Difference between revisions of "Part:BBa K1694013"
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<h1>'''Introduction:'''</h1> | <h1>'''Introduction:'''</h1> | ||
− | [[File:V21.png|200px|thumb|right|'''Fig.1''' | + | [[File:V21.png|200px|thumb|right|'''Fig.1''' OmpA-N-scFv(anti-VEGF)]] |
− | To display the antibody outside the ''E. coli'', we used Lipoprotein-Outer membrane protein A (Lpp-OmpA). According to the paper reference | + | To display the antibody outside the ''E. coli'', we used Lipoprotein-Outer membrane protein A (Lpp-OmpA). According to the paper reference, We chose the first 9 amino acid of Lpp, and the 46~159 amino acid of OmpA. |
<br> | <br> | ||
In order to change the scFv parts easily, we added a ''NcoI'' restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the ''NcoI'' restriction enzyme. | In order to change the scFv parts easily, we added a ''NcoI'' restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the ''NcoI'' restriction enzyme. | ||
<br> | <br> | ||
− | The Fig.2 showed how we combine Lpp-OmpA-N and scFv together, | + | The Fig.2 showed how we combine Lpp-OmpA-N and scFv together. First, we use restriction enzyme ''NcoI'' to digest the upstream and downstream parts. After ligate two digest product, there are no M site in Lpp-OmpA-N-scFv. |
<br> | <br> | ||
<div style="display: block; height: 250pt;"> | <div style="display: block; height: 250pt;"> | ||
− | [[File:131415.png|600px|thumb|left|'''Fig.2''' The combination of | + | [[File:131415.png|600px|thumb|left|'''Fig.2''' The combination of OmpA-N-scFv]] |
− | [[File:ompascfv.png|250px|thumb|left|'''Fig.3''' | + | [[File:ompascfv.png|250px|thumb|left|'''Fig.3''' OmpA-N-scFv]] |
</div> | </div> | ||
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[[File:OB.png|200px|thumb|left|'''Fig.4''' The PCR result of the Lpp-OmpA-N+scFv. The DNA sequence length is around 1000~1200 bp, so the PCR products should appear at 1200~1400 bp.]] | [[File:OB.png|200px|thumb|left|'''Fig.4''' The PCR result of the Lpp-OmpA-N+scFv. The DNA sequence length is around 1000~1200 bp, so the PCR products should appear at 1200~1400 bp.]] | ||
− | After receiving the DNA sequences from the gene synthesis company, we recombined each OmpA-N-scFv gene to PSB1C3 backbones and conducted a PCR experiment to check the size of each of the OmpA-N-scFv. The DNA sequence length of the OmpA-N-scFv is around 1000~1200 | + | After receiving the DNA sequences from the gene synthesis company, we recombined each OmpA-N-scFv gene to PSB1C3 backbones and conducted a PCR experiment to check the size of each of the OmpA-N-scFv. The DNA sequence length of the OmpA-N-scFv is around 1000~1200 b.p. In this PCR experiment, the OmpA-N-scFv products size should be near at 1200~1400 b.p. The Fig.4 showed the correct size of the OmpA-N-scFv, and proved that we successful ligated the scFv sequence onto an ideal backbone. |
− | [[File:OmpA-B.png|600px|thumb|center|'''Fig.5''' OmpA-N-scFv( | + | [[File:OmpA-B.png|600px|thumb|center|'''Fig.5''' OmpA-N-scFv(anti-VEGF)]] |
Revision as of 05:38, 22 September 2015
OmpA-scFv(Anti-VEGF)
Introduction:
To display the antibody outside the E. coli, we used Lipoprotein-Outer membrane protein A (Lpp-OmpA). According to the paper reference, We chose the first 9 amino acid of Lpp, and the 46~159 amino acid of OmpA.
In order to change the scFv parts easily, we added a NcoI restriction site between OmpA and scFv so that we can change various scFv DNA sequence using the NcoI restriction enzyme.
The Fig.2 showed how we combine Lpp-OmpA-N and scFv together. First, we use restriction enzyme NcoI to digest the upstream and downstream parts. After ligate two digest product, there are no M site in Lpp-OmpA-N-scFv.
Experiment:
After receiving the DNA sequences from the gene synthesis company, we recombined each OmpA-N-scFv gene to PSB1C3 backbones and conducted a PCR experiment to check the size of each of the OmpA-N-scFv. The DNA sequence length of the OmpA-N-scFv is around 1000~1200 b.p. In this PCR experiment, the OmpA-N-scFv products size should be near at 1200~1400 b.p. The Fig.4 showed the correct size of the OmpA-N-scFv, and proved that we successful ligated the scFv sequence onto an ideal backbone.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 388
- 1000COMPATIBLE WITH RFC[1000]