Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno

Detalhes bibliográficos
Ano de defesa: 2021
Autor(a) principal: Nagata, Khayth Marronny Rabelo lattes
Orientador(a): Piquini, Paulo Cesar lattes
Banca de defesa: Machado, Karina dos Santos, Almeida, James Moraes de, Mombach, José Carlos Merino, Rocha, João Batista Teixeira da
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Programa de Pós-Graduação em Física
Departamento: Física
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/28765
Resumo: Every year millions of people die around the world due to viral, bacterial and parasitic infections. Malaria is the fifth leading cause of death for infectious diseases in the world, after respiratory infections, HIV / AIDS, diarrheal diseases and tuberculosis, with the number of victims 3 times higher than the number of victims of current armed conflicts. Malaria is also known as impaludism, terçã fever, quartã fever, maleita and others. It is caused by parasites of the genus Plasmodium, family Plasmodidae, filo Apicomplexa, with about 156 species that infect several vertebrates, and five of them can infect humans: P. falciparum, P. malarie, P. Vivax, P. Knowlesi and P. Ovale, and malaria caused by P. falciparum is the most severe form of the disease. The increasing resistance of the parasite to antimalarial chemotherapy has worried the medical community and intensified the search for new antimalarial drugs. The purine nucleoside phosphorylase enzyme (PfPNP) catalyzes the formation of hypoxanthine, essential for the purine synthesis pathway. The enzyme enoyl reductase (PfENR), has significant importance in regulating the fatty acid elongation cycle. Beta Cariophilene and Beta Bisabolene are sesquiterpenes found in various plants such as cinnamon (Cinnamomum spp.), Black pepper (Piper nigrum L.), clove (Syzygium aromaticum), cannabis (Cannabis sativa L.) lavender (Lavandula angustifolia), oregano (Origanum vulgare L.), rosemary (Rosmarinus officinalis) Copaíba (copaífera reticulata), and exhibit anti-inflammatory, anticarcinogenic, antimicrobial, antioxidative and analgesic therapeutic properties. In this work, three-dimensional models for the enzymes were constructed from structures obtained in the Protein Data Bank database using Modeller 9.23 software and Verify3D, MolProbity and ModFold validation techniques were used to determine the stereochemical quality of the models. The Molecular Dynamics (DM) of the enzymes and the topology of the ligands were performed using the GROMACS 5.1.4 software package, with the Gromos 96.1 force field (53A6) Calculations of Root Mean Square Deviation (RMSD), Root Mean Square Fluctuation (RMSF) and radius of gyration (Rg) were used for comparison and analysis of the systems with binders in relation to the free form. The binding sites of the enzymes with the ligands were obtained with Autodock Vina 1.1.2 and Autodock Tools 1.5.6 molecular docking software. Molecular docking simulations were also carried out with Artemisinin, which is the most recently used treatment for malaria, and with triclosan for PfEACPR, as this is a known inhibitor of this enzyme and with inosine, which is a natural inhibitor of the enzyme PfPNP.
