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The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin

Protein fibrillation is the pathological hallmark of several neurodegenerative diseases and also complicates the manufacturing and use of protein drugs. As a case study, the inhibitory activity of the natural compound aloin against insulin fibrillation was investigated. Based on Thioflavin T assays,...

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Autores principales: Lobbens, Eva S., Foderà, Vito, Nyberg, Nils T., Andersen, Kirsten, Jäger, Anna K., Jorgensen, Lene, van de Weert, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755604/
https://www.ncbi.nlm.nih.gov/pubmed/26882071
http://dx.doi.org/10.1371/journal.pone.0149148
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author Lobbens, Eva S.
Foderà, Vito
Nyberg, Nils T.
Andersen, Kirsten
Jäger, Anna K.
Jorgensen, Lene
van de Weert, Marco
author_facet Lobbens, Eva S.
Foderà, Vito
Nyberg, Nils T.
Andersen, Kirsten
Jäger, Anna K.
Jorgensen, Lene
van de Weert, Marco
author_sort Lobbens, Eva S.
collection PubMed
description Protein fibrillation is the pathological hallmark of several neurodegenerative diseases and also complicates the manufacturing and use of protein drugs. As a case study, the inhibitory activity of the natural compound aloin against insulin fibrillation was investigated. Based on Thioflavin T assays, high-performance liquid chromatography and transmission electron microscopy it was found that a degradation product of aloin, formed over weeks of storage, was able to significantly inhibit insulin fibrillation. The activity of the stored aloin was significantly reduced in the presence of small amounts of sodium azide or ascorbic acid, suggesting the active compound to be an oxidation product. A high-performance liquid chromatography method and a liquid chromatography-mass spectrometry method were developed to investigate the degradation products in the aged aloin solution. We found that the major compounds in the solution were aloin A and aloin B. In addition, 10-hydroxy aloin and elgonica dimers were detected in smaller amounts. The identified compounds were isolated and tested for activity by means of Thioflavin T assays, but no activity was observed. Thus, the actual fibrillation inhibitor is an as yet unidentified and potentially metastable degradation product of aloin. These results suggest that degradation products, and in particular oxidation products, are to be considered thoroughly when natural products are investigated for activity against protein fibrillation.
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spelling pubmed-47556042016-02-26 The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin Lobbens, Eva S. Foderà, Vito Nyberg, Nils T. Andersen, Kirsten Jäger, Anna K. Jorgensen, Lene van de Weert, Marco PLoS One Research Article Protein fibrillation is the pathological hallmark of several neurodegenerative diseases and also complicates the manufacturing and use of protein drugs. As a case study, the inhibitory activity of the natural compound aloin against insulin fibrillation was investigated. Based on Thioflavin T assays, high-performance liquid chromatography and transmission electron microscopy it was found that a degradation product of aloin, formed over weeks of storage, was able to significantly inhibit insulin fibrillation. The activity of the stored aloin was significantly reduced in the presence of small amounts of sodium azide or ascorbic acid, suggesting the active compound to be an oxidation product. A high-performance liquid chromatography method and a liquid chromatography-mass spectrometry method were developed to investigate the degradation products in the aged aloin solution. We found that the major compounds in the solution were aloin A and aloin B. In addition, 10-hydroxy aloin and elgonica dimers were detected in smaller amounts. The identified compounds were isolated and tested for activity by means of Thioflavin T assays, but no activity was observed. Thus, the actual fibrillation inhibitor is an as yet unidentified and potentially metastable degradation product of aloin. These results suggest that degradation products, and in particular oxidation products, are to be considered thoroughly when natural products are investigated for activity against protein fibrillation. Public Library of Science 2016-02-16 /pmc/articles/PMC4755604/ /pubmed/26882071 http://dx.doi.org/10.1371/journal.pone.0149148 Text en © 2016 Lobbens et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lobbens, Eva S.
Foderà, Vito
Nyberg, Nils T.
Andersen, Kirsten
Jäger, Anna K.
Jorgensen, Lene
van de Weert, Marco
The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin
title The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin
title_full The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin
title_fullStr The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin
title_full_unstemmed The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin
title_short The Inhibitory Effect of Natural Products on Protein Fibrillation May Be Caused by Degradation Products – A Study Using Aloin and Insulin
title_sort inhibitory effect of natural products on protein fibrillation may be caused by degradation products – a study using aloin and insulin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755604/
https://www.ncbi.nlm.nih.gov/pubmed/26882071
http://dx.doi.org/10.1371/journal.pone.0149148
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