Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic

The initial steps of the folding pathway of the C-terminal domain of the murine prion protein <i>m</i>PrP(90–231) are predicted based on the sequential collapse model (SCM). A non-local dominant contact is found to form between the connecting region between helix 1 and β-sheet 1 and the...

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Main Authors: Fernando Bergasa-Caceres, Herschel A. Rabitz
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/16/8619
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spelling doaj-e557abe9a6a742db96b8ab4f92a41c052021-08-26T13:52:05ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-08-01228619861910.3390/ijms22168619Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or PathogenicFernando Bergasa-Caceres0Herschel A. Rabitz1Department of Chemistry, Princeton University, Princeton, NJ 08544, USADepartment of Chemistry, Princeton University, Princeton, NJ 08544, USAThe initial steps of the folding pathway of the C-terminal domain of the murine prion protein <i>m</i>PrP(90–231) are predicted based on the sequential collapse model (SCM). A non-local dominant contact is found to form between the connecting region between helix 1 and β-sheet 1 and the C-terminal region of helix 3. This non-local contact nucleates the most populated molten globule-like intermediate along the folding pathway. A less stable early non-local contact between segments 120–124 and 179–183, located in the middle of helix 2, promotes the formation of a less populated molten globule-like intermediate. The formation of the dominant non-local contact constitutes an example of the postulated Nature’s Shortcut to the prion protein collapse into the native structure. The possible role of the less populated molten globule-like intermediate is explored as the potential initiation point for the folding for three pathogenic mutants (T182A, I214V, and Q211P in mouse prion numbering) of the prion protein.https://www.mdpi.com/1422-0067/22/16/8619prionfoldingpathwayintermediatemolten globuleneuropathology
collection DOAJ
language English
format Article
sources DOAJ
author Fernando Bergasa-Caceres
Herschel A. Rabitz
spellingShingle Fernando Bergasa-Caceres
Herschel A. Rabitz
Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic
International Journal of Molecular Sciences
prion
folding
pathway
intermediate
molten globule
neuropathology
author_facet Fernando Bergasa-Caceres
Herschel A. Rabitz
author_sort Fernando Bergasa-Caceres
title Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic
title_short Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic
title_full Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic
title_fullStr Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic
title_full_unstemmed Identification of Two Early Folding Stage Prion Non-Local Contacts Suggested to Serve as Key Steps in Directing the Final Fold to Be Either Native or Pathogenic
title_sort identification of two early folding stage prion non-local contacts suggested to serve as key steps in directing the final fold to be either native or pathogenic
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-08-01
description The initial steps of the folding pathway of the C-terminal domain of the murine prion protein <i>m</i>PrP(90–231) are predicted based on the sequential collapse model (SCM). A non-local dominant contact is found to form between the connecting region between helix 1 and β-sheet 1 and the C-terminal region of helix 3. This non-local contact nucleates the most populated molten globule-like intermediate along the folding pathway. A less stable early non-local contact between segments 120–124 and 179–183, located in the middle of helix 2, promotes the formation of a less populated molten globule-like intermediate. The formation of the dominant non-local contact constitutes an example of the postulated Nature’s Shortcut to the prion protein collapse into the native structure. The possible role of the less populated molten globule-like intermediate is explored as the potential initiation point for the folding for three pathogenic mutants (T182A, I214V, and Q211P in mouse prion numbering) of the prion protein.
topic prion
folding
pathway
intermediate
molten globule
neuropathology
url https://www.mdpi.com/1422-0067/22/16/8619
work_keys_str_mv AT fernandobergasacaceres identificationoftwoearlyfoldingstageprionnonlocalcontactssuggestedtoserveaskeystepsindirectingthefinalfoldtobeeithernativeorpathogenic
AT herschelarabitz identificationoftwoearlyfoldingstageprionnonlocalcontactssuggestedtoserveaskeystepsindirectingthefinalfoldtobeeithernativeorpathogenic
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