Difference between revisions of "Part:BBa K4165015"
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UBE2W enzyme is an E2 ubiquitin-conjugating enzyme that has the ability to recruit the ubiquitin-proteasome pathway. In the wet lab, we cloned it in DH-5 alpha using a pJET cloning vector then we did manual plasmid miniprep to extract the part, and ligate it to be expressed in BL-21 using a pGS-21a expression vector to used in in-vitro ubiquitination assay to prove the concept that our system recruits the 26S proteasomal-ubiquitin cascade. | UBE2W enzyme is an E2 ubiquitin-conjugating enzyme that has the ability to recruit the ubiquitin-proteasome pathway. In the wet lab, we cloned it in DH-5 alpha using a pJET cloning vector then we did manual plasmid miniprep to extract the part, and ligate it to be expressed in BL-21 using a pGS-21a expression vector to used in in-vitro ubiquitination assay to prove the concept that our system recruits the 26S proteasomal-ubiquitin cascade. | ||
<p style=" font-weight: bold; font-size:14px;"> Transformation of His UBE2W in BL-21 using pGS-21a expression vector and in DH-5 alpha using pJET cloning vector</p> | <p style=" font-weight: bold; font-size:14px;"> Transformation of His UBE2W in BL-21 using pGS-21a expression vector and in DH-5 alpha using pJET cloning vector</p> | ||
| − | The transformation was done using the TSS protocol after testing different buffers which are TSS buffer, Calcium Chloride, and a combination between Calcium Chloride and Magnesium Chloride. We optimized our protocol to use the TSS buffer as it showed the best results. The transformation efficiency and CFU/ml were calculated for UBE2W in the pGS-21a expression vector and in the pJET cloning vector and they were found to be 576000 no. of transformants/ug and CFU/ml = 1152000 and 240000 no. of transformants/ug and CFU/ml = 480000 respectively. | + | The transformation was done using the TSS protocol after testing different buffers which are TSS buffer, Calcium Chloride, and a combination between Calcium Chloride and Magnesium Chloride. We optimized our protocol to use the TSS buffer as it showed the best results. The transformation efficiency and CFU/ml were calculated for UBE2W in the pGS-21a expression vector and in the pJET cloning vector and they were found to be 576000 no. of transformants/ug and CFU/ml = 1152000 and 240000 no. of transformants/ug and CFU/ml = 480000 respectively. |
| + | |||
| + | <p style=" font-weight: bold; font-size:14px;"> Transformation of His UBE2W in DH-5 alpha using pJET cloning vector </p> | ||
| + | <html> | ||
| + | <p><img src="https://static.igem.wiki/teams/4165/wiki/parts-registry/wetlab-results/ube2w-pjet.jpg" style="margin-left:200px;" alt="" width="500" /></p></html> | ||
| + | Figure 2. Transformed plate of His UBE2W + pJET | ||
| + | |||
<html> | <html> | ||
<p><img src="https://static.igem.wiki/teams/4165/wiki/parts-registry/wetlab-results/ube2w-pgs.jpg" style="margin-left:200px;" alt="" width="500" /></p> | <p><img src="https://static.igem.wiki/teams/4165/wiki/parts-registry/wetlab-results/ube2w-pgs.jpg" style="margin-left:200px;" alt="" width="500" /></p> | ||
</html> | </html> | ||
| − | Figure | + | Figure 3. Transformed plate of His UBE2W + pGS-21a |
| − | <p style=" font-weight: bold; font-size:14px;"> | + | <p style=" font-weight: bold; font-size:14px;"> Affinity chromatography of Ube2W </p> |
| + | Affinity chromatography is a technique used to purify the proteins to get the protein alone without the cell lysate. So, we performed affinity chromatography for total protein extraction to get pure UBE2W. | ||
<html> | <html> | ||
| − | <p><img src="https://static.igem.wiki/teams/4165/wiki/parts-registry/wetlab-results/ | + | <p><img src="https://static.igem.wiki/teams/4165/wiki/parts-registry/wetlab-results/standard-curve.jpg" style="margin-left:200px;" alt="" width="500" /></p> |
| − | + | </html> | |
| + | <html> | ||
| + | <p><img src="https://static.igem.wiki/teams/4165/wiki/parts-registry/wetlab-results/ube2w.jpg" style="margin-left:200px;" alt="" width="500" /></p> | ||
| + | </html> | ||
| + | Figure 4. This figure shows the BCA assay results of the affinity chromatography that was done after the protein | ||
| + | extraction. | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
Latest revision as of 22:49, 13 October 2022
UBE2W
Ubiquitin-conjugating E2 ligase has a role in the ubiquitination cascade for protein degradation.
Usage and Biology
This E2 ubiquitin-conjugating enzyme UBE2W is the key participant in the set of enzymes as it is responsible for the initial step of monoubiquitylation by the Trim21 E3 ligase. The UBE2W is most specific for RING domain E3 ligases which happens to be that Trim21, which we are working with, is one of those RING domain E3 ligases.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Dry Lab
Mathematical modeling
Transcription rate and translation rate under T7 promotor
the mathematical modeling was based on our code for the calculation of transcription and translation (you can find it in the code section) besides the estimated results from the wet lab.
Figure 1. this figure shows the results from the transcription and translation code showing the
variation of mRNA and protein concentrations with time compared with the wet lab results.
WetLab Results
UBE2W enzyme is an E2 ubiquitin-conjugating enzyme that has the ability to recruit the ubiquitin-proteasome pathway. In the wet lab, we cloned it in DH-5 alpha using a pJET cloning vector then we did manual plasmid miniprep to extract the part, and ligate it to be expressed in BL-21 using a pGS-21a expression vector to used in in-vitro ubiquitination assay to prove the concept that our system recruits the 26S proteasomal-ubiquitin cascade.
Transformation of His UBE2W in BL-21 using pGS-21a expression vector and in DH-5 alpha using pJET cloning vector
The transformation was done using the TSS protocol after testing different buffers which are TSS buffer, Calcium Chloride, and a combination between Calcium Chloride and Magnesium Chloride. We optimized our protocol to use the TSS buffer as it showed the best results. The transformation efficiency and CFU/ml were calculated for UBE2W in the pGS-21a expression vector and in the pJET cloning vector and they were found to be 576000 no. of transformants/ug and CFU/ml = 1152000 and 240000 no. of transformants/ug and CFU/ml = 480000 respectively.
Transformation of His UBE2W in DH-5 alpha using pJET cloning vector
Figure 2. Transformed plate of His UBE2W + pJET
Figure 3. Transformed plate of His UBE2W + pGS-21a
Affinity chromatography of Ube2W
Affinity chromatography is a technique used to purify the proteins to get the protein alone without the cell lysate. So, we performed affinity chromatography for total protein extraction to get pure UBE2W.
Figure 4. This figure shows the BCA assay results of the affinity chromatography that was done after the protein
extraction.
References
1. Stewart, M. D., Ritterhoff, T., Klevit, R. E., & Brzovic, P. S. (2016). E2 enzymes: more than just middle men. Cell research, 26(4), 423-440. 2. Vittal, V., Wenzel, D. M., Brzovic, P. S., & Klevit, R. E. (2013). Biochemical and structural characterization of the ubiquitin-conjugating enzyme UBE2W reveals the formation of a noncovalent homodimer. Cell biochemistry and biophysics, 67(1), 103-110.