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SERPINs—From Trap to Treatment
Excessive enzyme activity often has pathological consequences. This for example is the case in thrombosis and hereditary angioedema, where serine proteases of the coagulation system and kallikrein-kinin system are excessively active. Serine proteases are controlled by SERPINs (serine protease inhibi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379291/ https://www.ncbi.nlm.nih.gov/pubmed/30809526 http://dx.doi.org/10.3389/fmed.2019.00025 |
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author | Sanrattana, Wariya Maas, Coen de Maat, Steven |
author_facet | Sanrattana, Wariya Maas, Coen de Maat, Steven |
author_sort | Sanrattana, Wariya |
collection | PubMed |
description | Excessive enzyme activity often has pathological consequences. This for example is the case in thrombosis and hereditary angioedema, where serine proteases of the coagulation system and kallikrein-kinin system are excessively active. Serine proteases are controlled by SERPINs (serine protease inhibitors). We here describe the basic biochemical mechanisms behind SERPIN activity and identify key determinants that influence their function. We explore the clinical phenotypes of several SERPIN deficiencies and review studies where SERPINs are being used beyond replacement therapy. Excitingly, rare human SERPIN mutations have led us and others to believe that it is possible to refine SERPINs toward desired behavior for the treatment of enzyme-driven pathology. |
format | Online Article Text |
id | pubmed-6379291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63792912019-02-26 SERPINs—From Trap to Treatment Sanrattana, Wariya Maas, Coen de Maat, Steven Front Med (Lausanne) Medicine Excessive enzyme activity often has pathological consequences. This for example is the case in thrombosis and hereditary angioedema, where serine proteases of the coagulation system and kallikrein-kinin system are excessively active. Serine proteases are controlled by SERPINs (serine protease inhibitors). We here describe the basic biochemical mechanisms behind SERPIN activity and identify key determinants that influence their function. We explore the clinical phenotypes of several SERPIN deficiencies and review studies where SERPINs are being used beyond replacement therapy. Excitingly, rare human SERPIN mutations have led us and others to believe that it is possible to refine SERPINs toward desired behavior for the treatment of enzyme-driven pathology. Frontiers Media S.A. 2019-02-12 /pmc/articles/PMC6379291/ /pubmed/30809526 http://dx.doi.org/10.3389/fmed.2019.00025 Text en Copyright © 2019 Sanrattana, Maas and de Maat. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Sanrattana, Wariya Maas, Coen de Maat, Steven SERPINs—From Trap to Treatment |
title | SERPINs—From Trap to Treatment |
title_full | SERPINs—From Trap to Treatment |
title_fullStr | SERPINs—From Trap to Treatment |
title_full_unstemmed | SERPINs—From Trap to Treatment |
title_short | SERPINs—From Trap to Treatment |
title_sort | serpins—from trap to treatment |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379291/ https://www.ncbi.nlm.nih.gov/pubmed/30809526 http://dx.doi.org/10.3389/fmed.2019.00025 |
work_keys_str_mv | AT sanrattanawariya serpinsfromtraptotreatment AT maascoen serpinsfromtraptotreatment AT demaatsteven serpinsfromtraptotreatment |