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Solubis: optimize your protein.
De Baets, Greet; Van Durme, Joost; van der Kant, Rob; Schymkowitz, Joost; Rousseau, Frederic.
Afiliação
  • De Baets G; VIB Switch Laboratory, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, 3000 Leuven, Belgium and Vrije Universiteit Brussel, 1050 Brussels, Belgium.
  • Van Durme J; VIB Switch Laboratory, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, 3000 Leuven, Belgium and Vrije Universiteit Brussel, 1050 Brussels, Belgium.
  • van der Kant R; VIB Switch Laboratory, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, 3000 Leuven, Belgium and.
  • Schymkowitz J; VIB Switch Laboratory, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, 3000 Leuven, Belgium and.
  • Rousseau F; VIB Switch Laboratory, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, 3000 Leuven, Belgium and.
Bioinformatics ; 31(15): 2580-2, 2015 Aug 01.
Article em En | MEDLINE | ID: mdl-25792555
MOTIVATION: Protein aggregation is associated with a number of protein misfolding diseases and is a major concern for therapeutic proteins. Aggregation is caused by the presence of aggregation-prone regions (APRs) in the amino acid sequence of the protein. The lower the aggregation propensity of APRs and the better they are protected by native interactions within the folded structure of the protein, the more aggregation is prevented. Therefore, both the local thermodynamic stability of APRs in the native structure and their intrinsic aggregation propensity are a key parameter that needs to be optimized to prevent protein aggregation. RESULTS: The Solubis method presented here automates the process of carefully selecting point mutations that minimize the intrinsic aggregation propensity while improving local protein stability.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Proteínas / Dobramento de Proteína / Análise de Sequência de Proteína / Mutação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Proteínas / Dobramento de Proteína / Análise de Sequência de Proteína / Mutação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article