Jun 26, 2025

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
11:28

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus

Published on: October 7, 2011

11.0K

应用逆遗传学研究麻疹病毒与宿主之间的相互作用.

Heidy Vera-Peralta1,2, Valerie Najburg1, Chantal Combredet1

  • 1Institut Pasteur, Université Paris Cité, Innovation Lab: Vaccines, Paris, France.

Methods in molecular biology (Clifton, N.J.)
|May 14, 2024
PubMed
概括

这项研究引入了一种使用重组病毒的新方法,用于在实际感染期间识别病毒与宿主蛋白相互作用. 这种方法克服了以前技术的局限性,为病毒复制提供了更准确的见解.

关键词:
关联性净化净化方法麻疹病毒病毒.复合病毒的复合病毒.反向遗传学是一种逆向遗传学.标签: 蛋白质 标签: 蛋白质病毒与宿主之间的相互作用

更多相关视频

Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production
08:32

Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production

Published on: March 2, 2014

10.5K
Reverse Genetics Mediated Recovery of Infectious Murine Norovirus
13:48

Reverse Genetics Mediated Recovery of Infectious Murine Norovirus

Published on: June 24, 2012

16.6K

相关实验视频

Last Updated: Jun 26, 2025

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
11:28

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus

Published on: October 7, 2011

11.0K
Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production
08:32

Dissecting Innate Immune Signaling in Viral Evasion of Cytokine Production

Published on: March 2, 2014

10.5K
Reverse Genetics Mediated Recovery of Infectious Murine Norovirus
13:48

Reverse Genetics Mediated Recovery of Infectious Murine Norovirus

Published on: June 24, 2012

16.6K

科学领域:

  • 病毒学 病毒学
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 了解病毒与宿主之间的相互作用对于破译病毒复制至关重要.
  • 目前的方法,如酵母双混合和亲和净化质谱 (AP-MS) 有局限性,检测真实感染环境之外的相互作用,并可能产生人工结果.

研究的目的:

  • 开发和提出一种新的策略,用于在真实的病毒感染环境中识别病毒-宿主蛋白-蛋白相互作用.
  • 通过捕捉感染期间发生的相互作用来克服现有方法的局限性.

主要方法:

  • 开发用于表达标记病毒蛋白的重组病毒.
  • 在感染宿主细胞上直接应用亲和性净化质谱法 (AP-MS),以捕获病毒宿主蛋白质复合体在其原生环境中 ("病毒环境中的AP-MS").

主要成果:

  • 描述的策略可以捕获直接和间接的蛋白质合作伙伴,参与病毒与宿主相互作用.
  • 直接从受感染细胞中净化相互作用的共同复合物,可以进行更准确的表征.

结论:

  • 这种新型的AP-MS在病毒背景方法中的方法为研究病毒-宿主蛋白质-蛋白质相互作用提供了更具生物学相关性的方法.
  • 该技术提高了识别互动的准确性,这对于理解病毒复制至关重要.