Difference between revisions of "Part:BBa K883705"
 
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[[Image:Gfpcoilhistag.PNG|300px|center|thumb|<p align="justify">''Figure 4: protein folding prediction of GFP (green) with a His-tag (blue) fused to a coiled coil (purple)]]
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[[Image:Gfpcoilhistag.PNG|300px|center|thumb|<p align="justify">''Figure 2: protein folding prediction of GFP (green) with a His-tag (blue) fused to a coiled coil (purple)</p>]]
  
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The funcionality of the GFP in the fusion protein was tested and confirmed by observing fluorescence when exposing to UV light.
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[[Image:Fluorescence Cbb.png|370px|right|thumb|<p align="justify">''Figure 4: BBa_K883705 in DH5α [right; back] exposed to UV light. In the middle: control colony that does not produce fluorescence. On the front/left: [https://parts.igem.org/wiki/index.php?title=Part:BBa_K883704 BBa_K883704] in DH5α'</p>]]
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[[Image:Fluorescence bricks .jpg|500px|left|thumb|<p align="justify">''Figure 3: fluorescence GFPcoil + IPTG induced promter in pSB1AK3 in BL21, GFPcoil + His tag + IPTG induced promoter in pSB1AK3 in JM109, [https://parts.igem.org/wiki/index.php?title=Part:BBa_K883704 BBa_K883704] in DH5α, BBa_K883705 in DH5α measured with fluorescence microscopy. On the right side: before induction (sample taken from liquid medium); on the left side: after induction with IPTG (sample taken from a plate) - of each sample a picture was taken once with light microscopy and once with fluorescence microscopy'</p>]]
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<html><div style="clear:both;height:1px;"></div></html>
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To be able to use the device, the counterpart of the E-coil needs to be fused to the protein that needs to be detected.
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{| class="wikitable" style="text-align: center"
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|- style="font-style: italic"
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|name
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|sequence 
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|translated 
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|-
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|K-coil (counterpart)
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|aagatagcggcgttgaaggagaaaatcgcagcactaaaagaaaagatagcggcgttgaaggag   
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|KIAALKEKIAALKEKIAALKE     
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|-
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|E-coil (present in the brick)   
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|gaaattgcggcgctggaaaaagaaattgcggcgctggaaaaagaaattgcggcgctggaaaaa     
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|EIAALEKEIAALEKEIAALEK     
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|}
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===Source===
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The biobrick [https://parts.igem.org/Part:BBa_I13522 BBa_I13522] was used as a template for the mutations.
  
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===Usage and Biology===
 
  
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K883703 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K883705 SequenceAndFeatures</partinfo>
  
  
 
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===Functional Parameters===
 
===Functional Parameters===
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<partinfo>BBa_K883703 parameters</partinfo>
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<partinfo>BBa_K883705 parameters</partinfo>
 
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Latest revision as of 14:46, 26 October 2012

Figure 1: cross-section view of a E-/ K-coil heterodimer'


IPTG induced promoter + GFP with a His-tag fused to a coiled coil

GFP with His tag at the C-terminus and the E-coil at the N-terminus behind an IPTG induced promoter to use it as reporter for the E- and K-coil [http://2012.igem.org/Team:Wageningen_UR/Coil_system Plug and Apply system]

Usage and Biology

The E-coil present in this reporter protein is one part of the Plug and Apply (PnA) system consisting of a combination of E- and K-coil. These coils consist of α-helical repeats and have a strong affinity to each other due to electrostatic interactions (with K-coil positively charged and E-coil negatively charged). Using this system one can bind two proteins noncovalently but specifically to each other. This brick can be used for confirmation of the Plug and Apply system using E- and K-coils as well as for detection of proteins that can be fused to the K-coil.

Figure 2: protein folding prediction of GFP (green) with a His-tag (blue) fused to a coiled coil (purple)

The funcionality of the GFP in the fusion protein was tested and confirmed by observing fluorescence when exposing to UV light.

Figure 4: BBa_K883705 in DH5α [right; back] exposed to UV light. In the middle: control colony that does not produce fluorescence. On the front/left: BBa_K883704 in DH5α'

Figure 3: fluorescence GFPcoil + IPTG induced promter in pSB1AK3 in BL21, GFPcoil + His tag + IPTG induced promoter in pSB1AK3 in JM109, BBa_K883704 in DH5α, BBa_K883705 in DH5α measured with fluorescence microscopy. On the right side: before induction (sample taken from liquid medium); on the left side: after induction with IPTG (sample taken from a plate) - of each sample a picture was taken once with light microscopy and once with fluorescence microscopy'



To be able to use the device, the counterpart of the E-coil needs to be fused to the protein that needs to be detected.


name sequence translated
K-coil (counterpart) aagatagcggcgttgaaggagaaaatcgcagcactaaaagaaaagatagcggcgttgaaggag KIAALKEKIAALKEKIAALKE
E-coil (present in the brick) gaaattgcggcgctggaaaaagaaattgcggcgctggaaaaagaaattgcggcgctggaaaaa EIAALEKEIAALEKEIAALEK

Source

The biobrick BBa_I13522 was used as a template for the mutations.


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 233
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 233
    Illegal NotI site found at 239
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 233
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 233
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 233
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1041