Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations

ABSTRACT: Alzheimer's disease manifests itself in brain tissue by neuronal death, due to aggregation of β-amyloid, produced by senile plaques, and hyperphosphorylation of the tau protein, which produces neurofibrillary tangles. One of the genetic markers of the disease is the gene that translat...

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Autores:
Soto Ospina, Johnny Alejandro
Bedoya Berrío, Gabriel de Jesús
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:10495/41092
Acceso en línea:
https://hdl.handle.net/10495/41092
Palabra clave:
Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-2
Presenilin-2
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053766
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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dc.title.spa.fl_str_mv Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
title Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
spellingShingle Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-2
Presenilin-2
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053766
title_short Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
title_full Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
title_fullStr Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
title_full_unstemmed Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
title_sort Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations
dc.creator.fl_str_mv Soto Ospina, Johnny Alejandro
Bedoya Berrío, Gabriel de Jesús
Villegas Lanau, Carlos Andrés
Araque Marín, Pedronel
dc.contributor.author.none.fl_str_mv Soto Ospina, Johnny Alejandro
Bedoya Berrío, Gabriel de Jesús
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-2
Presenilin-2
topic Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-2
Presenilin-2
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053766
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D053766
description ABSTRACT: Alzheimer's disease manifests itself in brain tissue by neuronal death, due to aggregation of β-amyloid, produced by senile plaques, and hyperphosphorylation of the tau protein, which produces neurofibrillary tangles. One of the genetic markers of the disease is the gene that translates the presenilin-2 protein, which has mutations that favor the appearance of the disease and has no reported crystallographic structure. In view of this, protein modeling is performed using prediction and structural refinement tools followed by an energetic and stereochemical characterization for its validation. For the simulation, four reported mutations are chosen, which are Met239Ile, Met239Val, Ser130Leu, and Thr122Arg, all associated with various functional responses. From a theoretical analysis, a preliminary bioinformatic study is made to find the phosphorylation patterns in the protein and the hydropathic index according to the polarity and chemical environment. Molecular visualization was carried out with the Chimera 1.14 software, and the theoretical calculation with the hybrid quantum mechanics/molecular mechanics system from the semi-empirical method, with Spartan18 software and an AustinModel1 basis. These relationships allow for studying the system from a structural approach with the determination of small distance changes, potential surfaces, electrostatic maps, and angle changes, which favor the comparison between wild-type and mutant systems. With the results obtained, it is expected to complement experimental data reported in the literature from models that would allow us to understand the effects of the selected mutations.
publishDate 2021
dc.date.issued.none.fl_str_mv 2021
dc.date.accessioned.none.fl_str_mv 2024-08-11T17:37:45Z
dc.date.available.none.fl_str_mv 2024-08-11T17:37:45Z
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 GJ, Villegas Lanau A. Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations. Biochem Res Int. 2021 Nov 29;2021:9542038. doi: 10.1155/2021/9542038.
dc.identifier.issn.none.fl_str_mv 2090-2247
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/41092
dc.identifier.doi.none.fl_str_mv 10.1155/2021/9542038
dc.identifier.eissn.none.fl_str_mv 2090-2255
identifier_str_mv Soto-Ospina A, Araque Marín P, Bedoya GJ, Villegas Lanau A. Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations. Biochem Res Int. 2021 Nov 29;2021:9542038. doi: 10.1155/2021/9542038.
2090-2247
10.1155/2021/9542038
2090-2255
url https://hdl.handle.net/10495/41092
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Biochem. Res. Int.
dc.relation.citationendpage.spa.fl_str_mv 20
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 2021
dc.relation.ispartofjournal.spa.fl_str_mv Biochemistry Research International
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dc.format.extent.spa.fl_str_mv 20 páginas
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dc.publisher.spa.fl_str_mv Hindawi Pub. Corp.
