Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

1.9K
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...
1.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Humans and rhesus macaques share maturation pathways of HIV-1 envelope-reactive V3-glycan bnAb lineages.

Science translational medicine·2026
Same author

Enhanced B cell priming induces broadly neutralizing HIV-1 apex antibodies.

Nature·2026
Same author

Genotypic challenges in implementing broadly neutralizing antibody-based long-acting HIV-1 therapies.

Communications medicine·2026
Same author

Induction of broadly neutralizing HIV antibodies by a two-step mechanism informs vaccine design.

Science (New York, N.Y.)·2026
Same author

Contemporary HIV-1 envelope pseudovirus panels for detecting and assessing B cell lineages with broadly neutralizing antibody potential.

PLoS pathogens·2026
Same author

Env-antibody coevolution identifies B cell priming as the principal bottleneck to HIV V2 apex broadly neutralizing antibody development.

Science immunology·2026

Related Experiment Video

Updated: Mar 8, 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

15.7K

Graph-based optimization of epitope coverage for vaccine antigen design.

James Theiler1,2, Bette Korber1,2

  • 1Los Alamos National Laboratory, Los Alamos, 87545, NM, U.S.A.

Statistics in Medicine
|January 30, 2017
PubMed
Summary

Epigraph is a new algorithm for designing vaccines that maximize epitope coverage in diverse pathogens. It aids in rapid characterization of pathogen sequences and designing peptides for immune response evaluation.

Keywords:
algorithmantigende Bruijn graphdirected acyclic graphepitopevaccine

More Related Videos

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

10.1K
Overlapping Peptide Library to Map Qa-1 Epitopes in a Protein
08:04

Overlapping Peptide Library to Map Qa-1 Epitopes in a Protein

Published on: December 20, 2017

7.4K

Related Experiment Videos

Last Updated: Mar 8, 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

15.7K
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

10.1K
Overlapping Peptide Library to Map Qa-1 Epitopes in a Protein
08:04

Overlapping Peptide Library to Map Qa-1 Epitopes in a Protein

Published on: December 20, 2017

7.4K

Area of Science:

  • Computational biology
  • Vaccine design
  • Immunoinformatics

Background:

  • Designing vaccines against diverse pathogens requires maximizing epitope coverage.
  • Existing methods may not efficiently handle large, diverse sequence populations.
  • Understanding immune responses to variable proteins is crucial.

Purpose of the Study:

  • To introduce Epigraph, a computationally efficient algorithm for vaccine design.
  • To describe the mathematical formulation of Epigraph for optimal epitope coverage.
  • To present tools for characterizing pathogen populations and designing experimental peptides.

Main Methods:

  • Formulating the optimal coverage problem as a directed graph.
  • Representing candidate antigens as paths traversing the graph.
  • Utilizing immunologically relevant shared potential epitope frequencies for distance measures.

Main Results:

  • Epigraph enables efficient design of single or multi-antigen vaccines.
  • The Epigraph tool suite allows rapid characterization of diverse sequence populations.
  • New tools provide frequency summaries of distinct potential epitopes and graphical outputs.

Conclusions:

  • Epigraph offers a novel approach to vaccine design by optimizing epitope coverage.
  • The associated tool suite facilitates immunological characterization and experimental peptide design.
  • Epigraph provides valuable insights into pathogen diversity and vaccine strategies.