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

Intracellular Movement of Viruses and Bacteria01:10

Intracellular Movement of Viruses and Bacteria

2.8K
Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a...
2.8K
What are Viruses?00:50

What are Viruses?

114.0K
Overview
114.0K
Protein Complex Assembly02:41

Protein Complex Assembly

10.6K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types.  Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
10.6K
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

45.7K
Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the...
45.7K
Intralumenal Vesicles and Multivesicular Bodies01:38

Intralumenal Vesicles and Multivesicular Bodies

3.4K
Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
3.4K
Viruses with RNA Genomes01:29

Viruses with RNA Genomes

3
RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
3

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

Hepatitis B Virus e Antigen in Mother-to-Child Transmission and Clinical Management of Hepatitis B.

Viruses·2025
Same author

Effects of cellular membranes and the precore protein on hepatitis B virus core particle assembly and DNA replication.

mBio·2025
Same author

Hepatitis B virus e antigen induces atypical metabolism and differentially regulates programmed cell deaths of macrophages.

PLoS pathogens·2024
Same author

Regulation of Mitochondrial Metabolism by Hepatitis B Virus.

Viruses·2023
Same author

Virology under the Microscope-a Call for Rational Discourse.

Journal of virology·2023
Same author

Virology under the Microscope-a Call for Rational Discourse.

mBio·2023

相关实验视频

Updated: Jun 9, 2025

A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
11:34

A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target

Published on: May 10, 2022

2.2K

乙型肝炎病毒的进入,聚集和退出.

Yu-Chen Chuang1, J-H James Ou1

  • 1Department of Molecular Microbiology and Immunology, University of Southern California Keck School of Medicine, Los Angeles, California, USA.

Microbiology and molecular biology reviews : MMBR
|October 23, 2024
PubMed
概括

乙型肝炎病毒 (HBV) 在全球感染了数百万人,导致严重的肝病. 这篇评论详细介绍了HBV的细节.

科学领域:

  • 病毒学 病毒学
  • 肝病学 肝病学是一种肝病学.
  • 分子生物学分子生物学

背景情况:

  • 乙型肝炎病毒 (HBV) 是一个主要的全球健康问题,每年感染2.5亿人,造成100多万人死亡.
  • 乙型肝炎病毒感染导致严重的肝脏疾病,如肝硬化和肝细胞癌.
  • 了解HBV的生命周期对于开发有效的治疗方法至关重要.

研究的目的:

  • 审查和讨论乙型肝炎病毒进入,聚集和退出的分子途径.
  • 为了将这些过程与其他包裹性肝炎病毒 (如型肝炎病毒和型肝炎病毒) 的过程进行比较.
  • 为改善患者治疗提供有关HBV复制和病原学的见解.

主要方法:

  • 关于HBV分子通路的最新研究的文献综述.
  • 用型肝炎病毒和型肝炎病毒对HBV过程的比较分析.
  • 讨论病毒的进入,囊组合和退出机制.

主要成果:

  • 在了解HBV与肝细胞,核运输和病毒颗粒释放的相互作用方面取得了重大进展.
  • 关键的分子步骤包括膜蛋白-受体相互作用进入,核囊向核递送,以及随后的病毒RNA转录.
  • 病毒囊组合发生在细胞核或细胞质中,可能涉及细胞膜,病毒退出之前.
关键词:
两体是一种两体.自自是自的过程.克拉林介导的内细胞分裂异位细胞形成的表细胞化.乙型肝炎病毒的感染.在C型肝炎病毒的感染中,甲型肝炎的三角病毒.多个体的多个体体的身体.病毒入口病毒入口.

更多相关视频

Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
09:35

Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle

Published on: February 1, 2017

13.2K
Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
09:02

Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells

Published on: June 5, 2020

7.3K

相关实验视频

Last Updated: Jun 9, 2025

A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
11:34

A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target

Published on: May 10, 2022

2.2K
Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle
09:35

Development of a Hepatitis B Virus Reporter System to Monitor the Early Stages of the Replication Cycle

Published on: February 1, 2017

13.2K
Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
09:02

Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells

Published on: June 5, 2020

7.3K

结论:

  • 了解HBV进入,聚集和退出的详细分子机制对于理解病毒复制和疾病进展至关重要.
  • 这种知识对于开发新型治疗策略来对抗HBV感染及其相关肝脏疾病至关重要.
  • 与其他肝炎病毒的比较见解突出了它们的复制周期的保存和独特方面.