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The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms
In this review, we extensively describe the main post-translational modifications that give rise to the multiple proteoforms characterized to date in the human salivary proteome and their potential role. Most of the data reported were obtained by our group in over twenty-five years of research carri...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454625/ https://www.ncbi.nlm.nih.gov/pubmed/37628956 http://dx.doi.org/10.3390/ijms241612776 |
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author | Messana, Irene Manconi, Barbara Cabras, Tiziana Boroumand, Mozhgan Sanna, Maria Teresa Iavarone, Federica Olianas, Alessandra Desiderio, Claudia Rossetti, Diana Valeria Vincenzoni, Federica Contini, Cristina Guadalupi, Giulia Fiorita, Antonella Faa, Gavino Castagnola, Massimo |
author_facet | Messana, Irene Manconi, Barbara Cabras, Tiziana Boroumand, Mozhgan Sanna, Maria Teresa Iavarone, Federica Olianas, Alessandra Desiderio, Claudia Rossetti, Diana Valeria Vincenzoni, Federica Contini, Cristina Guadalupi, Giulia Fiorita, Antonella Faa, Gavino Castagnola, Massimo |
author_sort | Messana, Irene |
collection | PubMed |
description | In this review, we extensively describe the main post-translational modifications that give rise to the multiple proteoforms characterized to date in the human salivary proteome and their potential role. Most of the data reported were obtained by our group in over twenty-five years of research carried out on human saliva mainly by applying a top-down strategy. In the beginning, we describe the products generated by proteolytic cleavages, which can occur before and after secretion. In this section, the most relevant families of salivary proteins are also described. Next, we report the current information concerning the human salivary phospho-proteome and the limited news available on sulfo-proteomes. Three sections are dedicated to the description of glycation and enzymatic glycosylation. Citrullination and N- and C-terminal post-translational modifications (PTMs) and miscellaneous other modifications are described in the last two sections. Results highlighting the variation in the level of some proteoforms in local or systemic pathologies are also reviewed throughout the sections of the manuscript to underline the impact and relevance of this information for the development of new diagnostic biomarkers useful in clinical practice. |
format | Online Article Text |
id | pubmed-10454625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104546252023-08-26 The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms Messana, Irene Manconi, Barbara Cabras, Tiziana Boroumand, Mozhgan Sanna, Maria Teresa Iavarone, Federica Olianas, Alessandra Desiderio, Claudia Rossetti, Diana Valeria Vincenzoni, Federica Contini, Cristina Guadalupi, Giulia Fiorita, Antonella Faa, Gavino Castagnola, Massimo Int J Mol Sci Review In this review, we extensively describe the main post-translational modifications that give rise to the multiple proteoforms characterized to date in the human salivary proteome and their potential role. Most of the data reported were obtained by our group in over twenty-five years of research carried out on human saliva mainly by applying a top-down strategy. In the beginning, we describe the products generated by proteolytic cleavages, which can occur before and after secretion. In this section, the most relevant families of salivary proteins are also described. Next, we report the current information concerning the human salivary phospho-proteome and the limited news available on sulfo-proteomes. Three sections are dedicated to the description of glycation and enzymatic glycosylation. Citrullination and N- and C-terminal post-translational modifications (PTMs) and miscellaneous other modifications are described in the last two sections. Results highlighting the variation in the level of some proteoforms in local or systemic pathologies are also reviewed throughout the sections of the manuscript to underline the impact and relevance of this information for the development of new diagnostic biomarkers useful in clinical practice. MDPI 2023-08-14 /pmc/articles/PMC10454625/ /pubmed/37628956 http://dx.doi.org/10.3390/ijms241612776 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Messana, Irene Manconi, Barbara Cabras, Tiziana Boroumand, Mozhgan Sanna, Maria Teresa Iavarone, Federica Olianas, Alessandra Desiderio, Claudia Rossetti, Diana Valeria Vincenzoni, Federica Contini, Cristina Guadalupi, Giulia Fiorita, Antonella Faa, Gavino Castagnola, Massimo The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms |
title | The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms |
title_full | The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms |
title_fullStr | The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms |
title_full_unstemmed | The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms |
title_short | The Post-Translational Modifications of Human Salivary Peptides and Proteins Evidenced by Top-Down Platforms |
title_sort | post-translational modifications of human salivary peptides and proteins evidenced by top-down platforms |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454625/ https://www.ncbi.nlm.nih.gov/pubmed/37628956 http://dx.doi.org/10.3390/ijms241612776 |
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