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An Outlook on the Complexity of Protein Morphogenesis in Health and Disease
The study of the mechanisms whereby proteins achieve their native functionally competent conformation has been a key issue in molecular biosciences over the last 6 decades. Nevertheless, there are several debated issues and open problems concerning some aspects of this fundamental problem. By consid...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234464/ https://www.ncbi.nlm.nih.gov/pubmed/35769915 http://dx.doi.org/10.3389/fmolb.2022.909567 |
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author | Brunori, Maurizio Gianni, Stefano |
author_facet | Brunori, Maurizio Gianni, Stefano |
author_sort | Brunori, Maurizio |
collection | PubMed |
description | The study of the mechanisms whereby proteins achieve their native functionally competent conformation has been a key issue in molecular biosciences over the last 6 decades. Nevertheless, there are several debated issues and open problems concerning some aspects of this fundamental problem. By considering the emerging complexity of the so-called “native state,” we attempt hereby to propose a personal account on some of the key topics in the field, ranging from the relationships between misfolding and diseases to the significance of protein disorder. Finally, we briefly describe the recent and exciting advances in predicting protein structures from their amino acid sequence. |
format | Online Article Text |
id | pubmed-9234464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92344642022-06-28 An Outlook on the Complexity of Protein Morphogenesis in Health and Disease Brunori, Maurizio Gianni, Stefano Front Mol Biosci Molecular Biosciences The study of the mechanisms whereby proteins achieve their native functionally competent conformation has been a key issue in molecular biosciences over the last 6 decades. Nevertheless, there are several debated issues and open problems concerning some aspects of this fundamental problem. By considering the emerging complexity of the so-called “native state,” we attempt hereby to propose a personal account on some of the key topics in the field, ranging from the relationships between misfolding and diseases to the significance of protein disorder. Finally, we briefly describe the recent and exciting advances in predicting protein structures from their amino acid sequence. Frontiers Media S.A. 2022-06-13 /pmc/articles/PMC9234464/ /pubmed/35769915 http://dx.doi.org/10.3389/fmolb.2022.909567 Text en Copyright © 2022 Brunori and Gianni. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Brunori, Maurizio Gianni, Stefano An Outlook on the Complexity of Protein Morphogenesis in Health and Disease |
title | An Outlook on the Complexity of Protein Morphogenesis in Health and Disease |
title_full | An Outlook on the Complexity of Protein Morphogenesis in Health and Disease |
title_fullStr | An Outlook on the Complexity of Protein Morphogenesis in Health and Disease |
title_full_unstemmed | An Outlook on the Complexity of Protein Morphogenesis in Health and Disease |
title_short | An Outlook on the Complexity of Protein Morphogenesis in Health and Disease |
title_sort | outlook on the complexity of protein morphogenesis in health and disease |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234464/ https://www.ncbi.nlm.nih.gov/pubmed/35769915 http://dx.doi.org/10.3389/fmolb.2022.909567 |
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