Your browser doesn't support javascript.
Yeast-based high-throughput screens for discovery of kinase inhibitors for neglected diseases.
Tavella, T A; Cassiano, G C; Costa, Fabio Trindade Maranhão; Sunnerhagen, P; Bilsland, E.
  • Tavella TA; Laboratory of Tropical Diseases-Prof. Luiz Jacintho da Silva, Department of Genetics, Evolution and Bioagents, University of Campinas, Campinas, SP, Brazil.
  • Cassiano GC; Laboratory of Tropical Diseases-Prof. Luiz Jacintho da Silva, Department of Genetics, Evolution and Bioagents, University of Campinas, Campinas, SP, Brazil; Global Health and Tropical Medicine (GHTM), Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisbon, Portugal.
  • Costa FTM; Laboratory of Tropical Diseases-Prof. Luiz Jacintho da Silva, Department of Genetics, Evolution and Bioagents, University of Campinas, Campinas, SP, Brazil.
  • Sunnerhagen P; Department of Chemistry and Molecular Biology, Lundberg Laboratory, University of Gothenburg, Gothenburg, Sweden.
  • Bilsland E; Laboratory of Tropical Diseases-Prof. Luiz Jacintho da Silva, Department of Genetics, Evolution and Bioagents, University of Campinas, Campinas, SP, Brazil; Department of Structural and Functional Biology, Institute of Biology, UNICAMP, Campinas, Brazil; Synthetic Biology Laboratory, Institute of Bi
Adv Protein Chem Struct Biol ; 124: 275-309, 2021.
Article in English | MEDLINE | ID: covidwho-1375869
ABSTRACT
The discovery and development of a new drug is a complex, time consuming and costly process that typically takes over 10 years and costs around 1 billion dollars from bench to market. This scenario makes the discovery of novel drugs targeting neglected tropical diseases (NTDs), which afflict in particular people in low-income countries, prohibitive. Despite the intensive use of High-Throughput Screening (HTS) in the past decades, the speed with which new drugs come to the market has remained constant, generating doubts about the efficacy of this approach. Here we review a few of the yeast-based high-throughput approaches that can work synergistically with parasite-based, in vitro, or in silico methods to identify and optimize novel antiparasitic compounds. These yeast-based methods range from HTP screens to identify novel hits against promising parasite kinase targets to the identification of potential antiparasitic kinase inhibitors extracted from databases of yeast chemical genetic screens.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Protein Kinases / Saccharomyces cerevisiae / Protein Kinase Inhibitors / Drug Discovery / Neglected Diseases Type of study: Prognostic study Topics: Traditional medicine Limits: Humans Language: English Journal: Adv Protein Chem Struct Biol Journal subject: Biology / Biochemistry Year: 2021 Document Type: Article Affiliation country: Bs.apcsb.2020.09.007

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Protein Kinases / Saccharomyces cerevisiae / Protein Kinase Inhibitors / Drug Discovery / Neglected Diseases Type of study: Prognostic study Topics: Traditional medicine Limits: Humans Language: English Journal: Adv Protein Chem Struct Biol Journal subject: Biology / Biochemistry Year: 2021 Document Type: Article Affiliation country: Bs.apcsb.2020.09.007