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Related Concept Videos

Cross-reactivity00:42

Cross-reactivity

Overview
Antibody Structure01:10

Antibody Structure

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...
Antibody Structure01:10

Antibody Structure

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...
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.
Antibody Structure and Classes01:25

Antibody Structure and Classes

Antibodies, also known as immunoglobulins, are produced by B cells in response to foreign substances, such as bacteria and viruses. These proteins are critical for recognizing and neutralizing these substances, protecting the body from potential harm.
The basic structure of an antibody consists of four protein chains: two identical heavy chains and two identical light chains. These chains are held together by disulfide bonds and other non-covalent interactions, forming a Y-shaped structure.
Allergic Reactions02:06

Allergic Reactions

Overview

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Related Experiment Video

Updated: May 9, 2026

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
07:59

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes

Published on: March 25, 2014

Structure of allergens and structure based epitope predictions.

Fabio Dall'antonia1, Tea Pavkov-Keller2, Klaus Zangger3

  • 1European Molecular Biology Laboratory, Hamburg Outstation, Hamburg, Germany.

Methods (San Diego, Calif.)
|July 30, 2013
PubMed
Summary

Determining allergen structures is key to understanding epitopes. This review covers structural data, experimental methods, and computational approaches for epitope mapping, aiding allergy research.

Keywords:
Allergen structureIgE epitopeNMRProtein familyStructure based epitope predictionX-ray

Related Experiment Videos

Last Updated: May 9, 2026

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
07:59

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes

Published on: March 25, 2014

Area of Science:

  • Immunology
  • Structural Biology
  • Bioinformatics

Background:

  • Allergen structure determination is crucial for analyzing surface features and mapping epitopes.
  • Experimental methods like crystallography and NMR, alongside computational predictions, are used for this purpose.

Purpose of the Study:

  • To review existing structural information on allergens and their classification into protein fold families.
  • To describe available allergen-antibody complexes and compare experimentally obtained epitopes.
  • To discuss methods for linear and conformational epitope mapping, including a novel prediction approach.

Main Methods:

  • Literature review of structural data on allergens.
  • Analysis of crystallographic and NMR-based structural studies.
  • Description of computational epitope prediction methods, including structure-based approaches.

Main Results:

  • Summary of classified allergen protein fold families.
  • Compilation of available allergen-antibody complex structures.
  • Comparison of experimentally determined epitopes.
  • Discussion of established and novel epitope mapping techniques.

Conclusions:

  • Structural insights into allergens are fundamental for understanding allergic responses.
  • A combination of experimental and computational methods provides comprehensive epitope mapping.
  • New approaches integrating structural similarity and cross-reactivity data enhance epitope prediction accuracy.