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Protein unfolding mechanisms and their effects on folding experiments
In this review, I discuss the various methods researchers use to unfold proteins in the lab in order to understand protein folding both in vitro and in vivo. The four main techniques, chemical-, heat-, pressure- and force-denaturation, produce distinctly different unfolded conformational ensembles....
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000Research
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615768/ https://www.ncbi.nlm.nih.gov/pubmed/29034084 http://dx.doi.org/10.12688/f1000research.12070.1 |
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author | Lapidus, Lisa J |
author_facet | Lapidus, Lisa J |
author_sort | Lapidus, Lisa J |
collection | PubMed |
description | In this review, I discuss the various methods researchers use to unfold proteins in the lab in order to understand protein folding both in vitro and in vivo. The four main techniques, chemical-, heat-, pressure- and force-denaturation, produce distinctly different unfolded conformational ensembles. Recent measurements have revealed different folding kinetics from different unfolding mechanisms. Thus, comparing these distinct unfolded ensembles sheds light on the underlying free energy landscape of folding. |
format | Online Article Text |
id | pubmed-5615768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-56157682017-10-12 Protein unfolding mechanisms and their effects on folding experiments Lapidus, Lisa J F1000Res Review In this review, I discuss the various methods researchers use to unfold proteins in the lab in order to understand protein folding both in vitro and in vivo. The four main techniques, chemical-, heat-, pressure- and force-denaturation, produce distinctly different unfolded conformational ensembles. Recent measurements have revealed different folding kinetics from different unfolding mechanisms. Thus, comparing these distinct unfolded ensembles sheds light on the underlying free energy landscape of folding. F1000Research 2017-09-22 /pmc/articles/PMC5615768/ /pubmed/29034084 http://dx.doi.org/10.12688/f1000research.12070.1 Text en Copyright: © 2017 Lapidus LJ http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Lapidus, Lisa J Protein unfolding mechanisms and their effects on folding experiments |
title | Protein unfolding mechanisms and their effects on folding experiments |
title_full | Protein unfolding mechanisms and their effects on folding experiments |
title_fullStr | Protein unfolding mechanisms and their effects on folding experiments |
title_full_unstemmed | Protein unfolding mechanisms and their effects on folding experiments |
title_short | Protein unfolding mechanisms and their effects on folding experiments |
title_sort | protein unfolding mechanisms and their effects on folding experiments |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615768/ https://www.ncbi.nlm.nih.gov/pubmed/29034084 http://dx.doi.org/10.12688/f1000research.12070.1 |
work_keys_str_mv | AT lapiduslisaj proteinunfoldingmechanismsandtheireffectsonfoldingexperiments |