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Human elastin-like polypeptides as a versatile platform for exploitation of ultrasensitive bilirubin detection by UnaG.
Bandiera, Antonella; Corich, Lucia; Tommasi, Silvia; De Bortoli, Marco; Pelizzo, Paola; Stebel, Marco; Paladin, Dino; Passamonti, Sabina.
Afiliação
  • Bandiera A; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Corich L; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Tommasi S; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • De Bortoli M; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Pelizzo P; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Stebel M; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Paladin D; Dino Paladin Company, Trieste, Italy.
  • Passamonti S; Department of Life Sciences, University of Trieste, Trieste, Italy.
Biotechnol Bioeng ; 117(2): 354-361, 2020 02.
Article em En | MEDLINE | ID: mdl-31691952
A new, bifunctional recombinant protein was expressed as the fusion product of human elastin-like polypeptide (HELP) and the bilirubin-binding protein UnaG. The engineered product displays both the HELP-specific property of forming a functional hydrogel matrix and the UnaG-specific capacity of emitting green fluorescence upon ligand binding. The new fusion protein has been proven to be effective at detecting bilirubin in complex environments with high background noise. A cell culture model of the stress response, consisting of bilirubin released in the cell culture medium, was set up to assess the bilirubin-sensing properties of the functional matrix obtained by cross-linking the HELP moiety. Our engineered protein allowed us to monitor cell induction by the release of bilirubin in the culture medium on a nanomolar scale. This study shows that elastin-like protein fusion represents a versatile platform for the development of novel and commercially viable analytical and biosensing devices.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bilirrubina / Proteínas Recombinantes de Fusão / Proteínas de Transporte / Elastina / Corantes Fluorescentes Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Biotechnol Bioeng Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bilirrubina / Proteínas Recombinantes de Fusão / Proteínas de Transporte / Elastina / Corantes Fluorescentes Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Biotechnol Bioeng Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália