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Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99
The 99-residue C-terminal domain of amyloid precursor protein (APP-C99), precursor to amyloid beta (Aβ), is a transmembrane (TM) protein containing intrinsically disordered N- and C-terminal extramembrane domains. Using molecular dynamics (MD) simulations, we show that the structural ensemble of the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907117/ https://www.ncbi.nlm.nih.gov/pubmed/36538482 http://dx.doi.org/10.1073/pnas.2212207119 |
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author | Pantelopulos, George A. Matsuoka, Daisuke Hutchison, James M. Sanders, Charles R. Sugita, Yuji Straub, John E. Thirumalai, D. |
author_facet | Pantelopulos, George A. Matsuoka, Daisuke Hutchison, James M. Sanders, Charles R. Sugita, Yuji Straub, John E. Thirumalai, D. |
author_sort | Pantelopulos, George A. |
collection | PubMed |
description | The 99-residue C-terminal domain of amyloid precursor protein (APP-C99), precursor to amyloid beta (Aβ), is a transmembrane (TM) protein containing intrinsically disordered N- and C-terminal extramembrane domains. Using molecular dynamics (MD) simulations, we show that the structural ensemble of the C99 monomer is best described in terms of thousands of states. The C99 monomer has a propensity to form β-strand in the C-terminal extramembrane domain, which explains the slow spin relaxation times observed in paramagnetic probe NMR experiments. Surprisingly, homodimerization of C99 not only narrows the conformational ensemble from thousands to a few states through the formation of metastable β-strands in extramembrane domains but also stabilizes extramembrane α-helices. The extramembrane domain structure is observed to dramatically impact the homodimerization motif, resulting in the modification of TM domain conformations. Our study provides an atomic-level structural basis for communication between the extramembrane domains of the C99 protein and TM homodimer formation. This finding could serve as a general model for understanding the influence of disordered extramembrane domains on TM protein structure. |
format | Online Article Text |
id | pubmed-9907117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-99071172023-06-20 Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 Pantelopulos, George A. Matsuoka, Daisuke Hutchison, James M. Sanders, Charles R. Sugita, Yuji Straub, John E. Thirumalai, D. Proc Natl Acad Sci U S A Physical Sciences The 99-residue C-terminal domain of amyloid precursor protein (APP-C99), precursor to amyloid beta (Aβ), is a transmembrane (TM) protein containing intrinsically disordered N- and C-terminal extramembrane domains. Using molecular dynamics (MD) simulations, we show that the structural ensemble of the C99 monomer is best described in terms of thousands of states. The C99 monomer has a propensity to form β-strand in the C-terminal extramembrane domain, which explains the slow spin relaxation times observed in paramagnetic probe NMR experiments. Surprisingly, homodimerization of C99 not only narrows the conformational ensemble from thousands to a few states through the formation of metastable β-strands in extramembrane domains but also stabilizes extramembrane α-helices. The extramembrane domain structure is observed to dramatically impact the homodimerization motif, resulting in the modification of TM domain conformations. Our study provides an atomic-level structural basis for communication between the extramembrane domains of the C99 protein and TM homodimer formation. This finding could serve as a general model for understanding the influence of disordered extramembrane domains on TM protein structure. National Academy of Sciences 2022-12-20 2022-12-27 /pmc/articles/PMC9907117/ /pubmed/36538482 http://dx.doi.org/10.1073/pnas.2212207119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Physical Sciences Pantelopulos, George A. Matsuoka, Daisuke Hutchison, James M. Sanders, Charles R. Sugita, Yuji Straub, John E. Thirumalai, D. Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 |
title | Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 |
title_full | Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 |
title_fullStr | Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 |
title_full_unstemmed | Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 |
title_short | Formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein C99 |
title_sort | formation of extramembrane β-strands controls dimerization of transmembrane helices in amyloid precursor protein c99 |
topic | Physical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9907117/ https://www.ncbi.nlm.nih.gov/pubmed/36538482 http://dx.doi.org/10.1073/pnas.2212207119 |
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