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An optogenetic gene expression system with rapid activation and deactivation kinetics.
Motta-Mena, Laura B; Reade, Anna; Mallory, Michael J; Glantz, Spencer; Weiner, Orion D; Lynch, Kristen W; Gardner, Kevin H.
Afiliación
  • Motta-Mena LB; 1] Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA. [2] Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Reade A; 1] Cardiovascular Research Institute, University of California-San Francisco, San Francisco, California, USA. [2] Department of Biochemistry and Biophysics, University of California-San Francisco, San Francisco, California, USA.
  • Mallory MJ; Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Glantz S; Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Weiner OD; 1] Cardiovascular Research Institute, University of California-San Francisco, San Francisco, California, USA. [2] Department of Biochemistry and Biophysics, University of California-San Francisco, San Francisco, California, USA.
  • Lynch KW; Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Gardner KH; 1] Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA. [2] Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, USA. [3] Structural Biology Initiative, Advanced Science Research Center, City University of New York, New
Nat Chem Biol ; 10(3): 196-202, 2014 Mar.
Article en En | MEDLINE | ID: mdl-24413462
ABSTRACT
Optogenetic gene expression systems can control transcription with spatial and temporal detail unequaled with traditional inducible promoter systems. However, current eukaryotic light-gated transcription systems are limited by toxicity, dynamic range or slow activation and deactivation. Here we present an optogenetic gene expression system that addresses these shortcomings and demonstrate its broad utility. Our approach uses an engineered version of EL222, a bacterial light-oxygen-voltage protein that binds DNA when illuminated with blue light. The system has a large (>100-fold) dynamic range of protein expression, rapid activation (<10 s) and deactivation kinetics (<50 s) and a highly linear response to light. With this system, we achieve light-gated transcription in several mammalian cell lines and intact zebrafish embryos with minimal basal gene activation and toxicity. Our approach provides a powerful new tool for optogenetic control of gene expression in space and time.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Expresión Génica / Factores de Transcripción Activadores / Optogenética / Luz Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nat Chem Biol Asunto de la revista: BIOLOGIA / QUIMICA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Expresión Génica / Factores de Transcripción Activadores / Optogenética / Luz Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nat Chem Biol Asunto de la revista: BIOLOGIA / QUIMICA Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos