Difference between revisions of "Part:BBa K1694024"
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<h1>'''Introduction:'''</h1> | <h1>'''Introduction:'''</h1> | ||
− | [[File:EGFRHALF.png|600px|thumb|center|Pcons+B0034+Lpp-OmpA-N+scFv(Anti-EGFR) ]] | + | [[File:EGFRHALF.png|600px|thumb|center|'''Fig.1''' Pcons+B0034+Lpp-OmpA-N+scFv(Anti-EGFR) ]] |
By ligating the constitutive promoter (BBa_J23101), strong ribosome binding site (BBa_B0034) and Lpp-OmpA-scFv, we were able to display scFv on the E. coli outer membrane continuously. | By ligating the constitutive promoter (BBa_J23101), strong ribosome binding site (BBa_B0034) and Lpp-OmpA-scFv, we were able to display scFv on the E. coli outer membrane continuously. | ||
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<p style="font-size:120%">'''2.Co-transform'''</p> | <p style="font-size:120%">'''2.Co-transform'''</p> | ||
− | [[File:EGFRHALF.png|600px|thumb|center|'''Fig. | + | [[File:EGFRHALF.png|600px|thumb|center|'''Fig.4''' Pcons+RBS+Lpp-OmpA-N+Anti-EGFR]] |
− | [[File:Pcons+RBS+RFP+Ter.png|600px|thumb|center|'''Fig. | + | [[File:Pcons+RBS+RFP+Ter.png|600px|thumb|center|'''Fig.5''' Pcons+RBS+RFP+Ter]] |
− | [[File:GFP2015.png|600px|thumb|center|'''Fig. | + | [[File:GFP2015.png|600px|thumb|center|'''Fig.6''' Pcons+RBS+GFP+Ter]] |
'''Cell staining experiment:''' | '''Cell staining experiment:''' | ||
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Revision as of 02:33, 19 September 2015
Pcons+B0034+Lpp-OmpA-N+scFv(Anti-EGFR)
Introduction:
By ligating the constitutive promoter (BBa_J23101), strong ribosome binding site (BBa_B0034) and Lpp-OmpA-scFv, we were able to display scFv on the E. coli outer membrane continuously.
Having this part, we can co-transform with other parts in order to produce color as the detection signal.
This year we want to provide a customized platform. We provide two libraries of Pcon+RBS+OmpA-scFv and Pcons+RBS+Fluorescence+Ter into E. coli. Therefore, our customers can choose any scfv and any fluorescence protein. Our team will then co-transform the two plasmids, which helps us tailor our product to the wishes of our customers.
Experiment:
1.Cloning
After receiving the DNA sequences from the gene synthesis company, we recombined each scFv gene to PSB1C3 backbones and conducted a PCR experiment to check the size of each of the scFvs. The DNA sequence length of the scFvs are around 600~800 bp. In this PCR experiment, the scFv products size should be near at 850~1050 bp. The Fig. showed the correct size of the scFv, and proved that we successful ligated the scFv sequence onto an ideal backbone.
2.Co-transform
Cell staining experiment:
After cloning the part of anti-EGFR, we were able to co-transform anti-EGFR with different fluorescence protein into our E. coli.
The next step was to prove that our co-transformed product have successfully displayed scFv of anti-EGFR and expressed fluorescence protein.
To prove this, we conducted the cell staining experiment by using the co-transformed E. coli to detect the EGFR in the cancer cell line.
Fig.9 ~ Fig. 12 are our staining results:
Negative control:
There are red and green fluorescent anti-EGFR E. coli stick on the cell’s surfaces as the anti-EGFR probes on E. colis successfully detect and bind with EGFR.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 451
- 1000COMPATIBLE WITH RFC[1000]