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Genetically encoded fluorescent biosensor for rapid detection of protein expression

  • Matthew G. Eason
  • , Antonia T. Pandelieva
  • , Marc M. Mayer
  • , Safwat T. Khan
  • , Hernan G. Garcia
  • , Roberto A. Chica
  • University of Ottawa
  • California Institute for Quantitative Biosciences

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Fluorescent proteins are widely used as fusion tags to detect protein expression in vivo. To become fluorescent, these proteins must undergo chromophore maturation, a slow process with a half-time of 5 to >30 min that causes delays in real-time detection of protein expression. Here, we engineer a genetically encoded fluorescent biosensor to enable detection of protein expression within seconds in live bacteria. This sensor for transiently expressed proteins (STEP) is based on a fully matured but dim green fluorescent protein in which pre-existing fluorescence increases 11-fold in vivo following the specific and rapid binding of a protein tag (Kd 120 nM, kon 1.7 × 105 M-1 s-1). In live E. coli cells, our STEP biosensor enables detection of protein expression twice as fast as the use of standard fluorescent protein fusions. Our biosensor opens the door to the real-time study of short timescale processes in live cells with high spatiotemporal resolution.

Original languageEnglish
Pages (from-to)2955-2963
Number of pages9
JournalACS Synthetic Biology
Volume9
Issue number11
DOIs
StatePublished - 20 Nov 2020
Externally publishedYes

Keywords

  • Fluorescence
  • Green fluorescent protein
  • Protein engineering
  • Protein-peptide interaction

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