Difference between revisions of "Part:BBa K404121"

 
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provided by the iGEM team Freiburg_Bioware 2010. For obtaining a
 
provided by the iGEM team Freiburg_Bioware 2010. For obtaining a
 
modular
 
modular
toolkit, the complex biological system of the Adeno-associated virus
+
toolkit, the complex biological system of the adeno-associated virus
 
serotype 2
 
serotype 2
 
was examined by an exhaustive literature search. Subsequently, the
 
was examined by an exhaustive literature search. Subsequently, the
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  style="font-size: 10pt; line-height: 115%;">The provided
 
  style="font-size: 10pt; line-height: 115%;">The provided
 
tripartite system is independent of a
 
tripartite system is independent of a
superinfection  of Adeno- or herpes simplex viruses since the
+
superinfection  of adeno- or herpes simplex viruses since the
 
genes encoding
 
genes encoding
 
the required helper-proteins are co-transfected. Inside the eukaryotic
 
the required helper-proteins are co-transfected. Inside the eukaryotic
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assembly steps have to be performed.&nbsp; </span></p>
 
assembly steps have to be performed.&nbsp; </span></p>
 
<p class="MsoNormal" style="text-align: justify;"><span
 
<p class="MsoNormal" style="text-align: justify;"><span
  style="font-size: 10pt; line-height: 115%;">The Composite
+
  style="font-size: 10pt; line-height: 115%;">The composite
 
part </span><span style="font-size: 10pt; line-height: 115%;">[AAV2]-left-ITR_pCMV_betaglobin_mCherry_hGH_[AAV2]-right-ITR
 
part </span><span style="font-size: 10pt; line-height: 115%;">[AAV2]-left-ITR_pCMV_betaglobin_mCherry_hGH_[AAV2]-right-ITR
 
provided by the iGEM team Freiburg_Bioware comprises all <i>cis</i>-elements
 
provided by the iGEM team Freiburg_Bioware comprises all <i>cis</i>-elements
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facile detection of transduced cells using flow cytometry or
 
facile detection of transduced cells using flow cytometry or
 
fluorescence
 
fluorescence
microscopy. While mCherry is expressed in the cytosol, mVennus can be detected in nuclei due to the VP1 integrated NLS. </span></p>
+
microscopy. While mCherry is expressed in the cytosol, mVenus can be detected in nuclei due to the VP1 integrated NLS. </span></p>
 
<p class="MsoNormal" style="text-align: justify;"><span
 
<p class="MsoNormal" style="text-align: justify;"><span
 
  style="font-size: 10pt; line-height: 115%;"><img alt=""
 
  style="font-size: 10pt; line-height: 115%;"><img alt=""
 
  src="https://static.igem.org/mediawiki/2010/2/22/Freiburg10_TimeLapse_AAV-293_mVenus%2BGOI_mCherry_390px.gif"></span></p>
 
  src="https://static.igem.org/mediawiki/2010/2/22/Freiburg10_TimeLapse_AAV-293_mVenus%2BGOI_mCherry_390px.gif"></span></p>
<p class="MsoNormal">&nbsp;</p>
+
<p style="float: left; margin: 0px 0px 40px 0px; font-size: 10px;">Movie 1:HT1080: mVenus (nuclei) and mCherry (cytosol) expression</p>
 
</div>
 
</div>
 
</body>
 
</body>

Latest revision as of 12:49, 31 October 2010

[AAV2]-left-ITR_pCMV_betaglobin_mCherry_hGH_[AAV2]-right-ITR


[AAV2-left-ITR_pCMV_betaglobin_mCherry_hGH_[AAV2]-right-ITR ]
Freiburg10 Vectorplasmid composite 3.png
BioBrick Nr. BBa_K404121
RFC standard RFC 10
Requirement pSB1C3
Source pAAV_MCS: provided by Stratagene

mCherry:BBa_J06504

Submitted by [http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]


Freiburg10 Vectorplasmid composite 3.png


















Producing recombinant virus particles for therapeutical applications is, besides specific cell targeting, purification and quantification assays of AAV-2, one intention of the Virus Construction Kit provided by the iGEM team Freiburg_Bioware 2010. For obtaining a modular toolkit, the complex biological system of the adeno-associated virus serotype 2 was examined by an exhaustive literature search. Subsequently, the essential components for AAV-2 particle production were extracted and redesigned to match the iGEM standard.

The provided tripartite system is independent of a superinfection  of adeno- or herpes simplex viruses since the genes encoding the required helper-proteins are co-transfected. Inside the eukaryotic host cell, the DNA sequence containing the inverted terminal repeats (ITRs) is extracted and later encapsidated into the preformed capsids after production of single-stranded DNA. Consequently, this plasmid is known as the vector plasmid (pGOI). Promoter, beta-globin intron and the hGH terminator signal are flanked by the ITRs (ITRs, BBa_K404100 and BBa_K404101) and regulate transgene expression. The vector plasmid containing the desired gene of interest is cotransfected with the RepCap plasmid (BBa_K404001, BBa_K404002 or BBa_K404003) and the pHelper plasmid. To obtain the fully assembled vector plasmid, several assembly steps have to be performed. 

The composite part [AAV2]-left-ITR_pCMV_betaglobin_mCherry_hGH_[AAV2]-right-ITR provided by the iGEM team Freiburg_Bioware comprises all cis-elements required for efficient transgene expression in mammalian cells (polyadenylation terminator: BBa_K404108 and transcription enhancer element: BBa_K404107) and encapsidation into virus particles (ITRs: BBa_K404100 and BBa_K404101). The mCherry coding sequence as gene of interest enables facile detection of transduced cells using flow cytometry or fluorescence microscopy. While mCherry is expressed in the cytosol, mVenus can be detected in nuclei due to the VP1 integrated NLS.

Movie 1:HT1080: mVenus (nuclei) and mCherry (cytosol) expression


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
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 2580