dc.publisher.place.spa.fl_str_mv Nueva York, Estados Unidos
institution Universidad de Antioquia
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spelling Soto Ospina, Johnny AlejandroBedoya Berrío, Gabriel de JesúsVillegas Lanau, Carlos AndrésAraque Marín, PedronelGenética Molecular (GENMOL)Grupo de Neurociencias de Antioquia2024-08-11T17:37:45Z2024-08-11T17:37:45Z2021Soto-Ospina A, Araque Marín P, Bedoya GJ, Villegas Lanau A. Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease Mutations. Biochem Res Int. 2021 Nov 29;2021:9542038. doi: 10.1155/2021/9542038.2090-2247https://hdl.handle.net/10495/4109210.1155/2021/95420382090-2255ABSTRACT: Alzheimer's disease manifests itself in brain tissue by neuronal death, due to aggregation of β-amyloid, produced by senile plaques, and hyperphosphorylation of the tau protein, which produces neurofibrillary tangles. One of the genetic markers of the disease is the gene that translates the presenilin-2 protein, which has mutations that favor the appearance of the disease and has no reported crystallographic structure. In view of this, protein modeling is performed using prediction and structural refinement tools followed by an energetic and stereochemical characterization for its validation. For the simulation, four reported mutations are chosen, which are Met239Ile, Met239Val, Ser130Leu, and Thr122Arg, all associated with various functional responses. From a theoretical analysis, a preliminary bioinformatic study is made to find the phosphorylation patterns in the protein and the hydropathic index according to the polarity and chemical environment. Molecular visualization was carried out with the Chimera 1.14 software, and the theoretical calculation with the hybrid quantum mechanics/molecular mechanics system from the semi-empirical method, with Spartan18 software and an AustinModel1 basis. These relationships allow for studying the system from a structural approach with the determination of small distance changes, potential surfaces, electrostatic maps, and angle changes, which favor the comparison between wild-type and mutant systems. With the results obtained, it is expected to complement experimental data reported in the literature from models that would allow us to understand the effects of the selected mutations.Universidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIColombia. Ministerio de Ciencia, Tecnología e Innovación - MincienciasCOL0006723COL001074420 páginasapplication/pdfengHindawi Pub. Corp.Nueva York, Estados Unidoshttps://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_abf2Structural Predictive Model of Presenilin-2 Protein and Analysis of Structural Effects of Familial Alzheimer's Disease MutationsArtículo 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-2Presenilin-2https://id.nlm.nih.gov/mesh/D000544https://id.nlm.nih.gov/mesh/D053766Biochem. Res. Int.2012021Biochemistry Research InternationalCaracterización clínica y genética de grupos familiares con enfermedad de Alzheimer y trastornos del movimiento con patrones de herencia mendelianaCODI 2017-15829Minciencias 23411Minciencias 111565741597RoR:03bp5hc83RoR:03fd5ne08PublicationORIGINALBedoyaGabriel_2021_Structural_Predictive_Model.pdfBedoyaGabriel_2021_Structural_Predictive_Model.pdfArtículo de investigaciónapplication/pdf8085620https://bibliotecadigital.udea.edu.co/bitstreams/8da05c4d-5fc4-42c7-a3ee-e685e7726d63/download4166a57c933b49be2cd8931cbea3c372MD51trueAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/91f1cb40-a399-4489-9d9a-ac8350b20a44/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/b5e4fc5f-589e-4a31-ad8d-9ac40832060f/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADTEXTBedoyaGabriel_2021_Structural_Predictive_Model.pdf.txtBedoyaGabriel_2021_Structural_Predictive_Model.pdf.txtExtracted texttext/plain101024https://bibliotecadigital.udea.edu.co/bitstreams/00ed0c22-3dcc-49ea-8539-6dff68404b9d/download10a00175b4f60b7d444d73bf62f324b5MD54falseAnonymousREADTHUMBNAILBedoyaGabriel_2021_Structural_Predictive_Model.pdf.jpgBedoyaGabriel_2021_Structural_Predictive_Model.pdf.jpgGenerated Thumbnailimage/jpeg13588https://bibliotecadigital.udea.edu.co/bitstreams/5b12db62-6795-4dbd-8fff-3fa461e63a1d/download153220c153513013c516be81c64d4cbcMD55falseAnonymousREAD10495/41092oai:bibliotecadigital.udea.edu.co:10495/410922025-03-26 21:08:22.311https://creativecommons.org/licenses/by/4.0/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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