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Concentration-dependent polymorphism of insulin amyloid fibrils
Protein aggregation into highly structured fibrils has long been associated with several neurodegenerative disorders, such as Alzheimer’s or Parkinson’s disease. Polymorphism of amyloid fibrils increases the complexity of disease mechanisms and may be one of the reasons for the slow progress in drug...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910113/ https://www.ncbi.nlm.nih.gov/pubmed/31844588 http://dx.doi.org/10.7717/peerj.8208 |
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author | Sakalauskas, Andrius Ziaunys, Mantas Smirnovas, Vytautas |
author_facet | Sakalauskas, Andrius Ziaunys, Mantas Smirnovas, Vytautas |
author_sort | Sakalauskas, Andrius |
collection | PubMed |
description | Protein aggregation into highly structured fibrils has long been associated with several neurodegenerative disorders, such as Alzheimer’s or Parkinson’s disease. Polymorphism of amyloid fibrils increases the complexity of disease mechanisms and may be one of the reasons for the slow progress in drug research. Here we report protein concentration as another factor leading to polymorphism of insulin amyloid fibrils. Moreover, our data suggests that insulin amyloid conformation can self-replicate only via elongation, while seed-induced nucleation will lead to environment-defined conformation of fibrils. As similar observations were already described for a couple of other amyloid proteins, we suggest it to be a generic mechanism for self-replication of different amyloid fibril conformations. |
format | Online Article Text |
id | pubmed-6910113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69101132019-12-16 Concentration-dependent polymorphism of insulin amyloid fibrils Sakalauskas, Andrius Ziaunys, Mantas Smirnovas, Vytautas PeerJ Biochemistry Protein aggregation into highly structured fibrils has long been associated with several neurodegenerative disorders, such as Alzheimer’s or Parkinson’s disease. Polymorphism of amyloid fibrils increases the complexity of disease mechanisms and may be one of the reasons for the slow progress in drug research. Here we report protein concentration as another factor leading to polymorphism of insulin amyloid fibrils. Moreover, our data suggests that insulin amyloid conformation can self-replicate only via elongation, while seed-induced nucleation will lead to environment-defined conformation of fibrils. As similar observations were already described for a couple of other amyloid proteins, we suggest it to be a generic mechanism for self-replication of different amyloid fibril conformations. PeerJ Inc. 2019-12-10 /pmc/articles/PMC6910113/ /pubmed/31844588 http://dx.doi.org/10.7717/peerj.8208 Text en ©2019 Sakalauskas et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Biochemistry Sakalauskas, Andrius Ziaunys, Mantas Smirnovas, Vytautas Concentration-dependent polymorphism of insulin amyloid fibrils |
title | Concentration-dependent polymorphism of insulin amyloid fibrils |
title_full | Concentration-dependent polymorphism of insulin amyloid fibrils |
title_fullStr | Concentration-dependent polymorphism of insulin amyloid fibrils |
title_full_unstemmed | Concentration-dependent polymorphism of insulin amyloid fibrils |
title_short | Concentration-dependent polymorphism of insulin amyloid fibrils |
title_sort | concentration-dependent polymorphism of insulin amyloid fibrils |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910113/ https://www.ncbi.nlm.nih.gov/pubmed/31844588 http://dx.doi.org/10.7717/peerj.8208 |
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