Cargando…

Joint epitope selection and spacer design for string-of-beads vaccines

MOTIVATION: Conceptually, epitope-based vaccine design poses two distinct problems: (i) selecting the best epitopes to elicit the strongest possible immune response and (ii) arranging and linking them through short spacer sequences to string-of-beads vaccines, so that their recovery likelihood durin...

Descripción completa

Detalles Bibliográficos
Autores principales: Dorigatti, Emilio, Schubert, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773482/
https://www.ncbi.nlm.nih.gov/pubmed/33381831
http://dx.doi.org/10.1093/bioinformatics/btaa790
_version_ 1783630054755926016
author Dorigatti, Emilio
Schubert, Benjamin
author_facet Dorigatti, Emilio
Schubert, Benjamin
author_sort Dorigatti, Emilio
collection PubMed
description MOTIVATION: Conceptually, epitope-based vaccine design poses two distinct problems: (i) selecting the best epitopes to elicit the strongest possible immune response and (ii) arranging and linking them through short spacer sequences to string-of-beads vaccines, so that their recovery likelihood during antigen processing is maximized. Current state-of-the-art approaches solve this design problem sequentially. Consequently, such approaches are unable to capture the inter-dependencies between the two design steps, usually emphasizing theoretical immunogenicity over correct vaccine processing, thus resulting in vaccines with less effective immunogenicity in vivo. RESULTS: In this work, we present a computational approach based on linear programming, called JessEV, that solves both design steps simultaneously, allowing to weigh the selection of a set of epitopes that have great immunogenic potential against their assembly into a string-of-beads construct that provides a high chance of recovery. We conducted Monte Carlo cleavage simulations to show that a fixed set of epitopes often cannot be assembled adequately, whereas selecting epitopes to accommodate proper cleavage requirements substantially improves their recovery probability and thus the effective immunogenicity, pathogen and population coverage of the resulting vaccines by at least 2-fold. AVAILABILITY AND IMPLEMENTATION: The software and the data analyzed are available at https://github.com/SchubertLab/JessEV. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
format Online
Article
Text
id pubmed-7773482
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77734822021-01-05 Joint epitope selection and spacer design for string-of-beads vaccines Dorigatti, Emilio Schubert, Benjamin Bioinformatics Genomes MOTIVATION: Conceptually, epitope-based vaccine design poses two distinct problems: (i) selecting the best epitopes to elicit the strongest possible immune response and (ii) arranging and linking them through short spacer sequences to string-of-beads vaccines, so that their recovery likelihood during antigen processing is maximized. Current state-of-the-art approaches solve this design problem sequentially. Consequently, such approaches are unable to capture the inter-dependencies between the two design steps, usually emphasizing theoretical immunogenicity over correct vaccine processing, thus resulting in vaccines with less effective immunogenicity in vivo. RESULTS: In this work, we present a computational approach based on linear programming, called JessEV, that solves both design steps simultaneously, allowing to weigh the selection of a set of epitopes that have great immunogenic potential against their assembly into a string-of-beads construct that provides a high chance of recovery. We conducted Monte Carlo cleavage simulations to show that a fixed set of epitopes often cannot be assembled adequately, whereas selecting epitopes to accommodate proper cleavage requirements substantially improves their recovery probability and thus the effective immunogenicity, pathogen and population coverage of the resulting vaccines by at least 2-fold. AVAILABILITY AND IMPLEMENTATION: The software and the data analyzed are available at https://github.com/SchubertLab/JessEV. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2020-12-29 /pmc/articles/PMC7773482/ /pubmed/33381831 http://dx.doi.org/10.1093/bioinformatics/btaa790 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genomes
Dorigatti, Emilio
Schubert, Benjamin
Joint epitope selection and spacer design for string-of-beads vaccines
title Joint epitope selection and spacer design for string-of-beads vaccines
title_full Joint epitope selection and spacer design for string-of-beads vaccines
title_fullStr Joint epitope selection and spacer design for string-of-beads vaccines
title_full_unstemmed Joint epitope selection and spacer design for string-of-beads vaccines
title_short Joint epitope selection and spacer design for string-of-beads vaccines
title_sort joint epitope selection and spacer design for string-of-beads vaccines
topic Genomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773482/
https://www.ncbi.nlm.nih.gov/pubmed/33381831
http://dx.doi.org/10.1093/bioinformatics/btaa790
work_keys_str_mv AT dorigattiemilio jointepitopeselectionandspacerdesignforstringofbeadsvaccines
AT schubertbenjamin jointepitopeselectionandspacerdesignforstringofbeadsvaccines