Visualization of Protein Folding Funnels in Lattice Models

Detalhes bibliográficos
Autor(a) principal: Oliveira, Antonio B. [UNESP]
Data de Publicação: 2014
Outros Autores: Fatore, Francisco M., Paulovich, Fernando V., Oliveira, Osvaldo N., Leite, Vitor Barbanti Pereira [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0100861
http://hdl.handle.net/11449/111625
Resumo: Protein folding occurs in a very high dimensional phase space with an exponentially large number of states, and according to the energy landscape theory it exhibits a topology resembling a funnel. In this statistical approach, the folding mechanism is unveiled by describing the local minima in an effective one-dimensional representation. Other approaches based on potential energy landscapes address the hierarchical structure of local energy minima through disconnectivity graphs. In this paper, we introduce a metric to describe the distance between any two conformations, which also allows us to go beyond the one-dimensional representation and visualize the folding funnel in 2D and 3D. In this way it is possible to assess the folding process in detail, e. g., by identifying the connectivity between conformations and establishing the paths to reach the native state, in addition to regions where trapping may occur. Unlike the disconnectivity maps method, which is based on the kinetic connections between states, our methodology is based on structural similarities inferred from the new metric. The method was developed in a 27-mer protein lattice model, folded into a 3x3x3 cube. Five sequences were studied and distinct funnels were generated in an analysis restricted to conformations from the transition-state to the native configuration. Consistent with the expected results from the energy landscape theory, folding routes can be visualized to probe different regions of the phase space, as well as determine the difficulty in folding of the distinct sequences. Changes in the landscape due to mutations were visualized, with the comparison between wild and mutated local minima in a single map, which serves to identify different trapping regions. The extension of this approach to more realistic models and its use in combination with other approaches are discussed.
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spelling Visualization of Protein Folding Funnels in Lattice ModelsProtein folding occurs in a very high dimensional phase space with an exponentially large number of states, and according to the energy landscape theory it exhibits a topology resembling a funnel. In this statistical approach, the folding mechanism is unveiled by describing the local minima in an effective one-dimensional representation. Other approaches based on potential energy landscapes address the hierarchical structure of local energy minima through disconnectivity graphs. In this paper, we introduce a metric to describe the distance between any two conformations, which also allows us to go beyond the one-dimensional representation and visualize the folding funnel in 2D and 3D. In this way it is possible to assess the folding process in detail, e. g., by identifying the connectivity between conformations and establishing the paths to reach the native state, in addition to regions where trapping may occur. Unlike the disconnectivity maps method, which is based on the kinetic connections between states, our methodology is based on structural similarities inferred from the new metric. The method was developed in a 27-mer protein lattice model, folded into a 3x3x3 cube. Five sequences were studied and distinct funnels were generated in an analysis restricted to conformations from the transition-state to the native configuration. Consistent with the expected results from the energy landscape theory, folding routes can be visualized to probe different regions of the phase space, as well as determine the difficulty in folding of the distinct sequences. Changes in the landscape due to mutations were visualized, with the comparison between wild and mutated local minima in a single map, which serves to identify different trapping regions. The extension of this approach to more realistic models and its use in combination with other approaches are discussed.