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Membrane translocation of folded proteins

An ever-increasing number of proteins have been shown to translocate across various membranes of bacterial as well as eukaryotic cells in their folded states as a part of physiological and/or pathophysiological processes. Herein, we provide an overview of the systems/processes that are established o...

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Detalles Bibliográficos
Autores principales: Pei, Dehua, Dalbey, Ross E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251779/
https://www.ncbi.nlm.nih.gov/pubmed/35671825
http://dx.doi.org/10.1016/j.jbc.2022.102107
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author Pei, Dehua
Dalbey, Ross E.
author_facet Pei, Dehua
Dalbey, Ross E.
author_sort Pei, Dehua
collection PubMed
description An ever-increasing number of proteins have been shown to translocate across various membranes of bacterial as well as eukaryotic cells in their folded states as a part of physiological and/or pathophysiological processes. Herein, we provide an overview of the systems/processes that are established or likely to involve the membrane translocation of folded proteins, such as protein export by the twin-arginine translocation system in bacteria and chloroplasts, unconventional protein secretion and protein import into the peroxisome in eukaryotes, and the cytosolic entry of proteins (e.g., bacterial toxins) and viruses into eukaryotes. We also discuss the various mechanistic models that have previously been proposed for the membrane translocation of folded proteins including pore/channel formation, local membrane disruption, membrane thinning, and transport by membrane vesicles. Finally, we introduce a newly discovered vesicular transport mechanism, vesicle budding and collapse, and present evidence that vesicle budding and collapse may represent a unifying mechanism that drives some (and potentially all) of folded protein translocation processes.
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spelling pubmed-92517792022-07-06 Membrane translocation of folded proteins Pei, Dehua Dalbey, Ross E. J Biol Chem JBC Reviews An ever-increasing number of proteins have been shown to translocate across various membranes of bacterial as well as eukaryotic cells in their folded states as a part of physiological and/or pathophysiological processes. Herein, we provide an overview of the systems/processes that are established or likely to involve the membrane translocation of folded proteins, such as protein export by the twin-arginine translocation system in bacteria and chloroplasts, unconventional protein secretion and protein import into the peroxisome in eukaryotes, and the cytosolic entry of proteins (e.g., bacterial toxins) and viruses into eukaryotes. We also discuss the various mechanistic models that have previously been proposed for the membrane translocation of folded proteins including pore/channel formation, local membrane disruption, membrane thinning, and transport by membrane vesicles. Finally, we introduce a newly discovered vesicular transport mechanism, vesicle budding and collapse, and present evidence that vesicle budding and collapse may represent a unifying mechanism that drives some (and potentially all) of folded protein translocation processes. American Society for Biochemistry and Molecular Biology 2022-06-04 /pmc/articles/PMC9251779/ /pubmed/35671825 http://dx.doi.org/10.1016/j.jbc.2022.102107 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle JBC Reviews
Pei, Dehua
Dalbey, Ross E.
Membrane translocation of folded proteins
title Membrane translocation of folded proteins
title_full Membrane translocation of folded proteins
title_fullStr Membrane translocation of folded proteins
title_full_unstemmed Membrane translocation of folded proteins
title_short Membrane translocation of folded proteins
title_sort membrane translocation of folded proteins
topic JBC Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251779/
https://www.ncbi.nlm.nih.gov/pubmed/35671825
http://dx.doi.org/10.1016/j.jbc.2022.102107
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