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spelling 2023-04-19T18:32:05Z2023-04-19T18:32:05Z2021-08-31http://repositorio.ufsm.br/handle/1/28765Every year millions of people die around the world due to viral, bacterial and parasitic infections. Malaria is the fifth leading cause of death for infectious diseases in the world, after respiratory infections, HIV / AIDS, diarrheal diseases and tuberculosis, with the number of victims 3 times higher than the number of victims of current armed conflicts. Malaria is also known as impaludism, terçã fever, quartã fever, maleita and others. It is caused by parasites of the genus Plasmodium, family Plasmodidae, filo Apicomplexa, with about 156 species that infect several vertebrates, and five of them can infect humans: P. falciparum, P. malarie, P. Vivax, P. Knowlesi and P. Ovale, and malaria caused by P. falciparum is the most severe form of the disease. The increasing resistance of the parasite to antimalarial chemotherapy has worried the medical community and intensified the search for new antimalarial drugs. The purine nucleoside phosphorylase enzyme (PfPNP) catalyzes the formation of hypoxanthine, essential for the purine synthesis pathway. The enzyme enoyl reductase (PfENR), has significant importance in regulating the fatty acid elongation cycle. Beta Cariophilene and Beta Bisabolene are sesquiterpenes found in various plants such as cinnamon (Cinnamomum spp.), Black pepper (Piper nigrum L.), clove (Syzygium aromaticum), cannabis (Cannabis sativa L.) lavender (Lavandula angustifolia), oregano (Origanum vulgare L.), rosemary (Rosmarinus officinalis) Copaíba (copaífera reticulata), and exhibit anti-inflammatory, anticarcinogenic, antimicrobial, antioxidative and analgesic therapeutic properties. In this work, three-dimensional models for the enzymes were constructed from structures obtained in the Protein Data Bank database using Modeller 9.23 software and Verify3D, MolProbity and ModFold validation techniques were used to determine the stereochemical quality of the models. The Molecular Dynamics (DM) of the enzymes and the topology of the ligands were performed using the GROMACS 5.1.4 software package, with the Gromos 96.1 force field (53A6) Calculations of Root Mean Square Deviation (RMSD), Root Mean Square Fluctuation (RMSF) and radius of gyration (Rg) were used for comparison and analysis of the systems with binders in relation to the free form. The binding sites of the enzymes with the ligands were obtained with Autodock Vina 1.1.2 and Autodock Tools 1.5.6 molecular docking software. Molecular docking simulations were also carried out with Artemisinin, which is the most recently used treatment for malaria, and with triclosan for PfEACPR, as this is a known inhibitor of this enzyme and with inosine, which is a natural inhibitor of the enzyme PfPNP.Todos os anos milhões de pessoas morrem ao redor do mundo devido a infecções virais, bacterianas e parasitárias. A malária é a quinta causa de morte por doenças infecciosas no mundo, depois de infecções respiratórias, HIV/AIDS, doenças diarreicas e tuberculose, com o número de vítimas 3 vezes maior que o número de vítimas por conflitos armados da atualidade. A malária é também conhecida como impaludismo, febre terçã, febre quartã, maleita e outros, é causada por parasitas do gênero Plasmodium, família Plasmodidae, filo Apicomplexa, havendo cerca de 156 espécies que infectam vários vertebrados, e cinco delas podem infectar humanos: P. falciparum, P. malarie, P. Vivax, P. Knowlesi e P. Ovale, sendo a malária causada pelo P. falciparum é a forma mais grave da doença. A resistência crescente do parasita em relação a quimioterapia antimalárica tem preocupado a comunidade médica e intensificado a busca por novos medicamentos antimaláricos. As enzimas Purina Nucleosídeo Fosforilase (PfPNP) e Enoil Redutase (Enoyl Acil Carrier Protein Reductase) (PfEACPR) do P. falciparum são potenciais alvos para eliminação do parasita. A primeira catalisa a formação de hipoxantina, essencial para a via de síntese de purinas, enquanto a segunda possui importância significativa na regulação do ciclo de elongamento de ácidos graxos. O Beta Cariofileno e o Beta Bisaboleno são sesquiterpenos encontrados em diversas plantas como canela (Cinnamomum spp.), Pimenta preta (Piper nigrum L.), cravo (Syzygium aromaticum), cannabis (Cannabis sativa L.) lavanda (Lavandula angustifolia), orégano (Origanum vulgare L.), alecrim (Rosmarinus officinalis) Copaíba (copaífera reticulata), e apresentam propriedades terapêuticas anti-inflamatórias , anticarcinógenicas , antimicrobianas , antioxidativas e atividades analgésicas. Neste trabalho, foram construídos modelos tridimensionais para as enzimas a partir de estruturas obtidas no banco de dados Protein Data Bank, utilizando o software Modeller 9.23 e foram utilizadas as técnicas de validação Verify3D, Procheck e ModFold para determinar a qualidade estereoquímica dos modelos. As Dinâmicas Moleculares (DM) das enzimas e a topologia dos ligantes foram realizadas utilizando o pacote de software GROMACS 2020, sob CNTP. Os cálculos de desvio médio quadrático (RMSD), Raiz quadrada da flutuação quadrática média (RMSF) e raio de giro (Rg) foram utilizados para comparação e análise dos sistemas com ligantes em relação a forma livre. Os sítios de ligação das enzimas e a interação com os ligantes foram obtidos com os softwares de docagem molecular Autodock Vina 1.1.2 e Autodock Tools 1.5.6. Foram também realizadas simulações de docking molecular com a Artemisinina, que é o tratamento mais utilizado recentemente para a malária, e com o triclosan para a PfEACPR, pois este é um inibidor conhecido desta enzima e com a inosina, que é um inibidor natural da enzima PfPNP. Os modelos construídos para as enzimas apresentaram boa qualidade estereoquímica e na estrutura 3D de acordo com as técnicas de validação empregadas. A estrutura da enzima PfEACPR apresentou boa estabilidade e compactação, mostradas pelos resultados da Dinâmica Molecular, já para a enzima PfPNP não foi possivel observar estabilidade pois o tempo de simulação para a mesma foi insuficiente. Nos resultados de Docking Molecular pudemos observar que os ligantes Beta bisaboleno interagem em regiões muito próximas entre si e da Artemisinina, através de interações hidrofóbicas nas duas enzimas.porUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em FísicaUFSMBrasilFísicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessPlasmodium falciparumMaláriaEnoil RedutasePurina Nucleosídeo FosforilaseSesquiterpenosMalariaEnoyl ReductasePurine Nucleoside PhosphorylaseSesquiterpenesCNPQ::CIENCIAS EXATAS E DA TERRA::FISICAEstudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofilenoIn silico study of the interaction between the Purine Nucleoside Phosphorylase and Enoy Reductase enzymes of P. falciparum with beta-bisolol and beta-caryophylleneinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisPiquini, Paulo Cesarhttp://lattes.cnpq.br/4496249071363237Machado, Karina dos SantosAlmeida, James Moraes deMombach, José Carlos MerinoRocha, João Batista Teixeira dahttp://lattes.cnpq.br/4397824781057067Nagata, Khayth Marronny Rabelo100500000006600fd6922d3-ec6f-44ef-947e-a60a90ff969116b220e7-ac37-4d72-8b35-2de3ab21958eda1b8d34-fab2-4eef-8d6f-b38d56b4fc81def446a3-0825-4ffd-b7ec-8169b7832567e15ea5f5-7322-4847-9de9-319a0545959219b305d5-beed-4822-a095-c2a70a1006e5reponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALTES_PPGFISICA_2021_NAGATA_KHAYTH.pdfTES_PPGFISICA_2021_NAGATA_KHAYTH.pdfTese de Doutoradoapplication/pdf12427417http://repositorio.ufsm.br/bitstream/1/28765/1/TES_PPGFISICA_2021_NAGATA_KHAYTH.pdfd8e7afeb3b51f541590bc80fe9932828MD51LICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
dc.title.alternative.eng.fl_str_mv In silico study of the interaction between the Purine Nucleoside Phosphorylase and Enoy Reductase enzymes of P. falciparum with beta-bisolol and beta-caryophyllene
title Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
spellingShingle Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
Nagata, Khayth Marronny Rabelo
Plasmodium falciparum
Malária
Enoil Redutase
Purina Nucleosídeo Fosforilase
Sesquiterpenos
Malaria
Enoyl Reductase
Purine Nucleoside Phosphorylase
Sesquiterpenes
CNPQ::CIENCIAS EXATAS E DA TERRA::FISICA
title_short Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
title_full Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
title_fullStr Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
title_full_unstemmed Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
title_sort Estudo in silico da interação entre as enzimas Purina Nucleosídeo Fosforilase e Enoil Redutase do P. falciparum com artemisinina, beta bisaboleno e beta cariofileno
author Nagata, Khayth Marronny Rabelo
author_facet Nagata, Khayth Marronny Rabelo
author_role author
dc.contributor.advisor1.fl_str_mv Piquini, Paulo Cesar
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4496249071363237
