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Related Concept Videos

Antibody Structure and Classes01:25

Antibody Structure and Classes

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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.
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Antibody Structure01:10

Antibody Structure

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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...
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Cross-reactivity00:42

Cross-reactivity

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Antibody Actions01:26

Antibody Actions

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Antibodies, or immunoglobulins, are critical players in the immune system's arsenal against invading pathogens. Produced by B cells and plasma cells, their primary role is to detect and bind to specific antigens, molecules found on the surface of pathogens like bacteria or viruses. Beyond antigen recognition, antibodies perform several vital functions that contribute to immune defense.
Neutralization
Antibodies can bind to pathogens, preventing them from infecting host cells. This process...
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Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

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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...
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Affinity and Avidity01:41

Affinity and Avidity

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Updated: Aug 23, 2025

Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
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Antibody Class(es) Predictor for Epitopes (AbCPE): A Multi-Label Classification Algorithm.

Kiran Kadam1, Noor Peerzada2, Rajiv Karbhal1

  • 1Bioinformatics Centre, Savitribai Phule Pune University, Pune, India.

Frontiers in Bioinformatics
|October 28, 2022
PubMed
Summary
This summary is machine-generated.

A new algorithm, AbCPE, predicts which antibody classes (IgG, IgE, IgA, IgM) an epitope may bind to. This advances immunoinformatics and aids in developing targeted immunotherapies and vaccines.

Keywords:
antibodyantibody classantigen-antibody interactionbioinformaticsepitope predictionimmunoinformaticsmulti-label classificationmulti-specificity

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Area of Science:

  • Immunoinformatics
  • Synthetic Biology
  • Vaccine Development

Background:

  • Vaccine and antibody development are crucial for public health, with strategies evolving towards rational design.
  • Current B-cell epitope prediction methods often fail to account for antibody class specificity.
  • Multiple antibody classes can be associated with a single disease, necessitating class-specific prediction.

Purpose of the Study:

  • To develop a novel algorithm, AbCPE, for predicting antibody class(es) that a B-cell epitope can bind to.
  • To address the open problem of predicting 'peptidomes' that bind to multiple antibody classes.
  • To advance immunoinformatics by enabling class-specific epitope prediction.

Main Methods:

  • Developed AbCPE, a novel algorithm using a multi-label classification approach.
  • Utilized a knowledgebase of epitopes binding to IgG, IgE, IgA, and IgM antibodies.
  • Applied multi-label algorithms (Binary Relevance, Label Powerset) with Random Forest and AdaBoost classifiers.

Main Results:

  • The Binary Relevance model with Random Forest and AdaBoost achieved high performance.
  • Achieved a Hamming Loss of 0.1121 on training and 0.1074 on test sets.
  • Demonstrated promising results for antibody class prediction of sequential B-cell epitopes.

Conclusions:

  • AbCPE is the first multi-label method for predicting antibody class(es) for sequential B-cell epitopes.
  • The algorithm is expected to shift paradigms in immunoinformatics and immunotherapeutic development.
  • The AbCPE web server is available for public use, facilitating research and development.