Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site

ABSTRACT: Alzheimer's disease pathology is characterized by β-amyloid plaques and neurofibrillary tangles. Amyloid precursor protein is processed by β and γ secretase, resulting in the production of β-amyloid peptides with a length ranging from 38 to 43 amino acids. Presenilin 1 (PS1) is the ca...

Full description

Autores:
Soto Ospina, Johnny Alejandro
Bedoya Berrío, Gabriel de Jesús
Sepúlveda Falla, Diego Alonso
Villegas Lanau, Carlos Andrés
Araque Marín, Pedronel
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/41094
Acceso en línea:
https://hdl.handle.net/10495/41094
Palabra clave:
Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-1
Presenilin-1
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053764
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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dc.title.spa.fl_str_mv Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
title Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
spellingShingle Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-1
Presenilin-1
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053764
title_short Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
title_full Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
title_fullStr Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
title_full_unstemmed Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
title_sort Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site
dc.creator.fl_str_mv Soto Ospina, Johnny Alejandro
Bedoya Berrío, Gabriel de Jesús
Sepúlveda Falla, Diego Alonso
Villegas Lanau, Carlos Andrés
Araque Marín, Pedronel
dc.contributor.author.none.fl_str_mv Soto Ospina, Johnny Alejandro
Bedoya Berrío, Gabriel de Jesús
Sepúlveda Falla, Diego Alonso
Villegas Lanau, Carlos Andrés
Araque Marín, Pedronel
dc.contributor.researchgroup.spa.fl_str_mv Genética Molecular (GENMOL)
Grupo de Neurociencias de Antioquia
dc.subject.decs.none.fl_str_mv Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-1
Presenilin-1
topic Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-1
Presenilin-1
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053764
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053764
description ABSTRACT: Alzheimer's disease pathology is characterized by β-amyloid plaques and neurofibrillary tangles. Amyloid precursor protein is processed by β and γ secretase, resulting in the production of β-amyloid peptides with a length ranging from 38 to 43 amino acids. Presenilin 1 (PS1) is the catalytic unit of γ-secretase, and more than 200 PS1 pathogenic mutations have been identified as causative for Alzheimer's disease. A complete monocrystal structure of PS1 has not been determined so far due to the presence of two flexible domains. We have developed a complete structural model of PS1 using a computational approach with structure prediction software. Missing fragments Met1-Glut72 and Ser290-Glu375 were modeled and validated by their energetic and stereochemical characteristics. Then, with the complete structure of PS1, we defined that these fragments do not have a direct effect in the structure of the pore. Next, we used our hypothetical model for the analysis of the functional effects of PS1 mutations Ala246GLu, Leu248Pro, Leu248Arg, Leu250Val, Tyr256Ser, Ala260Val, and Val261Phe, localized in the catalytic pore. For this, we used a quantum mechanics/molecular mechanics (QM/MM) hybrid method, evaluating modifications in the topology, potential surface density, and electrostatic potential map of mutated PS1 proteins. We found that each mutation exerts changes resulting in structural modifications of the active site and in the shape of the pore. We suggest this as a valid approach for functional studies of PS1 in view of the possible impact in substrate processing and for the design of targeted therapeutic strategies
publishDate 2021
dc.date.issued.none.fl_str_mv 2021
dc.date.accessioned.none.fl_str_mv 2024-08-11T19:08:34Z
dc.date.available.none.fl_str_mv 2024-08-11T19:08:34Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Soto-Ospina A, Araque Marín P, Bedoya G, Sepulveda-Falla D, Villegas Lanau A. Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site. Front Mol Biosci. 2021 Jun 2;8:649990. doi: 10.3389/fmolb.2021.649990.
dc.identifier.issn.none.fl_str_mv 2296-889X
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/41094
dc.identifier.doi.none.fl_str_mv 10.3389/fmolb.2021.649990
identifier_str_mv Soto-Ospina A, Araque Marín P, Bedoya G, Sepulveda-Falla D, Villegas Lanau A. Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site. Front Mol Biosci. 2021 Jun 2;8:649990. doi: 10.3389/fmolb.2021.649990.
2296-889X
10.3389/fmolb.2021.649990
url https://hdl.handle.net/10495/41094
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Front. Mol. Biosci.
dc.relation.citationendpage.spa.fl_str_mv 15
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 8
dc.relation.ispartofjournal.spa.fl_str_mv Frontiers in Molecular Biosciences
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dc.format.extent.spa.fl_str_mv 15 páginas
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dc.publisher.spa.fl_str_mv Frontiers Media
dc.publisher.place.spa.fl_str_mv Lausana, Suiza
institution Universidad de Antioquia
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spelling Soto Ospina, Johnny AlejandroBedoya Berrío, Gabriel de JesúsSepúlveda Falla, Diego AlonsoVillegas Lanau, Carlos AndrésAraque Marín, PedronelGenética Molecular (GENMOL)Grupo de Neurociencias de Antioquia2024-08-11T19:08:34Z2024-08-11T19:08:34Z2021Soto-Ospina A, Araque Marín P, Bedoya G, Sepulveda-Falla D, Villegas Lanau A. Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric Site. Front Mol Biosci. 2021 Jun 2;8:649990. doi: 10.3389/fmolb.2021.649990.2296-889Xhttps://hdl.handle.net/10495/4109410.3389/fmolb.2021.649990ABSTRACT: Alzheimer's disease pathology is characterized by β-amyloid plaques and neurofibrillary tangles. Amyloid precursor protein is processed by β and γ secretase, resulting in the production of β-amyloid peptides with a length ranging from 38 to 43 amino acids. Presenilin 1 (PS1) is the catalytic unit of γ-secretase, and more than 200 PS1 pathogenic mutations have been identified as causative for Alzheimer's disease. A complete monocrystal structure of PS1 has not been determined so far due to the presence of two flexible domains. We have developed a complete structural model of PS1 using a computational approach with structure prediction software. Missing fragments Met1-Glut72 and Ser290-Glu375 were modeled and validated by their energetic and stereochemical characteristics. Then, with the complete structure of PS1, we defined that these fragments do not have a direct effect in the structure of the pore. Next, we used our hypothetical model for the analysis of the functional effects of PS1 mutations Ala246GLu, Leu248Pro, Leu248Arg, Leu250Val, Tyr256Ser, Ala260Val, and Val261Phe, localized in the catalytic pore. For this, we used a quantum mechanics/molecular mechanics (QM/MM) hybrid method, evaluating modifications in the topology, potential surface density, and electrostatic potential map of mutated PS1 proteins. We found that each mutation exerts changes resulting in structural modifications of the active site and in the shape of the pore. We suggest this as a valid approach for functional studies of PS1 in view of the possible impact in substrate processing and for the design of targeted therapeutic strategiesColombia. Ministerio de Ciencia, Tecnología e Innovación - MincienciasNational Institute of Neurological Disorders and StrokeNational Institute on AgingUniversidad EIACOL0006723COL001074415 páginasapplication/pdfengFrontiers MediaLausana, Suizahttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Protein Predictive Modeling and Simulation of Mutations of Presenilin-1 Familial Alzheimer's Disease on the Orthosteric SiteArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionEnfermedad de AlzheimerAlzheimer DiseasePresenilina-1Presenilin-1https://id.nlm.nih.gov/mesh/D000544https://id.nlm.nih.gov/mesh/D053764Front. Mol. 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