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Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

550
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...
550
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

693
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
693
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

1.7K
The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
1.7K
Antibody Structure01:10

Antibody Structure

59.6K
Overview
Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
The Y-Shaped Structure of Antibodies Consists of Four Polypeptide Chains
Antibodies consist of four polypeptide chains: two identical heavy...
59.6K
Assembly of Signaling Complexes01:30

Assembly of Signaling Complexes

5.7K
Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
5.7K
Activation and Inactivation of G Proteins01:22

Activation and Inactivation of G Proteins

6.9K
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high...
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  2. 完全に組み立てられた Γδ T細胞抗原受容体の構造
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  2. 完全に組み立てられた Γδ T細胞抗原受容体の構造

関連する実験動画

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
08:48

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain

Published on: October 25, 2016

8.5K

完全に組み立てられた γδ T細胞抗原受容体の構造

Benjamin S Gully1, João Ferreira Fernandes2,3, Sachith D Gunasinghe1

  • 1Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.

Nature
|August 15, 2024

PubMed で要約を見る

まとめ
この要約は機械生成です。

ガンマ・デルタT細胞受容体 (TCR) の構造が決定され,CD3サブユニット組織が保存されているが,アルファ・ベータTCRと比較してユニークな柔軟性があることが明らかになった. この構造的可塑性により,ガンマ・デルタ型TCRは,信号伝達能力を維持しながら,多様なリガンドを認識することができます.

さらに関連する動画

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins
16:10

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins

Published on: March 22, 2012

23.8K
Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens
09:53

Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens

Published on: February 6, 2017

11.4K

関連する実験動画

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain
08:48

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain

Published on: October 25, 2016

8.5K
A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins
16:10

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins

Published on: March 22, 2012

23.8K
Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens
09:53

Using X-ray Crystallography, Biophysics, and Functional Assays to Determine the Mechanisms Governing T-cell Receptor Recognition of Cancer Antigens

Published on: February 6, 2017

11.4K

科学分野:

  • 免疫学
  • 構造生物学
  • 分子生物学

背景:

  • 適応免疫に不可欠なT細胞は,T細胞受容体 (TCR) によって区別されるαβおよびγδ系統として存在します.
  • αβ T細胞受容体の構造はよく特徴づけられているが,γδ T細胞受容体の構造は不明である.
  • γδ T細胞受容体は,αβ T細胞受容体よりも幅広いリガンドを認識することが知られており,ユニークな構造的特性を示唆している.

研究 の 目的:

  • 人間の γδ T 細胞受容体の3次元構造を決定する.
  • γδ TCR の構造的組織と柔軟性を,既知の αβ TCR 構造と比較する.
  • γδ TCR構造が,その多様な結合能力とシグナル伝達機能とどのように関係しているかを理解する.

主な方法:

  • 組立したヒトVγ8Vδ3 TCR- CD3複合体を視覚化するために,冷凍電子顕微鏡 (cryo- EM) が使用された.
  • この複合体は,MR1および抗CD3ε抗体の断片と併用して研究された.
  • 構造分析は,TCR変数領域と保存されたCD3サブユニットの配置と相互作用に焦点を当てた.

主要な成果:

  • この研究では,ヒトの γδ TCR- CD3 複合体の構造を決定し,αβ TCR に類似した保存された CD3 亜単位の配置を明らかにした.
  • 硬質のαβ TCRとは異なり,γδ TCRは,トランスメブランヘリックス・テザリングにより,著しい形状の異質性を示した.
  • γδ TCRをαβ TCR構造に似ているように変更することで,リガンドの多様性とシグナリング効率の間のトレードオフを示します.
  • 結論:

    • γδ TCR構造は驚くべき可塑性を示し,多様なリガンド認識に対応する柔軟性を発揮する.
    • この構造的適応性は, γδ T 細胞が異なる免疫学的役割を果たすための重要な進化的特徴である.
    • この発見は,TCRを,硬体と柔軟な構造の両方を通してシグナルを送信できる多用途受容体として再定義します.