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 language | English |
|---|---|
| Pages (from-to) | 2955-2963 |
| Number of pages | 9 |
| Journal | ACS Synthetic Biology |
| Volume | 9 |
| Issue number | 11 |
| DOIs | |
| State | Published - 20 Nov 2020 |
| Externally published | Yes |
Keywords
- Fluorescence
- Green fluorescent protein
- Protein engineering
- Protein-peptide interaction
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