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A general strategy to construct small molecule biosensors in eukaryotes.
Feng, Justin; Jester, Benjamin W; Tinberg, Christine E; Mandell, Daniel J; Antunes, Mauricio S; Chari, Raj; Morey, Kevin J; Rios, Xavier; Medford, June I; Church, George M; Fields, Stanley; Baker, David.
Afiliación
  • Feng J; Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, United States.
  • Jester BW; Department of Genetics, Harvard Medical School, Boston, United States.
  • Tinberg CE; Department of Genome Sciences, University of Washington, Seattle, United States.
  • Mandell DJ; Howard Hughes Medical Institute, University of Washington, Seattle, United States.
  • Antunes MS; Department of Biochemistry, University of Washington, Seattle, United States.
  • Chari R; Department of Genetics, Harvard Medical School, Boston, United States.
  • Morey KJ; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, United States.
  • Rios X; Department of Biology, Colorado State University, Fort Collins, United States.
  • Medford JI; Department of Genetics, Harvard Medical School, Boston, United States.
  • Church GM; Department of Biology, Colorado State University, Fort Collins, United States.
  • Fields S; Department of Genetics, Harvard Medical School, Boston, United States.
  • Baker D; Department of Biology, Colorado State University, Fort Collins, United States.
Elife ; 42015 Dec 29.
Article en En | MEDLINE | ID: mdl-26714111
ABSTRACT
Biosensors for small molecules can be used in applications that range from metabolic engineering to orthogonal control of transcription. Here, we produce biosensors based on a ligand-binding domain (LBD) by using a method that, in principle, can be applied to any target molecule. The LBD is fused to either a fluorescent protein or a transcriptional activator and is destabilized by mutation such that the fusion accumulates only in cells containing the target ligand. We illustrate the power of this method by developing biosensors for digoxin and progesterone. Addition of ligand to yeast, mammalian, or plant cells expressing a biosensor activates transcription with a dynamic range of up to ~100-fold. We use the biosensors to improve the biotransformation of pregnenolone to progesterone in yeast and to regulate CRISPR activity in mammalian cells. This work provides a general methodology to develop biosensors for a broad range of molecules in eukaryotes.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes de Fusión / Técnicas Biosensibles / Eucariontes / Biología Molecular Idioma: En Revista: Elife Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Recombinantes de Fusión / Técnicas Biosensibles / Eucariontes / Biología Molecular Idioma: En Revista: Elife Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos