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Differences in interaction lead to the formation of different types of insulin amyloid
Insulin balls, localized insulin amyloids formed at the site of repeated insulin injections in patients with diabetes, cause poor glycemic control and cytotoxicity. Our previous study has shown that insulin forms two types of amyloids; toxic amyloid formed from the intact insulin ((i)-amyloid) and l...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123177/ https://www.ncbi.nlm.nih.gov/pubmed/35595809 http://dx.doi.org/10.1038/s41598-022-12212-6 |
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author | Mori, Wakako Kawakami, Ryosuke Niko, Yosuke Haruta, Tomohiro Imamura, Takeshi Shiraki, Kentaro Zako, Tamotsu |
author_facet | Mori, Wakako Kawakami, Ryosuke Niko, Yosuke Haruta, Tomohiro Imamura, Takeshi Shiraki, Kentaro Zako, Tamotsu |
author_sort | Mori, Wakako |
collection | PubMed |
description | Insulin balls, localized insulin amyloids formed at the site of repeated insulin injections in patients with diabetes, cause poor glycemic control and cytotoxicity. Our previous study has shown that insulin forms two types of amyloids; toxic amyloid formed from the intact insulin ((i)-amyloid) and less-toxic amyloid formed in the presence of the reducing reagent TCEP ((r)-amyloid), suggesting insulin amyloid polymorphism. However, the differences in the formation mechanism and cytotoxicity expression are still unclear. Herein, we demonstrate that the liquid droplets, which are stabilized by electrostatic interactions, appear only in the process of toxic (i)-amyloid formation, but not in the less-toxic (r)-amyloid formation process. The effect of various additives such as arginine, 1,6-hexanediol, and salts on amyloid formation was also examined to investigate interactions that are important for amyloid formation. Our results indicate that the maturation processes of these two amyloids were significantly different, whereas the nucleation by hydrophobic interactions was similar. These results also suggest the difference in the formation mechanism of two different insulin amyloids is attributed to the difference in the intermolecular interactions and could be correlated with the cytotoxicity. |
format | Online Article Text |
id | pubmed-9123177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91231772022-05-22 Differences in interaction lead to the formation of different types of insulin amyloid Mori, Wakako Kawakami, Ryosuke Niko, Yosuke Haruta, Tomohiro Imamura, Takeshi Shiraki, Kentaro Zako, Tamotsu Sci Rep Article Insulin balls, localized insulin amyloids formed at the site of repeated insulin injections in patients with diabetes, cause poor glycemic control and cytotoxicity. Our previous study has shown that insulin forms two types of amyloids; toxic amyloid formed from the intact insulin ((i)-amyloid) and less-toxic amyloid formed in the presence of the reducing reagent TCEP ((r)-amyloid), suggesting insulin amyloid polymorphism. However, the differences in the formation mechanism and cytotoxicity expression are still unclear. Herein, we demonstrate that the liquid droplets, which are stabilized by electrostatic interactions, appear only in the process of toxic (i)-amyloid formation, but not in the less-toxic (r)-amyloid formation process. The effect of various additives such as arginine, 1,6-hexanediol, and salts on amyloid formation was also examined to investigate interactions that are important for amyloid formation. Our results indicate that the maturation processes of these two amyloids were significantly different, whereas the nucleation by hydrophobic interactions was similar. These results also suggest the difference in the formation mechanism of two different insulin amyloids is attributed to the difference in the intermolecular interactions and could be correlated with the cytotoxicity. Nature Publishing Group UK 2022-05-20 /pmc/articles/PMC9123177/ /pubmed/35595809 http://dx.doi.org/10.1038/s41598-022-12212-6 Text en © The Author(s) 2022 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 Mori, Wakako Kawakami, Ryosuke Niko, Yosuke Haruta, Tomohiro Imamura, Takeshi Shiraki, Kentaro Zako, Tamotsu Differences in interaction lead to the formation of different types of insulin amyloid |
title | Differences in interaction lead to the formation of different types of insulin amyloid |
title_full | Differences in interaction lead to the formation of different types of insulin amyloid |
title_fullStr | Differences in interaction lead to the formation of different types of insulin amyloid |
title_full_unstemmed | Differences in interaction lead to the formation of different types of insulin amyloid |
title_short | Differences in interaction lead to the formation of different types of insulin amyloid |
title_sort | differences in interaction lead to the formation of different types of insulin amyloid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9123177/ https://www.ncbi.nlm.nih.gov/pubmed/35595809 http://dx.doi.org/10.1038/s41598-022-12212-6 |
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