Insights into Laccase Engineering from Molecular Simulations: Toward a Binding-Focused Strategy

Understanding the molecular determinants of enzyme performance is of primary importance for the rational design of ad hoc mutants. A novel approach, which combines efficient conformational sampling and quick reactivity scoring, is used here to shed light on how substrate oxidation was improved durin...

Descripción completa

Detalles Bibliográficos
Autores: Monza, Emanuele, Lucas, M. Fatima, Camarero, Susana, Alejaldre, Lorea C., Martínez, Ángel T., Guallar, Victor
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:dnet:digitalcsic_::f70ed1057223e2acdd177e44903e47a1
Acceso en línea:http://hdl.handle.net/10261/427682
https://api.elsevier.com/content/abstract/scopus_id/84927918112
Access Level:acceso abierto
Palabra clave:PELE
Copper oxidoreductases
Directed evolution
In silico enzyme engineering
Substrate binding
Substrate oxidation
Descripción
Sumario:Understanding the molecular determinants of enzyme performance is of primary importance for the rational design of ad hoc mutants. A novel approach, which combines efficient conformational sampling and quick reactivity scoring, is used here to shed light on how substrate oxidation was improved during the directed evolution experiment of a fungal laccase (from Pycnoporus cinnabarinus), an industrially relevant class of oxidoreductases. It is found that the enhanced activity of the evolved enzyme is mainly the result of substrate arrangement in the active site, with no important change in the redox potential of the T1 copper. Mutations at the active site shift the binding mode into a more buried substrate position and provide a more favorable electrostatic environment for substrate oxidation. As a consequence, engineering the binding event seems to be a viable way to in silico evolution of oxidoreductases.