Molecular determinants of improved cathepsin B inhibition by new cystatins obtained by DNA shuffling

Autor(es)

Valadares, Napoleao F. ; Dellamano, Marcia ; Soares-Costa, Andrea ; Henrique-Silva, Flavio ; Garratt, Richard C.

• Tipo de documento: Artigo Científico
• Fonte: BMC STRUCTURAL BIOLOGY; v. 10, p. 9-pg., 2010-09-30.

Resumo

Background: Cystatins are inhibitors of cysteine proteases. The majority are only weak inhibitors of human cathepsin B, which has been associated with cancer, Alzheimer's disease and arthritis. Results: Starting from the sequences of oryzacystatin-1 and canecystatin-1, a shuffling library was designed and a hybrid clone obtained, which presented higher inhibitory activity towards cathepsin B. This clone presented two unanticipated point mutations as well as an N-terminal deletion. Reversing each point mutation independently or both simultaneously abolishes the inhibitory activity towards cathepsin B. Homology modeling together with experimental studies of the reverse mutants revealed the likely molecular determinants of the improved inhibitory activity to be related to decreased protein stability. Conclusion: A combination of experimental approaches including gene shuffling, enzyme assays and reverse mutation allied to molecular modeling has shed light upon the unexpected inhibitory properties of certain cystatin mutants against Cathepsin B. We conclude that mutations disrupting the hydrophobic core of phytocystatins increase the flexibility of the N-terminus, leading to an increase in inhibitory activity. Such mutations need not affect the inhibitory site directly but may be observed distant from it and manifest their effects via an uncoupling of its three components as a result of increased protein flexibility. (AU)

• Processo FAPESP: 08/58316-5 - Estudos cineticos e funcionais das proteinas humanas da familia septina
• Beneficiário: Napoleão Fonseca Valadares
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 05/59833-5 - Desenvolvimento de canas-de-acucar transgenicas superexpressando cistatinas visando o aumento da resistencia a insetos.
• Beneficiário: Andrea Soares da Costa Fuentes
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 98/14138-2 - Center for Structural Molecular Biotechnology
• Beneficiário: Glaucius Oliva
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs