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

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 for adaptive...
Cross-reactivity00:42

Cross-reactivity

Overview
Antigens Involved in Adaptive Immunity01:26

Antigens Involved in Adaptive Immunity

An antigen is any substance the immune system identifies as foreign and potentially harmful to the body, prompting an immune response. Antigens have two functional properties: immunogenicity and reactivity. Immunogenicity is the ability of an antigen to stimulate a specific immune response. At the same time, reactivity describes the antigen's ability to react with the cells and antibodies produced in response to it.
Complete Antigens
Complete antigens possess both immunogenicity and reactivity.
Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...

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

Vaccine-Associated Maintenance of Epithelial Integrity Correlated With Protection Against Virus Entry.

The Journal of infectious diseases·2018
Same author

Vaccine-modified NF-kB and GR signaling in cervicovaginal epithelium correlates with protection.

Mucosal immunology·2017
Same author

Probing lepton flavour violation via neutrinoless [Formula: see text] decays with the ATLAS detector.

The European physical journal. C, Particles and fields·2017
Same author

A new method to distinguish hadronically decaying boosted <i>Z</i> bosons from <i>W</i> bosons using the ATLAS detector.

The European physical journal. C, Particles and fields·2017
Same author

Measurement of the centrality dependence of the charged-particle pseudorapidity distribution in proton-lead collisions at [Formula: see text] TeV with the ATLAS detector.

The European physical journal. C, Particles and fields·2017
Same author

Search for new phenomena in events with at least three photons collected in <i>pp</i> collisions at [Formula: see text] = 8 TeV with the ATLAS detector.

The European physical journal. C, Particles and fields·2017

相关实验视频

Updated: Jun 25, 2026

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
18:10

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency

Published on: June 16, 2011

维斯纳病毒的抗原变异

J V Scott, L Stowring, A T Haase

    Cell
    |October 1, 1979
    PubMed
    概括
    此摘要是机器生成的。

    维斯纳病毒通过其糖蛋白基因的突变发生抗原变异,而不是重组. 这导致了独特的病毒变异,逃避宿主免疫反应.

    更多相关视频

    Propagating and Detecting an Infectious Molecular Clone of Maedi-visna Virus that Expresses Green Fluorescent Protein
    08:49

    Propagating and Detecting an Infectious Molecular Clone of Maedi-visna Virus that Expresses Green Fluorescent Protein

    Published on: October 9, 2011

    Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
    08:09

    Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope

    Published on: March 24, 2017

    相关实验视频

    Last Updated: Jun 25, 2026

    Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
    18:10

    Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency

    Published on: June 16, 2011

    Propagating and Detecting an Infectious Molecular Clone of Maedi-visna Virus that Expresses Green Fluorescent Protein
    08:49

    Propagating and Detecting an Infectious Molecular Clone of Maedi-visna Virus that Expresses Green Fluorescent Protein

    Published on: October 9, 2011

    Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
    08:09

    Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope

    Published on: March 24, 2017

    科学领域:

    • 病毒学 病毒学
    • 免疫学 免疫学 免疫学
    • 分子生物学分子生物学

    背景情况:

    • 维斯纳病毒导致绵羊慢慢,持久感染.
    • 抗原变异是lentiviruses免疫逃避的一个关键机制.

    研究的目的:

    • 研究维斯纳病毒抗原变异的遗传基础.
    • 要区分突变和重组作为变异生成的原因.

    主要方法:

    • 从受感染的绵羊中分离和表征序列抗原变异 (LV1-1,LV1-4).
    • 对包膜糖蛋白 (gp135) 和核心蛋白 (p30,p16,p14) 的图进行比较分析.
    • T1核糖核酶消化用于比较RNA寡核酸样本.

    主要成果:

    • 确定了两种不同的抗原变异,LV1-1和LV1-4.
    • 只有信封糖蛋白gp135在变体之间的图中显示了差异.
    • RNA图是相同的,只有gp135中的几个片段被改变.
    • 鉴定出gp135是产生中和抗体的免疫主导多.

    结论:

    • 维斯纳病毒糖蛋白基因内的突变是抗原变异的可能驱动因素.
    • 由于观察到其他病毒成分的遗传稳定性,再组合的可能性较小.
    • 了解这种机制对于开发有效的维斯纳病毒控制策略至关重要.