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Protein-based scaffolds for enzyme immobilization.
Zhang, Guoqiang; Schmidt-Dannert, Sarah; Quin, Maureen B; Schmidt-Dannert, Claudia.
Afiliação
  • Zhang G; Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, St. Paul, MN, United States.
  • Schmidt-Dannert S; Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, St. Paul, MN, United States.
  • Quin MB; Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, St. Paul, MN, United States. Electronic address: mbquin@umn.edu.
  • Schmidt-Dannert C; Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, St. Paul, MN, United States. Electronic address: schmi232@umn.edu.
Methods Enzymol ; 617: 323-362, 2019.
Article em En | MEDLINE | ID: mdl-30784408
ABSTRACT
Biocatalysis is emerging as an alternative approach to chemical synthesis of industrially relevant complex molecules. To obtain suitable yields of compounds in a cost-effective manner, biocatalytic reaction cascades must be efficient, robust, and self-sufficient. One approach is to immobilize biocatalysts on a solid support, stabilizing the enzymes and providing optimal microenvironments for reaction sequences. Protein-based scaffolds can be designed as immobilization platforms for biocatalysts, enabling the genetically encoded spatial organization of single enzymes and multistep enzyme cascades. Additionally, protein scaffolds are versatile, are easily adapted, and remain robust under different reaction conditions. In this chapter, we describe methods for the design and production of a self-assembling protein scaffold system for in vitro coimmobilization of biocatalytic cascade enzymes. We provide detailed methods for the characterization of the protein scaffolds, as well as approaches to load biocatalytic cargo enzymes and test activity of immobilized cascades. In addition, we also discuss methods for the development of a scaffold building block toolbox with different surface properties, which could be adapted for a diversity of biocatalysts requiring alternative microenvironments for function.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Salmonella enterica / Enzimas Imobilizadas Idioma: En Revista: Methods Enzymol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Salmonella enterica / Enzimas Imobilizadas Idioma: En Revista: Methods Enzymol Ano de publicação: 2019 Tipo de documento: Article