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Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein

The development of small-molecule pharmacological chaperones as therapeutics for protein misfolding diseases has proven challenging, partly because their mechanism of action remains unclear. Here we study Fe-TMPyP, a tetrapyrrole that binds to the prion protein PrP and inhibits misfolding, examining...

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Detalles Bibliográficos
Autores principales: Gupta, Amar Nath, Neupane, Krishna, Rezajooei, Negar, Cortez, Leonardo M., Sim, Valerie L., Woodside, Michael T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931252/
https://www.ncbi.nlm.nih.gov/pubmed/27346148
http://dx.doi.org/10.1038/ncomms12058
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author Gupta, Amar Nath
Neupane, Krishna
Rezajooei, Negar
Cortez, Leonardo M.
Sim, Valerie L.
Woodside, Michael T.
author_facet Gupta, Amar Nath
Neupane, Krishna
Rezajooei, Negar
Cortez, Leonardo M.
Sim, Valerie L.
Woodside, Michael T.
author_sort Gupta, Amar Nath
collection PubMed
description The development of small-molecule pharmacological chaperones as therapeutics for protein misfolding diseases has proven challenging, partly because their mechanism of action remains unclear. Here we study Fe-TMPyP, a tetrapyrrole that binds to the prion protein PrP and inhibits misfolding, examining its effects on PrP folding at the single-molecule level with force spectroscopy. Single PrP molecules are unfolded with and without Fe-TMPyP present using optical tweezers. Ligand binding to the native structure increases the unfolding force significantly and alters the transition state for unfolding, making it more brittle and raising the barrier height. Fe-TMPyP also binds the unfolded state, delaying native refolding. Furthermore, Fe-TMPyP binding blocks the formation of a stable misfolded dimer by interfering with intermolecular interactions, acting in a similar manner to some molecular chaperones. The ligand thus promotes native folding by stabilizing the native state while also suppressing interactions driving aggregation.
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spelling pubmed-49312522016-07-12 Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein Gupta, Amar Nath Neupane, Krishna Rezajooei, Negar Cortez, Leonardo M. Sim, Valerie L. Woodside, Michael T. Nat Commun Article The development of small-molecule pharmacological chaperones as therapeutics for protein misfolding diseases has proven challenging, partly because their mechanism of action remains unclear. Here we study Fe-TMPyP, a tetrapyrrole that binds to the prion protein PrP and inhibits misfolding, examining its effects on PrP folding at the single-molecule level with force spectroscopy. Single PrP molecules are unfolded with and without Fe-TMPyP present using optical tweezers. Ligand binding to the native structure increases the unfolding force significantly and alters the transition state for unfolding, making it more brittle and raising the barrier height. Fe-TMPyP also binds the unfolded state, delaying native refolding. Furthermore, Fe-TMPyP binding blocks the formation of a stable misfolded dimer by interfering with intermolecular interactions, acting in a similar manner to some molecular chaperones. The ligand thus promotes native folding by stabilizing the native state while also suppressing interactions driving aggregation. Nature Publishing Group 2016-06-27 /pmc/articles/PMC4931252/ /pubmed/27346148 http://dx.doi.org/10.1038/ncomms12058 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gupta, Amar Nath
Neupane, Krishna
Rezajooei, Negar
Cortez, Leonardo M.
Sim, Valerie L.
Woodside, Michael T.
Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
title Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
title_full Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
title_fullStr Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
title_full_unstemmed Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
title_short Pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
title_sort pharmacological chaperone reshapes the energy landscape for folding and aggregation of the prion protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931252/
https://www.ncbi.nlm.nih.gov/pubmed/27346148
http://dx.doi.org/10.1038/ncomms12058
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