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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...

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Autores principales: Brännström, Kristoffer, Islam, Tohidul, Sandblad, Linda, Olofsson, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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.
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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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