Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Pantelopulos, George A., Matsuoka, Daisuke, Hutchison, James M., Sanders, Charles R., Sugita, Yuji, Straub, John E., Thirumalai, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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
_version_ 1784884108044795904
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
work_keys_str_mv AT pantelopulosgeorgea formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99
AT matsuokadaisuke formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99
AT hutchisonjamesm formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99
AT sanderscharlesr formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99
AT sugitayuji formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99
AT straubjohne formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99
AT thirumalaid formationofextramembranebstrandscontrolsdimerizationoftransmembranehelicesinamyloidprecursorproteinc99