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...
- 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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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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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 |
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https://hdl.handle.net/10495/41094 |
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eng |
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eng |
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Front. Mol. Biosci. |
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15 |
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1 |
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8 |
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Frontiers in Molecular Biosciences |
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openAccess |
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15 páginas |
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application/pdf |
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Frontiers Media |
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Lausana, Suiza |
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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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