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Novel insights into peptide amidation and amidating activity in the human circulation
C-terminal α-amidation is the final and essential step in the biosynthesis of several peptide hormones. Peptidylglycine α-amidating monooxygenase (PAM) is the only known enzyme to catalyse this reaction. PAM amidating activity (AMA) is known to be present in human circulation, but its physiological...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8338962/ https://www.ncbi.nlm.nih.gov/pubmed/34349173 http://dx.doi.org/10.1038/s41598-021-95305-y |
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author | Kaufmann, Paul Bergmann, Andreas Melander, Olle |
author_facet | Kaufmann, Paul Bergmann, Andreas Melander, Olle |
author_sort | Kaufmann, Paul |
collection | PubMed |
description | C-terminal α-amidation is the final and essential step in the biosynthesis of several peptide hormones. Peptidylglycine α-amidating monooxygenase (PAM) is the only known enzyme to catalyse this reaction. PAM amidating activity (AMA) is known to be present in human circulation, but its physiological role and significance as a clinical biomarker remains unclear. We developed a PAM-specific amidation assay that utilizes the naturally occurring substrate Adrenomedullin-Gly (ADM-Gly, 1–53). Using our amidation assay we quantified serum amidating activities in a large population-based cohort of more than 4900 individuals. A correlation of serum amidating activity with several clinical parameters including high blood pressure was observed. Increasing PAM-AMA was an independent predictor of hard outcomes related to hemodynamic stress such as cardiovascular mortality, atrial fibrillation and heart failure during long-term follow-up (8.8 ± 2.5 years). Moreover, results from an animal study in rats utilizing recombinant human PAM provide novel insights into the physiological role of circulating PAM and show its potential significance in circulating peptide amidation. |
format | Online Article Text |
id | pubmed-8338962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83389622021-08-05 Novel insights into peptide amidation and amidating activity in the human circulation Kaufmann, Paul Bergmann, Andreas Melander, Olle Sci Rep Article C-terminal α-amidation is the final and essential step in the biosynthesis of several peptide hormones. Peptidylglycine α-amidating monooxygenase (PAM) is the only known enzyme to catalyse this reaction. PAM amidating activity (AMA) is known to be present in human circulation, but its physiological role and significance as a clinical biomarker remains unclear. We developed a PAM-specific amidation assay that utilizes the naturally occurring substrate Adrenomedullin-Gly (ADM-Gly, 1–53). Using our amidation assay we quantified serum amidating activities in a large population-based cohort of more than 4900 individuals. A correlation of serum amidating activity with several clinical parameters including high blood pressure was observed. Increasing PAM-AMA was an independent predictor of hard outcomes related to hemodynamic stress such as cardiovascular mortality, atrial fibrillation and heart failure during long-term follow-up (8.8 ± 2.5 years). Moreover, results from an animal study in rats utilizing recombinant human PAM provide novel insights into the physiological role of circulating PAM and show its potential significance in circulating peptide amidation. Nature Publishing Group UK 2021-08-04 /pmc/articles/PMC8338962/ /pubmed/34349173 http://dx.doi.org/10.1038/s41598-021-95305-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kaufmann, Paul Bergmann, Andreas Melander, Olle Novel insights into peptide amidation and amidating activity in the human circulation |
title | Novel insights into peptide amidation and amidating activity in the human circulation |
title_full | Novel insights into peptide amidation and amidating activity in the human circulation |
title_fullStr | Novel insights into peptide amidation and amidating activity in the human circulation |
title_full_unstemmed | Novel insights into peptide amidation and amidating activity in the human circulation |
title_short | Novel insights into peptide amidation and amidating activity in the human circulation |
title_sort | novel insights into peptide amidation and amidating activity in the human circulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8338962/ https://www.ncbi.nlm.nih.gov/pubmed/34349173 http://dx.doi.org/10.1038/s41598-021-95305-y |
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