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Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36

The currently available nonavalent human papillomavirus (HPV) vaccine exploits the highly antigenic L1 major capsid protein to promote high-titer neutralizing antibodies, but is limited to the HPV types included in the vaccine since the responses are highly type-specific. The limited cross-protectio...

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Autores principales: Bywaters, Stephanie M., Brendle, Sarah A., Tossi, Kerstin P., Biryukov, Jennifer, Meyers, Craig, Christensen, Neil D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707543/
https://www.ncbi.nlm.nih.gov/pubmed/29125554
http://dx.doi.org/10.3390/v9110336
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author Bywaters, Stephanie M.
Brendle, Sarah A.
Tossi, Kerstin P.
Biryukov, Jennifer
Meyers, Craig
Christensen, Neil D.
author_facet Bywaters, Stephanie M.
Brendle, Sarah A.
Tossi, Kerstin P.
Biryukov, Jennifer
Meyers, Craig
Christensen, Neil D.
author_sort Bywaters, Stephanie M.
collection PubMed
description The currently available nonavalent human papillomavirus (HPV) vaccine exploits the highly antigenic L1 major capsid protein to promote high-titer neutralizing antibodies, but is limited to the HPV types included in the vaccine since the responses are highly type-specific. The limited cross-protection offered by the L1 virus-like particle (VLP) vaccine warrants further investigation into cross-protective L2 epitopes. The L2 proteins are yet to be fully characterized as to their precise placement in the virion. Adding to the difficulties in localizing L2, studies have suggested that L2 epitopes are not well exposed on the surface of the mature capsid prior to cellular engagement. Using a series of competition assays between previously mapped anti-L1 monoclonal antibodies (mAbs) (H16.V5, H16.U4 and H16.7E) and novel anti-L2 mAbs, we probed the capsid surface for the location of an L2 epitope (aa17–36). The previously characterized L1 epitopes together with our competition data is consistent with a proposed L2 epitope within the canyons of pentavalent capsomers.
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spelling pubmed-57075432017-12-05 Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36 Bywaters, Stephanie M. Brendle, Sarah A. Tossi, Kerstin P. Biryukov, Jennifer Meyers, Craig Christensen, Neil D. Viruses Article The currently available nonavalent human papillomavirus (HPV) vaccine exploits the highly antigenic L1 major capsid protein to promote high-titer neutralizing antibodies, but is limited to the HPV types included in the vaccine since the responses are highly type-specific. The limited cross-protection offered by the L1 virus-like particle (VLP) vaccine warrants further investigation into cross-protective L2 epitopes. The L2 proteins are yet to be fully characterized as to their precise placement in the virion. Adding to the difficulties in localizing L2, studies have suggested that L2 epitopes are not well exposed on the surface of the mature capsid prior to cellular engagement. Using a series of competition assays between previously mapped anti-L1 monoclonal antibodies (mAbs) (H16.V5, H16.U4 and H16.7E) and novel anti-L2 mAbs, we probed the capsid surface for the location of an L2 epitope (aa17–36). The previously characterized L1 epitopes together with our competition data is consistent with a proposed L2 epitope within the canyons of pentavalent capsomers. MDPI 2017-11-10 /pmc/articles/PMC5707543/ /pubmed/29125554 http://dx.doi.org/10.3390/v9110336 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bywaters, Stephanie M.
Brendle, Sarah A.
Tossi, Kerstin P.
Biryukov, Jennifer
Meyers, Craig
Christensen, Neil D.
Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36
title Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36
title_full Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36
title_fullStr Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36
title_full_unstemmed Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36
title_short Antibody Competition Reveals Surface Location of HPV L2 Minor Capsid Protein Residues 17–36
title_sort antibody competition reveals surface location of hpv l2 minor capsid protein residues 17–36
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707543/
https://www.ncbi.nlm.nih.gov/pubmed/29125554
http://dx.doi.org/10.3390/v9110336
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