Difference between revisions of "Part:BBa K2916049"

Latest revision as of 03:39, 22 October 2019

Expression of T7 RNA in E.coli

This part is used for expression of T7 RNA Polymerase (T7 RNAP) needed for the OnePot PURE cell-free system.

Usage and Biology

T7 RNA Polymerase is one of the most important components of the PURE system, which allows us to transcribe DNA sequences that have a T7 promoter to mRNA which subsequently will then be translated.

In our project we used T7 RNAP as a part of the protein solution needed for OnePot PURE cell-free system produced with the method of gravity flow affinity chromatography, as described in the protocol we designed.

Characterization

Expression and purification of T7 RNAP

T7 RNAP is one of the proteins we used for the OnePot PURE cell-free system. We expressed it in M15 E.coli strain using a pQE30 vector. The expression system has a T5 lac operator, RBS and a lambda t0 Terminator, enabling us to regulate the expression with IPTG.

Methods

T7 RNAP was purified using our protocol . To test if the protein was actually expressed, we performed a SDS-PAGE that is presented below. On the left side we can see the results included in the initial OnePot PURE paper (Lavickova et al, 2019) while on the right (batch1_a,b and batch2_a,b) are the solutions we produced ourselves. (The procedure we followed and the conditions of the experiment can be found here).

Conclusion
T7 RNAP has a molecular weight of around 96kDa, but even though we cannot be absolutely sure if the band shown is only due to it, we may assume that it is expressed. To verify the existence and functionality of this protein we need to proceed with more experiments that would be mainly focused on the efficiency of the system.

OnePot PURE functionality test

To make sure that we have all the proteins in our OnePot PURE protein solution, and that they all function properly we need check if proteins can be expressed in our OnePot PURE cell-free system.

Methods

We expressed superfolding GFP following the protocol we designed in 10μl reactions, and measured the fluorescence on a plate reader at excitation wavelength of 535nm. We tested the expression using different concentrations of the sf GFP DNA template and also compared it with the fluorescence produced in PURExpress from NEB.

Conclusion
The expression was successful so we can confirm that T7 RNAP exists in our protein solution and is also functioning properly.

Sequence and Features