Difference between revisions of "Part:BBa K2916047"
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<partinfo>BBa_K2916047 short</partinfo> | <partinfo>BBa_K2916047 short</partinfo> | ||
− | This part is used for expression of | + | This part is used for expression of Nucleotide Diphosphate Kinase needed for the OnePot PURE cell-free system. |
<!-- Add more about the biology of this part here--> | <!-- Add more about the biology of this part here--> | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | |||
+ | |||
+ | ===Characterization=== | ||
+ | |||
+ | =='''Expression and purification of NDK'''== | ||
+ | |||
+ | <br/> | ||
+ | |||
+ | NDK 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.<br/><br/> | ||
+ | '''Methods''' | ||
+ | <br/> | ||
+ | |||
+ | NDK was purified using our <html><a style="padding: 0px; margin: 0px;" href="https://www.protocols.io/view/protein-purification-for-onepot-pure-cell-free-sys-8auhsew"> protocol </a></html>. 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 (<i>Lavickova et al, 2019</i>) 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 <html><a style="padding: 0px; margin: 0px;" href="https://www.protocols.io/view/sps-page-protein-electrophoresis-775hrq6"> here</a></html>). | ||
+ | <br/> | ||
+ | |||
+ | <html> | ||
+ | <figure style="text-align:center;"> | ||
+ | <img style="max-width:700px;" src="https://2019.igem.org/wiki/images/b/bb/T--EPFL--ProteinMolec.png" alt="control"> | ||
+ | <figcaption><b>Figure 1:</b> SDS-PAGE of OnePot PURE protein solution.</figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
+ | |||
+ | '''Conclusion''' | ||
+ | <br/> NDK has a molecular weight of around 17kDa, and since there is a band shown at this level of molecular weight, we may assume that it is expressed. To verify the functionality of this protein we need to proceed with more experiments that would be mainly focused on the efficiency of the system. | ||
+ | <br/> | ||
+ | <br/> | ||
+ | |||
+ | =='''OnePot PURE functionality test'''== | ||
+ | |||
+ | |||
+ | <br/> | ||
+ | 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. <br/> | ||
+ | |||
+ | '''Methods'''<br/> | ||
+ | |||
+ | We expressed <html><a style="padding: 0px; margin: 0px;" href="https://parts.igem.org/Part:BBa_I746909"> superfolding GFP</a></html> following the <html><a style="padding: 0px; margin: 0px;" href="https://www.protocols.io/view/protein-expression-in-onepot-pure-cell-free-system-8avhse6"> protocol</a></html> 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. | ||
+ | <br/> | ||
+ | |||
+ | |||
+ | <html> | ||
+ | <figure style="text-align:center;"> | ||
+ | <img style="max-width:700px;" src="https://2019.igem.org/wiki/images/b/b2/T--EPFL--resultsOnePot10.png" alt="control"> | ||
+ | <figcaption><b>Figure 2:</b> sf GFP expression using 10nM DNA template.</figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
+ | <html> | ||
+ | <figure style="text-align:center;"> | ||
+ | <img style="max-width:700px;" src="https://2019.igem.org/wiki/images/7/75/T--EPFL--resultsOnePot5.png" alt="control"> | ||
+ | <figcaption><b>Figure 3:</b> sf GFP expression using 5nM DNA template.</figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
+ | <html> | ||
+ | <figure style="text-align:center;"> | ||
+ | <img style="max-width:700px;" src="https://2019.igem.org/wiki/images/e/e7/T--EPFL--resultsOnePot25.png" alt="control"> | ||
+ | <figcaption><b>Figure 4:</b> sf GFP expression using 2.5nM DNA template.</figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
+ | <html> | ||
+ | <figure style="text-align:center;"> | ||
+ | <img style="max-width:700px;" src="https://2019.igem.org/wiki/images/7/70/T--EPFL--resultsOnePot.png" alt="control"> | ||
+ | <figcaption><b>Figure 5:</b> Comparison between OnePot PURE and PURExpress at saturation.</figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
+ | |||
+ | '''Conclusion''' | ||
+ | <br/> The expression was successful so we can confirm that NDK exists in our protein solution and is also functioning properly. | ||
+ | <br/> | ||
+ | |||
+ | |||
+ | |||
+ | |||
Used in OnePot PURE | Used in OnePot PURE |
Revision as of 19:46, 21 October 2019
Expression of NDK in E.coli
This part is used for expression of Nucleotide Diphosphate Kinase needed for the OnePot PURE cell-free system.
Usage and Biology
Characterization
Expression and purification of NDK
NDK 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
NDK 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
NDK has a molecular weight of around 17kDa, and since there is a band shown at this level of molecular weight, we may assume that it is expressed. To verify the 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 NDK exists in our protein solution and is also functioning properly.
Used in OnePot PURE Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 140
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]