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

Lytic Cycle of Bacteriophages01:30

Lytic Cycle of Bacteriophages

70.1K
Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the...
70.1K
Lysosomal Hydrolases01:22

Lysosomal Hydrolases

3.7K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.7K
Lysogenic Cycle of Bacteriophages00:43

Lysogenic Cycle of Bacteriophages

61.7K
In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
61.7K

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

Molecular mechanism of cholesterol-dependent membrane fusion in SARS-CoV-2 entry.

Signal transduction and targeted therapy·2026
Same author

Structural basis of mpox virus A30/H2 subcomplex formation.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Intranasal vaccine combining adenovirus and trimeric subunit protein provides superior immunity against SARS-CoV-2 Omicron variant.

Nature biomedical engineering·2025
Same author

Structural basis and mode of action for two broadly neutralizing nanobodies targeting the highly conserved spike stem-helix of sarbecoviruses including SARS-CoV-2 and its variants.

PLoS pathogens·2025
Same author

A recombinant protein vaccine induces protective immunity against SARS-CoV-2 JN.1 and XBB-lineage subvariants.

Signal transduction and targeted therapy·2025
Same author

Recombinant XBB.1.5 boosters induce robust neutralization against KP.2- and KP.3-included JN.1 sublineages.

Signal transduction and targeted therapy·2025

相关实验视频

Updated: May 27, 2025

Sedimentation Equilibrium of a Small Oligomer-forming Membrane Protein: Effect of Histidine Protonation on Pentameric Stability
09:49

Sedimentation Equilibrium of a Small Oligomer-forming Membrane Protein: Effect of Histidine Protonation on Pentameric Stability

Published on: April 2, 2015

10.5K

两种被困在融合前和融合后状态中的lyssavirus糖蛋白的结构以及与pH值降低一起对空间-时间形态转换的含义.

Fanli Yang1, Sheng Lin1, Xin Yuan1

  • 1Department of Emergency Medicine, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

PLoS pathogens
|February 19, 2025
PubMed
概括

研究人员绘制了Ikoma和Mokola lyssavirus糖蛋白的结构图,揭示了一种序列形状变化模型. 这一发现有助于开发针对lyssaviruses的新疫苗和抗病毒药物.

更多相关视频

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting
08:40

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting

Published on: March 1, 2019

58.9K
High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water
08:48

High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water

Published on: April 28, 2022

1.7K

相关实验视频

Last Updated: May 27, 2025

Sedimentation Equilibrium of a Small Oligomer-forming Membrane Protein: Effect of Histidine Protonation on Pentameric Stability
09:49

Sedimentation Equilibrium of a Small Oligomer-forming Membrane Protein: Effect of Histidine Protonation on Pentameric Stability

Published on: April 2, 2015

10.5K
Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting
08:40

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting

Published on: March 1, 2019

58.9K
High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water
08:48

High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water

Published on: April 28, 2022

1.7K

科学领域:

  • 病毒学 病毒学
  • 结构生物学 结构生物学
  • 免疫学 免疫学 免疫学

背景情况:

  • Lyssavirus 糖蛋白对于病毒进入至关重要,也是中和抗体的关键目标.
  • 这种糖蛋白在膜融合过程中经历了显著的低pH诱导的构造变化.

研究的目的:

  • 为了确定Ikoma lyssavirus和Mokola lyssavirus糖蛋白的结构.
  • 为了阐明在膜融合过程中lyssavirus糖蛋白的构造过渡.
  • 为lyssaviral glycoproteins开发一个顺序的构造-过渡模型.

主要方法:

  • 进行X射线晶体学以确定糖蛋白结构.
  • 对可用的lyssaviral糖蛋白结构的分析.
  • 表面等离子体共振试验用于研究pH调节的相互作用.

主要成果:

  • 确定了Ikoma和Mokola lyssavirus糖蛋白的结构,代表了融合前和融合后的状态.
  • 提出了一种连续的形状转变模型,涉及从发针到线性形状的二次结构变化.
  • 特定域之间的pH调节的相互作用促进了形状变化.

结论:

  • 阐明的结构特征提供了关于lyssavirus糖蛋白功能的见解.
  • 了解这些构造动态可以指导新型疫苗和抗病毒疗法对抗lyssaviruses的设计.