Difference between revisions of "Part:BBa K1694014"

 
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<h1>'''Introduction:'''</h1>
 
<h1>'''Introduction:'''</h1>
  
To display the antibody outside the E.coli, we used Lipoprotein-Outer membrane protein A (Lpp-OmpA). According to the paper reference [1], We chose the first 9 amino acid of Lpp, and the 46~159 amino acid of OmpA.
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[[File:EG14.png|200px|thumb|right|'''Fig.1''' OmpA-N-scFv(Anti-EGFR)]]
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To display <html><a href="https://parts.igem.org/Part:BBa_K1694004">scFv</a></html> outside the ''E. coli'', we used <html><a href="https://parts.igem.org/Part:BBa_K1694002">Lipoprotein-Outer membrane protein A</a></html> (Lpp-OmpA). According to the paper reference, we chose the first 9 amino acid of Lpp and the 46~159 amino acid of OmpA. When designing ''XbaI-SpeI'' restriction site between Lpp-OmpA and scFv, it will cause a mixed site. Therefore, the ''NcoI'' restriction site rather than the EX-SP restriction site was designed.
 
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<br>
In order to change the scFv parts easily, we added a NcoI restriction site between OmpA and scFv so that we can change vario us scFv DNA sequence using the NcoI restriction enzyme.
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In order to easily change various scFv DNA sequence, we added a ''NcoI'' restriction site between OmpA and scFv.<br>
[[File:ompascfv.png|400px|thumb|center|'''Fig.2''' ompascfv]]
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The Fig.2 showed how we design Lpp-OmpA-N and scFv into ''NcoI'' restriction site. First, we digest Lpp-OmpA part with ''EcoRI'' and ''NcoI'', scFv part with ''NcoI'' and ''PstI.'' Then we ligated them together.  
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<br>
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[[File:131415.png|600px|thumb|left|'''Fig.2''' The combination of OmpA-N-scFv]]
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[[File:ompascfv.png|250px|thumb|left|'''Fig.3''' OmpA-N-scFv]]
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<html>
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Introduction of basic parts:
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<br>
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<a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K1694004"> Anti-EGFR </a><br>
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</html>
  
  
 
<h1>'''Experiment:'''</h1>
 
<h1>'''Experiment:'''</h1>
[[File:OC.png|200px|thumb|left|'''Fig.3'''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.]]  
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[[File:OC.png|200px|thumb|left|'''Fig.4''' The PCR result of the Lpp-OmpA-N+scFv. The length of DNA sequence is 1181 bp, so the PCR products should appear at 1200~1400 bp.]]  
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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 OmpA-N-scFv. The length of OmpA-N-scFv DNA sequence is 1181 bp. In this PCR experiment, OmpA-N-scFv products size should be near at 1200~1400 bp. The Fig.4 showed the correct size of the scFv, and proved that we successfully ligated the scFv sequence onto an ideal backbone.
  
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-scFvs. The DNA sequence length of the OmpA-N-scFvs are around 1000~1200 bp. In this PCR experiment, the OmpA-N-scFv products size should be near at 1200~1400 bp. The Fig. showed the correct size of the scFv, and proved that we successful ligated the scFv sequence onto an ideal backbone.
 
  
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[[File:OmpA-C.png|600px|thumb|center|'''Fig.5''' OmpA-N-scFv(Anti-EGFR)]]
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 07:48, 22 September 2015

OmpA-scFv(Anti-EGFR)

Introduction:


Fig.1 OmpA-N-scFv(Anti-EGFR)

To display scFv 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. When designing XbaI-SpeI restriction site between Lpp-OmpA and scFv, it will cause a mixed site. Therefore, the NcoI restriction site rather than the EX-SP restriction site was designed.
In order to easily change various scFv DNA sequence, we added a NcoI restriction site between OmpA and scFv.
The Fig.2 showed how we design Lpp-OmpA-N and scFv into NcoI restriction site. First, we digest Lpp-OmpA part with EcoRI and NcoI, scFv part with NcoI and PstI. Then we ligated them together.


Fig.2 The combination of OmpA-N-scFv
Fig.3 OmpA-N-scFv


Introduction of basic parts:
Anti-EGFR


Experiment:

Fig.4 The PCR result of the Lpp-OmpA-N+scFv. The length of DNA sequence is 1181 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 OmpA-N-scFv. The length of OmpA-N-scFv DNA sequence is 1181 bp. In this PCR experiment, OmpA-N-scFv products size should be near at 1200~1400 bp. The Fig.4 showed the correct size of the scFv, and proved that we successfully ligated the scFv sequence onto an ideal backbone.


Fig.5 OmpA-N-scFv(Anti-EGFR)

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 388
  • 1000
    COMPATIBLE WITH RFC[1000]