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Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD)
We developed a new phage-display based approach, the Large Fragment Phage Display (LFPD), that can be used for mapping conformational epitopes on target molecules of immunological interest. LFPD uses a simplified and more effective phage-display approach in which only a limited set of larger fragmen...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610777/ https://www.ncbi.nlm.nih.gov/pubmed/23555577 http://dx.doi.org/10.1371/journal.pone.0058358 |
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author | Gabrielli, Federico Salvi, Roberto Garulli, Chiara Kalogris, Cristina Arima, Serena Tardella, Luca Monaci, Paolo Pupa, Serenella M. Tagliabue, Elda Montani, Maura Quaglino, Elena Stramucci, Lorenzo Curcio, Claudia Marchini, Cristina Amici, Augusto |
author_facet | Gabrielli, Federico Salvi, Roberto Garulli, Chiara Kalogris, Cristina Arima, Serena Tardella, Luca Monaci, Paolo Pupa, Serenella M. Tagliabue, Elda Montani, Maura Quaglino, Elena Stramucci, Lorenzo Curcio, Claudia Marchini, Cristina Amici, Augusto |
author_sort | Gabrielli, Federico |
collection | PubMed |
description | We developed a new phage-display based approach, the Large Fragment Phage Display (LFPD), that can be used for mapping conformational epitopes on target molecules of immunological interest. LFPD uses a simplified and more effective phage-display approach in which only a limited set of larger fragments (about 100 aa in length) are expressed on the phage surface. Using the human HER2 oncoprotein as a target, we identified novel B-cell conformational epitopes. The same homologous epitopes were also detected in rat HER2 and all corresponded to the epitopes predicted by computational analysis (PEPITO software), showing that LFPD gives reproducible and accurate results. Interestingly, these newly identified HER2 epitopes seem to be crucial for an effective immune response against HER2-overexpressing breast cancers and might help discriminating between metastatic breast cancer and early breast cancer patients. Overall, the results obtained in this study demonstrated the utility of LFPD and its potential application to the detection of conformational epitopes on many other molecules of interest, as well as, the development of new and potentially more effective B-cell conformational epitopes based vaccines. |
format | Online Article Text |
id | pubmed-3610777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36107772013-04-03 Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) Gabrielli, Federico Salvi, Roberto Garulli, Chiara Kalogris, Cristina Arima, Serena Tardella, Luca Monaci, Paolo Pupa, Serenella M. Tagliabue, Elda Montani, Maura Quaglino, Elena Stramucci, Lorenzo Curcio, Claudia Marchini, Cristina Amici, Augusto PLoS One Research Article We developed a new phage-display based approach, the Large Fragment Phage Display (LFPD), that can be used for mapping conformational epitopes on target molecules of immunological interest. LFPD uses a simplified and more effective phage-display approach in which only a limited set of larger fragments (about 100 aa in length) are expressed on the phage surface. Using the human HER2 oncoprotein as a target, we identified novel B-cell conformational epitopes. The same homologous epitopes were also detected in rat HER2 and all corresponded to the epitopes predicted by computational analysis (PEPITO software), showing that LFPD gives reproducible and accurate results. Interestingly, these newly identified HER2 epitopes seem to be crucial for an effective immune response against HER2-overexpressing breast cancers and might help discriminating between metastatic breast cancer and early breast cancer patients. Overall, the results obtained in this study demonstrated the utility of LFPD and its potential application to the detection of conformational epitopes on many other molecules of interest, as well as, the development of new and potentially more effective B-cell conformational epitopes based vaccines. Public Library of Science 2013-03-28 /pmc/articles/PMC3610777/ /pubmed/23555577 http://dx.doi.org/10.1371/journal.pone.0058358 Text en © 2013 Gabrielli et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gabrielli, Federico Salvi, Roberto Garulli, Chiara Kalogris, Cristina Arima, Serena Tardella, Luca Monaci, Paolo Pupa, Serenella M. Tagliabue, Elda Montani, Maura Quaglino, Elena Stramucci, Lorenzo Curcio, Claudia Marchini, Cristina Amici, Augusto Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) |
title | Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) |
title_full | Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) |
title_fullStr | Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) |
title_full_unstemmed | Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) |
title_short | Identification of Relevant Conformational Epitopes on the HER2 Oncoprotein by Using Large Fragment Phage Display (LFPD) |
title_sort | identification of relevant conformational epitopes on the her2 oncoprotein by using large fragment phage display (lfpd) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610777/ https://www.ncbi.nlm.nih.gov/pubmed/23555577 http://dx.doi.org/10.1371/journal.pone.0058358 |
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