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A lipid boundary separates APP and secretases and limits amyloid β-peptide generation

Millions of patients suffer from Alzheimer's disease, and intensive efforts to find a cure for this devastating disorder center on the proteases, which release the deadly amyloid β-peptide from its precursor. The cutting procedure is thought to be cholesterol dependent and strategies to lower c...

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Detalles Bibliográficos
Autores principales: Kaether, Christoph, Haass, Christian
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172467/
https://www.ncbi.nlm.nih.gov/pubmed/15583026
http://dx.doi.org/10.1083/jcb.200410090
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author Kaether, Christoph
Haass, Christian
author_facet Kaether, Christoph
Haass, Christian
author_sort Kaether, Christoph
collection PubMed
description Millions of patients suffer from Alzheimer's disease, and intensive efforts to find a cure for this devastating disorder center on the proteases, which release the deadly amyloid β-peptide from its precursor. The cutting procedure is thought to be cholesterol dependent and strategies to lower cholesterol as therapeutic treatment are under intensive investigation. Recent findings suggest that the complete proteolytic machinery required for amyloid β-peptide generation is located within lipid rafts. Data by Dotti and colleagues (Abad-Rodriguez et al., 2004), in this issue, suggest that rafts isolate the cutting machinery away from its deadly substrate. These findings describe a novel mechanism for controlling proteolytic activity by building a lipid boundary between proteases and their substrates.
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spelling pubmed-21724672008-03-05 A lipid boundary separates APP and secretases and limits amyloid β-peptide generation Kaether, Christoph Haass, Christian J Cell Biol Reviews Millions of patients suffer from Alzheimer's disease, and intensive efforts to find a cure for this devastating disorder center on the proteases, which release the deadly amyloid β-peptide from its precursor. The cutting procedure is thought to be cholesterol dependent and strategies to lower cholesterol as therapeutic treatment are under intensive investigation. Recent findings suggest that the complete proteolytic machinery required for amyloid β-peptide generation is located within lipid rafts. Data by Dotti and colleagues (Abad-Rodriguez et al., 2004), in this issue, suggest that rafts isolate the cutting machinery away from its deadly substrate. These findings describe a novel mechanism for controlling proteolytic activity by building a lipid boundary between proteases and their substrates. The Rockefeller University Press 2004-12-06 /pmc/articles/PMC2172467/ /pubmed/15583026 http://dx.doi.org/10.1083/jcb.200410090 Text en Copyright © 2004, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Reviews
Kaether, Christoph
Haass, Christian
A lipid boundary separates APP and secretases and limits amyloid β-peptide generation
title A lipid boundary separates APP and secretases and limits amyloid β-peptide generation
title_full A lipid boundary separates APP and secretases and limits amyloid β-peptide generation
title_fullStr A lipid boundary separates APP and secretases and limits amyloid β-peptide generation
title_full_unstemmed A lipid boundary separates APP and secretases and limits amyloid β-peptide generation
title_short A lipid boundary separates APP and secretases and limits amyloid β-peptide generation
title_sort lipid boundary separates app and secretases and limits amyloid β-peptide generation
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172467/
https://www.ncbi.nlm.nih.gov/pubmed/15583026
http://dx.doi.org/10.1083/jcb.200410090
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