Cell-free transcription-translation system: a dual read-out assay to characterize riboswitch function.
Jasleen Kaur BainsNusrat Shahin QureshiBetül CeylanAnna WackerHarald SchwalbePublished in: Nucleic acids research (2023)
Cell-free protein synthesis assays have become a valuable tool to understand transcriptional and translational processes. Here, we established a fluorescence-based coupled in vitro transcription-translation assay as a read-out system to simultaneously quantify mRNA and protein levels. We utilized the well-established quantification of the expression of shifted green fluorescent protein (sGFP) as a read-out of protein levels. In addition, we determined mRNA quantities using a fluorogenic Mango-(IV) RNA aptamer that becomes fluorescent upon binding to the fluorophore thiazole orange (TO). We utilized a Mango-(IV) RNA aptamer system comprising four subsequent Mango-(IV) RNA aptamer elements with improved sensitivity by building Mango arrays. The design of this reporter assay resulted in a sensitive read-out with a high signal-to-noise ratio, allowing us to monitor transcription and translation time courses in cell-free assays with continuous monitoring of fluorescence changes as well as snapshots of the reaction. Furthermore, we applied this dual read-out assay to investigate the function of thiamine-sensing riboswitches thiM and thiC from Escherichia coli and the adenine-sensing riboswitch ASW from Vibrio vulnificus and pbuE from Bacillus subtilis, which represent transcriptional and translational on- and off-riboswitches, respectively. This approach enabled a microplate-based application, a valuable addition to the toolbox for high-throughput screening of riboswitch function.
Keyphrases
- cell free
- single molecule
- high throughput
- living cells
- transcription factor
- binding protein
- escherichia coli
- circulating tumor
- gold nanoparticles
- label free
- bacillus subtilis
- sensitive detection
- quantum dots
- protein protein
- gene expression
- amino acid
- poor prognosis
- crispr cas
- magnetic nanoparticles
- biofilm formation
- cystic fibrosis
- nucleic acid
- heat shock
- small molecule
- pseudomonas aeruginosa
- oxidative stress
- staphylococcus aureus