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Development of a model plataform for the search of leishmanicidal compounds based on the selective inhibition of dihydroorotate dehydrogenase

Grant number: 14/01257-8
Support type:Scholarships in Brazil - Master
Effective date (Start): May 01, 2014
Effective date (End): January 31, 2016
Field of knowledge:Biological Sciences - Biochemistry
Principal Investigator:Maria Cristina Nonato Costa
Grantee:Eder Lorenzato Junior
Home Institution: Faculdade de Ciências Farmacêuticas de Ribeirão Preto (FCFRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil

Abstract

The Leishmaniasis correspond to a group of diseases considered neglected tropical diseases characterized by a lack of investment in the development of new therapies by both the public sector and the private sector. In this context, the academy has played an important role in the search for new strategies for prevention and treatment , in particular, the identification and validation of potential macromolecular targets , beyond the search for new bioactive compound that can act as prototypes for the development of new therapies. Within this context, our laboratory has been working on the characterization and evaluation of dihydroorotate dehydrogenase (DHODH) as a potential therapeutic target for diseases caused by trypanosomes, in particular, Leishmaniasis. With the application of molecular biology, biochemistry, spectroscopy and crystallography, X- rays could characterize the DHODH enzyme Leishmania major ( LmDHODH ) . This enzyme plays a key role in the synthesis of pyrimidine nucleotides , which makes this enzyme an important target in the development of new drug candidates that may play antiproliferative and antiparasitic activities. The structural and functional assessment of LmDHODH and different mutants allowed us to use in vitro and in silico in search of potent and selective ligands against the parasite enzyme . Two molecules, in particular so-called LCPSP3027 LCPVL898 and were identified as inhibitors LmDHOH IC50 of 1.66 ± 0.03 mM and 2.82 ± 0.02 mM , respectively. These ligands showed leishmanicidal activity in vitro cultures of Leishmania (V.) braziliensis promastigote form in (LD50 of 2.1 mM for LCPSP3027 LD50 and 2.8 mM for LCPVL898) , proved not cytotoxic to macrophages and amastigotes studies showed a reduction significant indices of infectivity. With the development of this project we intend to continue their studies , based on the synthesis of the compounds and LCPSP3027 LCPVL898 and its analogs , followed by the evaluation of the inhibitory potential for new molecules and the development of a formulation , and the first pre - clinical trials. This project aims to contribute to the construction of knowledge about the potential of selective inhibition of dihydroorotate dehydrogenase as a therapeutic strategy in the fight against leishmaniasis.

Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
GARCIA REIS, RENATA ALMEIDA; LORENZATO, JR., EDER; SILVA, VALERIA CRISTINA; NONATO, MARIA CRISTINA. Recombinant production, crystallization and crystal structure determination of dihydroorotate dehydrogenase from Leishmania (Viannia) braziliensis. ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS, v. 71, n. 5, SI, p. 547-552, MAY 2015. Web of Science Citations: 2.
Academic Publications
(References retrieved automatically from State of São Paulo Research Institutions)
JUNIOR, Eder Lorenzato. Development of a model plataform for the search of leishmanicidal compounds based on the selective inhibition of dihydroorotate dehydrogenase. 2016. Master's Dissertation - Universidade de São Paulo (USP). Faculdade de Ciências Farmacêuticas de Ribeirão Preto Ribeirão Preto.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.