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The role of histidines in amyloid β fibril assembly
Low pH has a strong stabilising effect on the fibrillar assembly of amyloid β, which is associated with Alzheimer's disease. The stabilising effect is already pronounced at pH 6.0, suggesting that protonation of histidines might mediate this effect. Through the systematic substitution of the th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434815/ https://www.ncbi.nlm.nih.gov/pubmed/28267202 http://dx.doi.org/10.1002/1873-3468.12616 |
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author | Brännström, Kristoffer Islam, Tohidul Sandblad, Linda Olofsson, Anders |
author_facet | Brännström, Kristoffer Islam, Tohidul Sandblad, Linda Olofsson, Anders |
author_sort | Brännström, Kristoffer |
collection | PubMed |
description | Low pH has a strong stabilising effect on the fibrillar assembly of amyloid β, which is associated with Alzheimer's disease. The stabilising effect is already pronounced at pH 6.0, suggesting that protonation of histidines might mediate this effect. Through the systematic substitution of the three native histidines in Aβ for alanines, we have evaluated their role in fibril stability. Using surface plasmon resonance, we show that at neutral pH the fibrillar forms of all His‐Ala variants are destabilised by a factor of 4–12 compared to wild‐type Aβ. However, none of the His‐Ala Aβ variants impair the stabilising effect of the fibril at low pH. |
format | Online Article Text |
id | pubmed-5434815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54348152017-06-01 The role of histidines in amyloid β fibril assembly Brännström, Kristoffer Islam, Tohidul Sandblad, Linda Olofsson, Anders FEBS Lett Research Letters Low pH has a strong stabilising effect on the fibrillar assembly of amyloid β, which is associated with Alzheimer's disease. The stabilising effect is already pronounced at pH 6.0, suggesting that protonation of histidines might mediate this effect. Through the systematic substitution of the three native histidines in Aβ for alanines, we have evaluated their role in fibril stability. Using surface plasmon resonance, we show that at neutral pH the fibrillar forms of all His‐Ala variants are destabilised by a factor of 4–12 compared to wild‐type Aβ. However, none of the His‐Ala Aβ variants impair the stabilising effect of the fibril at low pH. John Wiley and Sons Inc. 2017-04-03 2017-04 /pmc/articles/PMC5434815/ /pubmed/28267202 http://dx.doi.org/10.1002/1873-3468.12616 Text en © 2017 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Letters Brännström, Kristoffer Islam, Tohidul Sandblad, Linda Olofsson, Anders The role of histidines in amyloid β fibril assembly |
title | The role of histidines in amyloid β fibril assembly |
title_full | The role of histidines in amyloid β fibril assembly |
title_fullStr | The role of histidines in amyloid β fibril assembly |
title_full_unstemmed | The role of histidines in amyloid β fibril assembly |
title_short | The role of histidines in amyloid β fibril assembly |
title_sort | role of histidines in amyloid β fibril assembly |
topic | Research Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434815/ https://www.ncbi.nlm.nih.gov/pubmed/28267202 http://dx.doi.org/10.1002/1873-3468.12616 |
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