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Related Concept Videos

Antigens Involved in Adaptive Immunity01:26

Antigens Involved in Adaptive Immunity

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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.
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MHC molecules are key players in the immune response, enabling T cells to recognize and respond to specific antigens. They are present on the surface of all nucleated cells in the body and are instrumental in presenting antigens to T cells and activating them. T cells recognize the MHC-antigen complex and initiate an immune response. MHC class I and MHC class II are two main types of MHC molecules, each associated with a distinct antigen processing pathway.
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Related Experiment Video

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

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Computational Resources for MHC Ligand Identification.

Christian P Koch1, Max Pillong1, Jan A Hiss1

  • 1ETH Zürich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Wolfgang-Pauli-Str. 10, 8093 Zürich, Switzerland.

Molecular Informatics
|August 3, 2016
PubMed
Summary
This summary is machine-generated.

Rational design of immunomodulatory peptides is now feasible due to advances in major histocompatibility complex (MHC) research and computational predictions. Proteome-derived peptides and computational vaccinology will drive future vaccine development.

Keywords:
BioinformaticsEpitopeImmunologyMajor histocompatibility complexPeptide designPredictionVaccine

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Immunopeptidomics: Isolation of Mouse and Human MHC Class I- and II-Associated Peptides for Mass Spectrometry Analysis
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Area of Science:

  • Immunology
  • Computational Biology
  • Biotechnology

Background:

  • Major histocompatibility complex (MHC) molecules present peptides to immune cells, mediating immune responses.
  • High-throughput screening and computational methods have advanced the identification of functional MHC modulators.
  • Rational design of immunomodulatory peptides is becoming increasingly feasible.

Purpose of the Study:

  • To review the molecular mechanisms of MHC-mediated immune responses.
  • To present emerging computational approaches in MHC ligand prediction and design.
  • To provide an overview of available computational resources for peptide design.

Main Methods:

  • Review of molecular mechanisms of MHC-mediated immunity.
  • Presentation of computational biotechnology approaches for MHC ligand prediction.
  • Compilation of publicly available computational resources.

Main Results:

  • Advances in high-throughput screening and computational prediction enable rational design of immunomodulatory peptides.
  • Proteome-derived peptides and computational 'reverse vaccinology' are key for future vaccine design.
  • A range of computational tools and resources are available for designing peptidic MHC ligands.

Conclusions:

  • The integration of high-throughput data and computational methods is revolutionizing immunomodulatory peptide design.
  • Computational approaches, including reverse vaccinology, are crucial for next-generation vaccine development.
  • Accessible computational resources facilitate the prediction and design of novel peptidic MHC ligands.