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Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein
Alpha-1-antitrypsin (AAT), an acute-phase protein encoded by the SERPINA1 gene, is a member of the serine protease inhibitor (SERPIN) superfamily. Its primary function is to protect tissues from enzymes released during inflammation, such as neutrophil elastase and proteinase 3. In addition to its an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731214/ https://www.ncbi.nlm.nih.gov/pubmed/33276468 http://dx.doi.org/10.3390/ijms21239187 |
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author | Lechowicz, Urszula Rudzinski, Stefan Jezela-Stanek, Aleksandra Janciauskiene, Sabina Chorostowska-Wynimko, Joanna |
author_facet | Lechowicz, Urszula Rudzinski, Stefan Jezela-Stanek, Aleksandra Janciauskiene, Sabina Chorostowska-Wynimko, Joanna |
author_sort | Lechowicz, Urszula |
collection | PubMed |
description | Alpha-1-antitrypsin (AAT), an acute-phase protein encoded by the SERPINA1 gene, is a member of the serine protease inhibitor (SERPIN) superfamily. Its primary function is to protect tissues from enzymes released during inflammation, such as neutrophil elastase and proteinase 3. In addition to its antiprotease activity, AAT interacts with numerous other substances and has various functions, mainly arising from the conformational flexibility of normal variants of AAT. Therefore, AAT has diverse biological functions and plays a role in various pathophysiological processes. This review discusses major molecular forms of AAT, including complex, cleaved, glycosylated, oxidized, and S-nitrosylated forms, in terms of their origin and function. |
format | Online Article Text |
id | pubmed-7731214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77312142020-12-12 Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein Lechowicz, Urszula Rudzinski, Stefan Jezela-Stanek, Aleksandra Janciauskiene, Sabina Chorostowska-Wynimko, Joanna Int J Mol Sci Review Alpha-1-antitrypsin (AAT), an acute-phase protein encoded by the SERPINA1 gene, is a member of the serine protease inhibitor (SERPIN) superfamily. Its primary function is to protect tissues from enzymes released during inflammation, such as neutrophil elastase and proteinase 3. In addition to its antiprotease activity, AAT interacts with numerous other substances and has various functions, mainly arising from the conformational flexibility of normal variants of AAT. Therefore, AAT has diverse biological functions and plays a role in various pathophysiological processes. This review discusses major molecular forms of AAT, including complex, cleaved, glycosylated, oxidized, and S-nitrosylated forms, in terms of their origin and function. MDPI 2020-12-02 /pmc/articles/PMC7731214/ /pubmed/33276468 http://dx.doi.org/10.3390/ijms21239187 Text en © 2020 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 | Review Lechowicz, Urszula Rudzinski, Stefan Jezela-Stanek, Aleksandra Janciauskiene, Sabina Chorostowska-Wynimko, Joanna Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein |
title | Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein |
title_full | Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein |
title_fullStr | Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein |
title_full_unstemmed | Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein |
title_short | Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein |
title_sort | post-translational modifications of circulating alpha-1-antitrypsin protein |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731214/ https://www.ncbi.nlm.nih.gov/pubmed/33276468 http://dx.doi.org/10.3390/ijms21239187 |
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