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N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals

Hemocyanins are widely used as carriers, adjuvants, and nonspecific immunostimulants in cancer because they promote Th1 immunity in mammals. Hemocyanins also interact with glycan-recognizing innate immune receptors on antigen-presenting cells, such as the C-type lectin immune receptors mannose recep...

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Autores principales: Salazar, Michelle L., Jiménez, José M., Villar, Javiera, Rivera, Maira, Báez, Mauricio, Manubens, Augusto, Becker, María Inés
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926458/
https://www.ncbi.nlm.nih.gov/pubmed/31719148
http://dx.doi.org/10.1074/jbc.RA119.009525
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author Salazar, Michelle L.
Jiménez, José M.
Villar, Javiera
Rivera, Maira
Báez, Mauricio
Manubens, Augusto
Becker, María Inés
author_facet Salazar, Michelle L.
Jiménez, José M.
Villar, Javiera
Rivera, Maira
Báez, Mauricio
Manubens, Augusto
Becker, María Inés
author_sort Salazar, Michelle L.
collection PubMed
description Hemocyanins are widely used as carriers, adjuvants, and nonspecific immunostimulants in cancer because they promote Th1 immunity in mammals. Hemocyanins also interact with glycan-recognizing innate immune receptors on antigen-presenting cells, such as the C-type lectin immune receptors mannose receptor (MR), macrophage galactose lectin (MGL), and the Toll-like receptors (TLRs), stimulating proinflammatory cytokine secretion. However, the role of N-linked oligosaccharides on the structural and immunological properties of hemocyanin is unclear. Mollusk hemocyanins, such as Concholepas concholepas (CCH), Fissurella latimarginata (FLH), and Megathura crenulata (KLH), are oligomeric glycoproteins with complex dodecameric quaternary structures and heterogeneous glycosylation patterns, primarily consisting of mannose-rich N-glycans. Here, we report that enzyme-catalyzed N-deglycosylation of CCH, FLH, and KLH disrupts their quaternary structure and impairs their immunogenic effects. Biochemical analyses revealed that the deglycosylation does not change hemocyanin secondary structure but alters their refolding mechanism and dodecameric structure. Immunochemical analyses indicated decreased binding of N-deglycosylated hemocyanins to the MR and MGL receptors and TLR4 and reduced endocytosis concomitant with an impaired production of tumor necrosis factor α, and interleukins 6 and 12 (IL-6 and IL-12p40, respectively) in macrophages. Evaluating the function of N-deglycosylated hemocyanins in the humoral immune response and their nonspecific antitumor effects in the B16F10 melanoma model, we found that compared with native hemocyanins N-deglycosylated hemocyanins elicited reduced antibody titers, as well as partially diminished antitumor effects and altered carrier activities. In conclusion, the glycan content of hemocyanins is, among other structural characteristics, critically required for their immunological activities and should be considered in biomedical applications.
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spelling pubmed-69264582019-12-24 N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals Salazar, Michelle L. Jiménez, José M. Villar, Javiera Rivera, Maira Báez, Mauricio Manubens, Augusto Becker, María Inés J Biol Chem Immunology Hemocyanins are widely used as carriers, adjuvants, and nonspecific immunostimulants in cancer because they promote Th1 immunity in mammals. Hemocyanins also interact with glycan-recognizing innate immune receptors on antigen-presenting cells, such as the C-type lectin immune receptors mannose receptor (MR), macrophage galactose lectin (MGL), and the Toll-like receptors (TLRs), stimulating proinflammatory cytokine secretion. However, the role of N-linked oligosaccharides on the structural and immunological properties of hemocyanin is unclear. Mollusk hemocyanins, such as Concholepas concholepas (CCH), Fissurella latimarginata (FLH), and Megathura crenulata (KLH), are oligomeric glycoproteins with complex dodecameric quaternary structures and heterogeneous glycosylation patterns, primarily consisting of mannose-rich N-glycans. Here, we report that enzyme-catalyzed N-deglycosylation of CCH, FLH, and KLH disrupts their quaternary structure and impairs their immunogenic effects. Biochemical analyses revealed that the deglycosylation does not change hemocyanin secondary structure but alters their refolding mechanism and dodecameric structure. Immunochemical analyses indicated decreased binding of N-deglycosylated hemocyanins to the MR and MGL receptors and TLR4 and reduced endocytosis concomitant with an impaired production of tumor necrosis factor α, and interleukins 6 and 12 (IL-6 and IL-12p40, respectively) in macrophages. Evaluating the function of N-deglycosylated hemocyanins in the humoral immune response and their nonspecific antitumor effects in the B16F10 melanoma model, we found that compared with native hemocyanins N-deglycosylated hemocyanins elicited reduced antibody titers, as well as partially diminished antitumor effects and altered carrier activities. In conclusion, the glycan content of hemocyanins is, among other structural characteristics, critically required for their immunological activities and should be considered in biomedical applications. American Society for Biochemistry and Molecular Biology 2019-12-20 2019-11-12 /pmc/articles/PMC6926458/ /pubmed/31719148 http://dx.doi.org/10.1074/jbc.RA119.009525 Text en © 2019 Salazar et al. Author's Choice—Final version open access under the terms of the Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) .
spellingShingle Immunology
Salazar, Michelle L.
Jiménez, José M.
Villar, Javiera
Rivera, Maira
Báez, Mauricio
Manubens, Augusto
Becker, María Inés
N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
title N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
title_full N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
title_fullStr N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
title_full_unstemmed N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
title_short N-Glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
title_sort n-glycosylation of mollusk hemocyanins contributes to their structural stability and immunomodulatory properties in mammals
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6926458/
https://www.ncbi.nlm.nih.gov/pubmed/31719148
http://dx.doi.org/10.1074/jbc.RA119.009525
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