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)nBioNet network (Brazil)Univ Estadual Paulista, Dept Fis, Inst Biociencias Letras & Ciencias Exatas, Sao Paulo, BrazilUniv Sao Paulo, Inst Ciencias Matemat & Comp, Sao Paulo, BrazilUniv Sao Paulo, Inst Fis Sao Carlos, Sao Paulo, BrazilUniv Estadual Paulista, Dept Fis, Inst Biociencias Letras & Ciencias Exatas, Sao Paulo, BrazilPublic Library ScienceUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Oliveira, Antonio B. [UNESP]Fatore, Francisco M.Paulovich, Fernando V.Oliveira, Osvaldo N.Leite, Vitor Barbanti Pereira [UNESP]2014-12-03T13:08:50Z2014-12-03T13:08:50Z2014-07-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article9application/pdfhttp://dx.doi.org/10.1371/journal.pone.0100861Plos One. San Francisco: Public Library Science, v. 9, n. 7, 9 p., 2014.1932-6203http://hdl.handle.net/11449/11162510.1371/journal.pone.0100861WOS:000338763800007WOS000338763800007.pdf0500034174785796Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPLOS ONE2.7661,164info:eu-repo/semantics/openAccess2023-10-21T06:08:27Zoai:repositorio.unesp.br:11449/111625Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:32:00.469951Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Visualization of Protein Folding Funnels in Lattice Models
title Visualization of Protein Folding Funnels in Lattice Models
spellingShingle Visualization of Protein Folding Funnels in Lattice Models
Oliveira, Antonio B. [UNESP]
title_short Visualization of Protein Folding Funnels in Lattice Models
title_full Visualization of Protein Folding Funnels in Lattice Models
title_fullStr Visualization of Protein Folding Funnels in Lattice Models
title_full_unstemmed Visualization of Protein Folding Funnels in Lattice Models
title_sort Visualization of Protein Folding Funnels in Lattice Models
author Oliveira, Antonio B. [UNESP]
author_facet Oliveira, Antonio B. [UNESP]
Fatore, Francisco M.
Paulovich, Fernando V.
Oliveira, Osvaldo N.
Leite, Vitor Barbanti Pereira [UNESP]
author_role author
author2 Fatore, Francisco M.
Paulovich, Fernando V.
Oliveira, Osvaldo N.
Leite, Vitor Barbanti Pereira [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Oliveira, Antonio B. [UNESP]
Fatore, Francisco M.
Paulovich, Fernando V.
Oliveira, Osvaldo N.
Leite, Vitor Barbanti Pereira [UNESP]
description Protein folding occurs in a very high dimensional phase space with an exponentially large number of states, and according to the energy landscape theory it exhibits a topology resembling a funnel. In this statistical approach, the folding mechanism is unveiled by describing the local minima in an effective one-dimensional representation. Other approaches based on potential energy landscapes address the hierarchical structure of local energy minima through disconnectivity graphs. In this paper, we introduce a metric to describe the distance between any two conformations, which also allows us to go beyond the one-dimensional representation and visualize the folding funnel in 2D and 3D. In this way it is possible to assess the folding process in detail, e. g., by identifying the connectivity between conformations and establishing the paths to reach the native state, in addition to regions where trapping may occur. Unlike the disconnectivity maps method, which is based on the kinetic connections between states, our methodology is based on structural similarities inferred from the new metric. The method was developed in a 27-mer protein lattice model, folded into a 3x3x3 cube. Five sequences were studied and distinct funnels were generated in an analysis restricted to conformations from the transition-state to the native configuration. Consistent with the expected results from the energy landscape theory, folding routes can be visualized to probe different regions of the phase space, as well as determine the difficulty in folding of the distinct sequences. Changes in the landscape due to mutations were visualized, with the comparison between wild and mutated local minima in a single map, which serves to identify different trapping regions. The extension of this approach to more realistic models and its use in combination with other approaches are discussed.
publishDate 2014
dc.date.none.fl_str_mv 2014-12-03T13:08:50Z
2014-12-03T13:08:50Z
2014-07-10
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1371/journal.pone.0100861
Plos One. San Francisco: Public Library Science, v. 9, n. 7, 9 p., 2014.
1932-6203
http://hdl.handle.net/11449/111625
10.1371/journal.pone.0100861
WOS:000338763800007
WOS000338763800007.pdf
0500034174785796
url http://dx.doi.org/10.1371/journal.pone.0100861
http://hdl.handle.net/11449/111625
identifier_str_mv Plos One. San Francisco: Public Library Science, v. 9, n. 7, 9 p., 2014.
1932-6203
10.1371/journal.pone.0100861
WOS:000338763800007
WOS000338763800007.pdf
0500034174785796
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv PLOS ONE
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application/pdf
dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
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repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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