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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...

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Autores principales: Kim, Minseon, Son, Jinyoung, Kim, Yongae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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