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The Protein Unfolded State: One, No One and One Hundred Thousand

[Image: see text] Many in vitro studies, in which proteins have been unfolded by the action of a variety of physical or chemical agents, have led to the definition of a folded versus an unfolded state and to the question of what is the nature of the unfolded state. The unstructured nature of this st...

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Autores principales: Pastore, Annalisa, Temussi, Piero Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756289/
https://www.ncbi.nlm.nih.gov/pubmed/36450361
http://dx.doi.org/10.1021/jacs.2c07696
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author Pastore, Annalisa
Temussi, Piero Andrea
author_facet Pastore, Annalisa
Temussi, Piero Andrea
author_sort Pastore, Annalisa
collection PubMed
description [Image: see text] Many in vitro studies, in which proteins have been unfolded by the action of a variety of physical or chemical agents, have led to the definition of a folded versus an unfolded state and to the question of what is the nature of the unfolded state. The unstructured nature of this state could suggest that “the” unfolded state is a unique entity which holds true for all kinds of unfolding processes. This assumption has to be questioned because the unfolding processes under different stress conditions are dictated by entirely different mechanisms. As a consequence, it can be easily understood that the final state, generically referred to as “the unfolded state”, can be completely different for each of the unfolding processes. The present review examines recent data on the characteristics of the unfolded states emerging from experiments under different conditions, focusing specific attention to the level of compaction of the unfolded species.
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spelling pubmed-97562892022-12-17 The Protein Unfolded State: One, No One and One Hundred Thousand Pastore, Annalisa Temussi, Piero Andrea J Am Chem Soc [Image: see text] Many in vitro studies, in which proteins have been unfolded by the action of a variety of physical or chemical agents, have led to the definition of a folded versus an unfolded state and to the question of what is the nature of the unfolded state. The unstructured nature of this state could suggest that “the” unfolded state is a unique entity which holds true for all kinds of unfolding processes. This assumption has to be questioned because the unfolding processes under different stress conditions are dictated by entirely different mechanisms. As a consequence, it can be easily understood that the final state, generically referred to as “the unfolded state”, can be completely different for each of the unfolding processes. The present review examines recent data on the characteristics of the unfolded states emerging from experiments under different conditions, focusing specific attention to the level of compaction of the unfolded species. American Chemical Society 2022-11-30 2022-12-14 /pmc/articles/PMC9756289/ /pubmed/36450361 http://dx.doi.org/10.1021/jacs.2c07696 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Pastore, Annalisa
Temussi, Piero Andrea
The Protein Unfolded State: One, No One and One Hundred Thousand
title The Protein Unfolded State: One, No One and One Hundred Thousand
title_full The Protein Unfolded State: One, No One and One Hundred Thousand
title_fullStr The Protein Unfolded State: One, No One and One Hundred Thousand
title_full_unstemmed The Protein Unfolded State: One, No One and One Hundred Thousand
title_short The Protein Unfolded State: One, No One and One Hundred Thousand
title_sort protein unfolded state: one, no one and one hundred thousand
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756289/
https://www.ncbi.nlm.nih.gov/pubmed/36450361
http://dx.doi.org/10.1021/jacs.2c07696
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