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Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate

Tentacle‐like polymers decorated with several copies of peptide antigens can be interesting tools for increasing the ability to capture circulating antibodies in patient sera, using cooperative effects for stronger avidity. We previously showed that antibodies from multiple sclerosis (MS) patient se...

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Autores principales: Mazzoleni, Antonio, Real‐Fernandez, Feliciana, Nuti, Francesca, Lanzillo, Roberta, Brescia Morra, Vincenzo, Dambruoso, Paolo, Bertoldo, Monica, Rovero, Paolo, Mallet, Jean‐Maurice, Papini, Anna Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300045/
https://www.ncbi.nlm.nih.gov/pubmed/34761861
http://dx.doi.org/10.1002/cbic.202100515
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author Mazzoleni, Antonio
Real‐Fernandez, Feliciana
Nuti, Francesca
Lanzillo, Roberta
Brescia Morra, Vincenzo
Dambruoso, Paolo
Bertoldo, Monica
Rovero, Paolo
Mallet, Jean‐Maurice
Papini, Anna Maria
author_facet Mazzoleni, Antonio
Real‐Fernandez, Feliciana
Nuti, Francesca
Lanzillo, Roberta
Brescia Morra, Vincenzo
Dambruoso, Paolo
Bertoldo, Monica
Rovero, Paolo
Mallet, Jean‐Maurice
Papini, Anna Maria
author_sort Mazzoleni, Antonio
collection PubMed
description Tentacle‐like polymers decorated with several copies of peptide antigens can be interesting tools for increasing the ability to capture circulating antibodies in patient sera, using cooperative effects for stronger avidity. We previously showed that antibodies from multiple sclerosis (MS) patient sera preferentially recognize hyperglucosylated adhesin protein HMW1ct of non‐typeable Haemophilus influenzae (NTHi). We selected the C‐terminal HMW1ct(1347–1354) minimal epitope and prepared the diglucosylated analogue Ac‐KAN(Glc)VTLN(Glc)TTG‐K(N(3))‐NH(2) to graft a 40 kDa dextran scaffold modified with glycidyl‐propargyl moieties to perform a copper catalyzed alkyne‐azide coupling reaction (CuAAC). Quantitative NMR measurements allowed the characterization of the peptide loading (19.5 %) on the multivalent dextran conjugate. This novel polymeric structure displayed optimal capturing properties of both IgG and, more interestingly, IgM antibodies in MS sera. Specific antibodies from a representative MS serum, were successfully depleted using a Sepharose resin bearing the new glucosylated multivalent conjugate, as confirmed by ELISA. These results may offer a promising proof‐of‐concept for the selective purification of high affinity autoantibodies from sera of autoimmune patients, in general, and of specific high affinity antibodies against a minimally glcosylated epitope Asn(Glc) from sera of multiple sclerosis (MS) patients, in particular.
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spelling pubmed-93000452022-07-21 Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate Mazzoleni, Antonio Real‐Fernandez, Feliciana Nuti, Francesca Lanzillo, Roberta Brescia Morra, Vincenzo Dambruoso, Paolo Bertoldo, Monica Rovero, Paolo Mallet, Jean‐Maurice Papini, Anna Maria Chembiochem Full Papers Tentacle‐like polymers decorated with several copies of peptide antigens can be interesting tools for increasing the ability to capture circulating antibodies in patient sera, using cooperative effects for stronger avidity. We previously showed that antibodies from multiple sclerosis (MS) patient sera preferentially recognize hyperglucosylated adhesin protein HMW1ct of non‐typeable Haemophilus influenzae (NTHi). We selected the C‐terminal HMW1ct(1347–1354) minimal epitope and prepared the diglucosylated analogue Ac‐KAN(Glc)VTLN(Glc)TTG‐K(N(3))‐NH(2) to graft a 40 kDa dextran scaffold modified with glycidyl‐propargyl moieties to perform a copper catalyzed alkyne‐azide coupling reaction (CuAAC). Quantitative NMR measurements allowed the characterization of the peptide loading (19.5 %) on the multivalent dextran conjugate. This novel polymeric structure displayed optimal capturing properties of both IgG and, more interestingly, IgM antibodies in MS sera. Specific antibodies from a representative MS serum, were successfully depleted using a Sepharose resin bearing the new glucosylated multivalent conjugate, as confirmed by ELISA. These results may offer a promising proof‐of‐concept for the selective purification of high affinity autoantibodies from sera of autoimmune patients, in general, and of specific high affinity antibodies against a minimally glcosylated epitope Asn(Glc) from sera of multiple sclerosis (MS) patients, in particular. John Wiley and Sons Inc. 2021-12-06 2022-02-04 /pmc/articles/PMC9300045/ /pubmed/34761861 http://dx.doi.org/10.1002/cbic.202100515 Text en © 2021 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Mazzoleni, Antonio
Real‐Fernandez, Feliciana
Nuti, Francesca
Lanzillo, Roberta
Brescia Morra, Vincenzo
Dambruoso, Paolo
Bertoldo, Monica
Rovero, Paolo
Mallet, Jean‐Maurice
Papini, Anna Maria
Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate
title Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate
title_full Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate
title_fullStr Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate
title_full_unstemmed Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate
title_short Selective Capture of Anti‐N‐glucosylated NTHi Adhesin Peptide Antibodies by a Multivalent Dextran Conjugate
title_sort selective capture of anti‐n‐glucosylated nthi adhesin peptide antibodies by a multivalent dextran conjugate
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300045/
https://www.ncbi.nlm.nih.gov/pubmed/34761861
http://dx.doi.org/10.1002/cbic.202100515
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