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Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes

[Image: see text] Confinement within nanoscale spaces can dramatically alter the ensemble of conformations flexible species explore. For example, chaperone complexes take advantage of confinement to fold misfolded proteins, while viral capsids transport genomic materials in tight packings. Here we e...

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Autores principales: Alagbe, Busayo D., Gibb, Bruce C., Ashbaugh, Henry S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279555/
https://www.ncbi.nlm.nih.gov/pubmed/34170690
http://dx.doi.org/10.1021/acs.jpcb.1c03640
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author Alagbe, Busayo D.
Gibb, Bruce C.
Ashbaugh, Henry S.
author_facet Alagbe, Busayo D.
Gibb, Bruce C.
Ashbaugh, Henry S.
author_sort Alagbe, Busayo D.
collection PubMed
description [Image: see text] Confinement within nanoscale spaces can dramatically alter the ensemble of conformations flexible species explore. For example, chaperone complexes take advantage of confinement to fold misfolded proteins, while viral capsids transport genomic materials in tight packings. Here we examine the free energy landscapes of n-alkanes confined within supramolecular dimeric complexes of deep-cavity cavitand octa-acid, which have been experimentally demonstrated to force these chains with increasing length to adopt extended, helical, hairpin, and spinning top conformational motifs, using molecular simulations. Alkanes up to n-docosane in both vacuum and water predominantly exhibit a free energy minimum for elongated conformations with a majority of trans dihedrals. Within harmonically sealed cavitand dimers, however, the free energy landscapes as a function of the end-to-end distance between their terminal methyl units exhibit minima that evolve with the length of the alkane. Distinct free energy basins are observed between the helical and hairpin motifs and between the hairpin and chicane motifs whose relative stability changes with the number of carbons in the bound guest. These changes are reminiscent of two state-like protein folding, although the observed alkane conformations confined are more insensitive to temperature perturbation than proteins are. While the chicane motif within the harmonically sealed dimers has not been observed experimentally, this conformation relaxes to the observed spinning top motif once the harmonic restraints are released for the complexes in aqueous solution, indicating that these motifs are related to one another. We do not observe distinct minima between the confined extended and helical motifs, suggesting these conformers are part of a larger linear motif family whose population of gauche dihedral angles grows in proportion to the number of carbons in the chain to ultimately form a helix that fits the alkane within the complex.
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spelling pubmed-82795552021-07-15 Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes Alagbe, Busayo D. Gibb, Bruce C. Ashbaugh, Henry S. J Phys Chem B [Image: see text] Confinement within nanoscale spaces can dramatically alter the ensemble of conformations flexible species explore. For example, chaperone complexes take advantage of confinement to fold misfolded proteins, while viral capsids transport genomic materials in tight packings. Here we examine the free energy landscapes of n-alkanes confined within supramolecular dimeric complexes of deep-cavity cavitand octa-acid, which have been experimentally demonstrated to force these chains with increasing length to adopt extended, helical, hairpin, and spinning top conformational motifs, using molecular simulations. Alkanes up to n-docosane in both vacuum and water predominantly exhibit a free energy minimum for elongated conformations with a majority of trans dihedrals. Within harmonically sealed cavitand dimers, however, the free energy landscapes as a function of the end-to-end distance between their terminal methyl units exhibit minima that evolve with the length of the alkane. Distinct free energy basins are observed between the helical and hairpin motifs and between the hairpin and chicane motifs whose relative stability changes with the number of carbons in the bound guest. These changes are reminiscent of two state-like protein folding, although the observed alkane conformations confined are more insensitive to temperature perturbation than proteins are. While the chicane motif within the harmonically sealed dimers has not been observed experimentally, this conformation relaxes to the observed spinning top motif once the harmonic restraints are released for the complexes in aqueous solution, indicating that these motifs are related to one another. We do not observe distinct minima between the confined extended and helical motifs, suggesting these conformers are part of a larger linear motif family whose population of gauche dihedral angles grows in proportion to the number of carbons in the chain to ultimately form a helix that fits the alkane within the complex. American Chemical Society 2021-06-25 2021-07-08 /pmc/articles/PMC8279555/ /pubmed/34170690 http://dx.doi.org/10.1021/acs.jpcb.1c03640 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Alagbe, Busayo D.
Gibb, Bruce C.
Ashbaugh, Henry S.
Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes
title Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes
title_full Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes
title_fullStr Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes
title_full_unstemmed Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes
title_short Evolution of the Free Energy Landscapes of n-Alkane Guests Bound within Supramolecular Complexes
title_sort evolution of the free energy landscapes of n-alkane guests bound within supramolecular complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279555/
https://www.ncbi.nlm.nih.gov/pubmed/34170690
http://dx.doi.org/10.1021/acs.jpcb.1c03640
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