Difference between revisions of "Part:BBa K1586000"

Revision as of 11:31, 19 September 2015

Synthetic toehold riboswitch - J23100

Usage and Biology

A toehold switch is a type of RNA molecule known as a riboregulator/riboswitch. It is able to detect the presence of a specific ssRNA molecule (termed the 'trigger RNA') which has a sequence complementary to its switch region through base pairing. If the correct RNA molecule is detected, the protein coding region of the toehold is expressed.

A toehold switch is unique in comparison to other types of riboswitches as it is completely synthetic, and therefore easier to engineer and standardise. The fact that the toehold switch can be modified means that the switch region can be easily changed to detect any given trigger RNA molecule, and the protein coding region can be swapped for any desired reporter protein most suitable for its application.

As shown by Exeter iGEM 2015, toehold switches can be used to detect specific RNA molecules in a cell-free system. In addition to this, the plasmid DNA encoding the toehold switch can be transformed into cells in order to ascertain whether a gene is being expressed (through detection of its mRNA). The applications of this technology can range from a research tool (e.g. detection of secreted RNA in cell supernatant, detection of gene expression, etc.), through to more commercial/medical applications such as diagnostic testing.

The Part

This part encodes for a synthetic toehold switch which has been modified to be under the control of a standard BBa_J23100 constitutive promoter. Originally, this toehold also contained an illegal PstI site at position 844, however this was removed to allow standardisation into a biobrick.

Characterisation

experimental: </br> </br> In order to characterise that this part works as expected, fluorescence intensity was measured for the expression of K1586000 in a cell free system in the presence of different amounts of trigger RNA, where the plasmid encoding for the toehold was kept constant at 0.5 pmols. Below is a graph showing a positive correlation between amount of trigger RNA (in log10(nanograms) with 0ng normalised to 0) and GFP fluorescence intensity.

"In silico": </br> </br> As well as generating experimental data in the lab, "in silico" data was also generated through the software package NUPACK (http://www.nupack.org/) using free energies. For a full explanation of how this works, please visit http://2015.igem.org/Team:Exeter/Modeling.</br> </br>

The equilibrium concentrations of the different components in our system were determined, along with free energy data for the different structures; the unbound trigger, the unbound toehold and the complex of the two.

[[1]]

After obtaining this, the data was converted to an approximate normal distribution and after normalising these within the range of values, we could use the distribution as a probability distribution. Shown below are these obtained probability distributions based on the free energy data.

File:Https://static.igem.org/mediawiki/2015/d/df/NormalisedBindingProbabilityGraph.png

File:Https://static.igem.org/mediawiki/2015/a/a0/NormalisedSplittingProbability.png

Sequence and Features

Functional Parameters