Revision as of 19:34, 1 October 2024

Toehold switch B for detection of hsa-miR-484 with T7 promoter and terminator, and LacZ reporter

MS toehold switch B (BBa_K5106001) under control of a T7 promoter and terminator, regulating expression of a LacZ reporter gene, in order to test the toehold functionality in vitro in a cell-free PURExpress system.

Usage and Biology

This composite part consists of the basic toehold switch part (BBa_K5106002), under control of a T7 promoter and terminator, and the LacZ reporter gene. To test the whether the designed toehold switch works, a plasmid expressing this composite part was made, and expressed in a PURExpress cell-free system. This is a reconstituted form of cell-free expression that works by isolating the necessary components, such as ribosomes and amino acids, purifying them, and assembling them into a reaction mixture.¹

Qualitative in vitro test

To first check whether the toehold switch was activated by the trigger miRNA hsa-miR-484 (BBa_K5106000), we performed a test in 2 μL PURExpress, with ~25 ng plasmid containing the toehold switch (this composite part). Besides other toehold switches during this test, a negative control, containing no DNA template, and a positive control, containing only lacZ under the control of the T7 promoter and terminator, were included as well. In addition, 0.5 μL miRNA hsa-miR-484 (5 μM) was added to part of the samples. The tubes were incubated at 37 °C for two hours.

After two hours, β-galactosidase (LacZ) performed as expected, since no colour change from yellow to purple was observed in the negative control, whereas the colour change was observed in the positive control (Figure 1). This change is caused by For the part containing MS toehold switch B, a clear colour change can also be observed (Figure 1), indicating that the toehold switch can indeed be activated by hsa-miR-484, resulting in further translation of the downstream protein coding region.

Quantitative in vitro test

In addition to this qualitative test, we performed a quantitative measurement to evaluate the performance of the toehold switch. For this 1 μL trigger miRNA (5μM) was added to 5 μL PURExpress containing ~30 ng of DNA template. The tubes were incubated at 37 °C for two hours. Every 20 minutes, a 0.5 μL sample was taken and diluted in 75 μL nuclease free-water. We measured the absorption at 570 nm to measure the product (chlorophenol red), and 415 nm to measure the substrate (Red-β-D-Galactopyranoside) of β-galactosidase, which is translated after activation of the toehold switch.

It can be seen the absorbance at 570 nm increases over time, and that the absorbance at 415 nm decreases over time. This indicates that the MS toehold switch B does indeed work, and gets activated by trigger hsa-miR-484 and can then regulate downstream protein encoding regions. There is also a clear difference observed between the change in signal in the presence or absence of the trigger RNA. This toehold switch is the best working switch designed by miRADAR (WageningenUR 2024).

Sequence and Features

1. Shimizu, Yoshihiro, Akio Inoue, Yukihide Tomari, Tsutomu Suzuki, Takashi Yokogawa, Kazuya Nishikawa, and Takuya Ueda. ‘Cell-Free Translation Reconstituted with Purified Components’. Nature Biotechnology 19, no. 8 (August 2001): 751–55. https://doi.org/10.1038/90802.