dc.contributor.referee1.fl_str_mv Machado, Karina dos Santos
dc.contributor.referee2.fl_str_mv Almeida, James Moraes de
dc.contributor.referee3.fl_str_mv Mombach, José Carlos Merino
dc.contributor.referee4.fl_str_mv Rocha, João Batista Teixeira da
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/4397824781057067
dc.contributor.author.fl_str_mv Nagata, Khayth Marronny Rabelo
contributor_str_mv Piquini, Paulo Cesar
Machado, Karina dos Santos
Almeida, James Moraes de
Mombach, José Carlos Merino
Rocha, João Batista Teixeira da
dc.subject.por.fl_str_mv Plasmodium falciparum
Malária
Enoil Redutase
Purina Nucleosídeo Fosforilase
Sesquiterpenos
topic Plasmodium falciparum
Malária
Enoil Redutase
Purina Nucleosídeo Fosforilase
Sesquiterpenos
Malaria
Enoyl Reductase
Purine Nucleoside Phosphorylase
Sesquiterpenes
CNPQ::CIENCIAS EXATAS E DA TERRA::FISICA
dc.subject.eng.fl_str_mv Malaria
Enoyl Reductase
Purine Nucleoside Phosphorylase
Sesquiterpenes
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::FISICA
description Every year millions of people die around the world due to viral, bacterial and parasitic infections. Malaria is the fifth leading cause of death for infectious diseases in the world, after respiratory infections, HIV / AIDS, diarrheal diseases and tuberculosis, with the number of victims 3 times higher than the number of victims of current armed conflicts. Malaria is also known as impaludism, terçã fever, quartã fever, maleita and others. It is caused by parasites of the genus Plasmodium, family Plasmodidae, filo Apicomplexa, with about 156 species that infect several vertebrates, and five of them can infect humans: P. falciparum, P. malarie, P. Vivax, P. Knowlesi and P. Ovale, and malaria caused by P. falciparum is the most severe form of the disease. The increasing resistance of the parasite to antimalarial chemotherapy has worried the medical community and intensified the search for new antimalarial drugs. The purine nucleoside phosphorylase enzyme (PfPNP) catalyzes the formation of hypoxanthine, essential for the purine synthesis pathway. The enzyme enoyl reductase (PfENR), has significant importance in regulating the fatty acid elongation cycle. Beta Cariophilene and Beta Bisabolene are sesquiterpenes found in various plants such as cinnamon (Cinnamomum spp.), Black pepper (Piper nigrum L.), clove (Syzygium aromaticum), cannabis (Cannabis sativa L.) lavender (Lavandula angustifolia), oregano (Origanum vulgare L.), rosemary (Rosmarinus officinalis) Copaíba (copaífera reticulata), and exhibit anti-inflammatory, anticarcinogenic, antimicrobial, antioxidative and analgesic therapeutic properties. In this work, three-dimensional models for the enzymes were constructed from structures obtained in the Protein Data Bank database using Modeller 9.23 software and Verify3D, MolProbity and ModFold validation techniques were used to determine the stereochemical quality of the models. The Molecular Dynamics (DM) of the enzymes and the topology of the ligands were performed using the GROMACS 5.1.4 software package, with the Gromos 96.1 force field (53A6) Calculations of Root Mean Square Deviation (RMSD), Root Mean Square Fluctuation (RMSF) and radius of gyration (Rg) were used for comparison and analysis of the systems with binders in relation to the free form. The binding sites of the enzymes with the ligands were obtained with Autodock Vina 1.1.2 and Autodock Tools 1.5.6 molecular docking software. Molecular docking simulations were also carried out with Artemisinin, which is the most recently used treatment for malaria, and with triclosan for PfEACPR, as this is a known inhibitor of this enzyme and with inosine, which is a natural inhibitor of the enzyme PfPNP.
publishDate 2021
dc.date.issued.fl_str_mv 2021-08-31
dc.date.accessioned.fl_str_mv 2023-04-19T18:32:05Z
dc.date.available.fl_str_mv 2023-04-19T18:32:05Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/28765
url http://repositorio.ufsm.br/handle/1/28765
dc.language.iso.fl_str_mv por
language por
dc.relation.cnpq.fl_str_mv 100500000006
dc.relation.confidence.fl_str_mv 600
dc.relation.authority.fl_str_mv fd6922d3-ec6f-44ef-947e-a60a90ff9691
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dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Física
dc.publisher.initials.fl_str_mv UFSM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Física
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
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