Busca avançada
Ano de início
Entree


Inhibition of 3-Hydroxykynurenine Transaminase from Aedes aegypti and Anopheles gambiae: A Mosquito-Specific Target to Combat the Transmission of Arboviruses

Texto completo
Autor(es):
Maciel, Larissa G. ; Ferraz, Matheus V. F. ; Oliveira, Andrew A. ; Lins, Roberto D. ; dos Anjos, Janaina V. ; Guido, Rafael V. C. ; Soares, Thereza A.
Número total de Autores: 7
Tipo de documento: Artigo Científico
Fonte: ACS BIO & MED CHEM AU; v. 3, n. 2, p. 12-pg., 2023-02-16.
Resumo

Arboviral infections such as Zika, chikungunya, dengue, and yellow fever pose significant health problems globally. The population at risk is expanding with the geographical distribution of the main transmission vector of these viruses, the Aedes aegypti mosquito. The global spreading of this mosquito is driven by human migration, urbanization, climate change, and the ecological plasticity of the species. Currently, there are no specific treatments for Aedes-borne infections. One strategy to combat different mosquito-borne arboviruses is to design molecules that can specifically inhibit a critical host protein. We obtained the crystal structure of 3-hydroxykynurenine transaminase (AeHKT) from A. aegypti, an essential detoxification enzyme of the tryptophan metabolism pathway. Since AeHKT is found exclusively in mosquitoes, it provides the ideal molecular target for the development of inhibitors. Therefore, we determined and compared the free binding energy of the inhibitors 4-(2-aminophenyl)-4-oxobutyric acid (4OB) and sodium 4-(3-phenyl-1,2,4-oxadiazol-5-yl)butanoate (OXA) to AeHKT and AgHKT from Anopheles gambiae, the only crystal structure of this enzyme previously known. The cocrystallized inhibitor 4OB binds to AgHKT with Ki of 300 mu M. We showed that OXA binds to both AeHKT and AgHKT enzymes with binding energies 2-fold more favorable than the crystallographic inhibitor 4OB and displayed a 2-fold greater residence time t upon binding to AeHKT than 4OB. These findings indicate that the 1,2,4-oxadiazole derivatives are inhibitors of the HKT enzyme not only from A. aegypti but also from A. gambiae. (AU)

Processo FAPESP: 20/12904-5 - Descoberta de inibidores de Plasmodium falciparum a partir de plantas do Cerrado como candidatos a compostos líderes para a malária: estudos integrados de cromatografia de ultra eficiência, espectroscopia e ensaios biológicos
Beneficiário:Rafael Victorio Carvalho Guido
Modalidade de apoio: Auxílio à Pesquisa - Programa BIOTA - Regular
Processo FAPESP: 21/04283-3 - Uma abordagem de múltipla resolução para o polimorfismo de agregados lipopolissacarídicos induzido por metais
Beneficiário:Thereza Amélia Soares da Silva
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 15/07005-3 - Estudos de Biologia Estrutural e Química Medicinal para a descoberta e planejamento de novos agroquímicos
Beneficiário:Andrew Albert de Oliveira
Modalidade de apoio: Bolsas no Brasil - Doutorado Direto
Processo FAPESP: 13/07600-3 - CIBFar - Centro de Inovação em Biodiversidade e Fármacos
Beneficiário:Glaucius Oliva
Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs