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NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations
Alzheimer’s disease (AD) is classified as an amyloid-related disease. Amyloid beta (Aβ) is a transmembrane protein known to play a major role in the pathogenesis of AD. These Aβ proteins can form ion channels or pores in the cell membrane. Studies have elucidated the structure of the transmembrane d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620595/ https://www.ncbi.nlm.nih.gov/pubmed/34832029 http://dx.doi.org/10.3390/membranes11110799 |
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author | Kim, Minseon Son, Jinyoung Kim, Yongae |
author_facet | Kim, Minseon Son, Jinyoung Kim, Yongae |
author_sort | Kim, Minseon |
collection | PubMed |
description | Alzheimer’s disease (AD) is classified as an amyloid-related disease. Amyloid beta (Aβ) is a transmembrane protein known to play a major role in the pathogenesis of AD. These Aβ proteins can form ion channels or pores in the cell membrane. Studies have elucidated the structure of the transmembrane domain of Aβ ion channels. In addition, various studies have investigated substances that block or inhibit the formation of Aβ ion channels. Zinc ions are considered as potential inhibitors of AD. In this study, we focused on the transmembrane domain and some external domains of the Aβ protein (hAPP-TM), and solution-state NMR was used to confirm the effect on residues of the protein in the presence of zinc ions. In addition, we sought to confirm the structure and orientation of the protein in the presence of the bicelle using solid-state NMR. |
format | Online Article Text |
id | pubmed-8620595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86205952021-11-27 NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations Kim, Minseon Son, Jinyoung Kim, Yongae Membranes (Basel) Article Alzheimer’s disease (AD) is classified as an amyloid-related disease. Amyloid beta (Aβ) is a transmembrane protein known to play a major role in the pathogenesis of AD. These Aβ proteins can form ion channels or pores in the cell membrane. Studies have elucidated the structure of the transmembrane domain of Aβ ion channels. In addition, various studies have investigated substances that block or inhibit the formation of Aβ ion channels. Zinc ions are considered as potential inhibitors of AD. In this study, we focused on the transmembrane domain and some external domains of the Aβ protein (hAPP-TM), and solution-state NMR was used to confirm the effect on residues of the protein in the presence of zinc ions. In addition, we sought to confirm the structure and orientation of the protein in the presence of the bicelle using solid-state NMR. MDPI 2021-10-20 /pmc/articles/PMC8620595/ /pubmed/34832029 http://dx.doi.org/10.3390/membranes11110799 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Minseon Son, Jinyoung Kim, Yongae NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations |
title | NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations |
title_full | NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations |
title_fullStr | NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations |
title_full_unstemmed | NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations |
title_short | NMR Studies of the Ion Channel-Forming Human Amyloid-β with Zinc Ion Concentrations |
title_sort | nmr studies of the ion channel-forming human amyloid-β with zinc ion concentrations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620595/ https://www.ncbi.nlm.nih.gov/pubmed/34832029 http://dx.doi.org/10.3390/membranes11110799 |
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