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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Peptides based on CcdB protein as novel inhibitors of bacterial topoisomerases

Texto completo
Autor(es):
Trovatti, Eliane [1] ; Cotrim, Camila A. [1] ; Garrido, Saulo S. [1] ; Barros, Ronaldo S. [1] ; Marchetto, Reinaldo [1]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] UNESP, Inst Chem, Dept Biochem & Technol Chem, BR-14800900 Araraquara, SP - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: Bioorganic & Medicinal Chemistry Letters; v. 18, n. 23, p. 6161-6164, DEC 1 2008.
Citações Web of Science: 19
Resumo

The ccd toxin-antitoxin system of the F plasmid encodes CcdB, a protein that poisons the essential Escherichia coli DNA gyrase, unique type IIA topoisomerase able to introduce negative supercoils into DNA. Based on CcdB structure, a series of linear peptide analogues were obtained by the solid-phase methodology. One of these peptides (CcdBET2) displayed inhibition of the supercoiling activity of bacterial DNA gyrase with a concentration required for complete inhibition (IC(100) = 10 mu M) lower than the wild type CcdB. For Topo IV, a second type IIA bacterial topoisomerase, CcdBET2 was better inhibited the relaxation activity with an IC100 of 5 mu M (wt CcdB > 10 mu M). The replacement of Gly, present in the three C-terminal amino acid residues, by Glu, abolished the capacity to inhibit the gyrase but not the Topo IV activities. These findings demonstrate that the mechanism by which CcdBET2 inhibits DNA gyrase is different of the mechanism by which inhibits Topo IV. Therefore, CcdBET2 is a new type II topoisomerase inhibitor with specificity for Topo IV. (C) 2008 Elsevier Ltd. All rights reserved. (AU)

Processo FAPESP: 03/04492-3 - Caracterização da inibição da DNA girase empregando análogos peptídicos da toxina bacteriana ccdB e do seu antídoto ccdA
Beneficiário:Reinaldo Marchetto
Modalidade de apoio: Auxílio à Pesquisa - Regular