Difference between revisions of "Part:BBa K404202"
 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K404202 short</partinfo>
 
<partinfo>BBa_K404202 short</partinfo>
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{| style="color:black" cellpadding="6" cellspacing="1" border="2" align="left"
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! colspan="2" style="background:#66bbff;"|[https://parts.igem.org/Part:BBa_K404202 ViralBrick-453-His-Tag]
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|-
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|'''BioBrick Nr.'''
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|[https://parts.igem.org/Part:BBa_K404165 BBa_K404202]
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|-
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|'''RFC standard'''
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|[https://parts.igem.org/Help:Assembly_standard_25 RFC 25]
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|-
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|'''Requirement'''
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|pSB1C3<br>
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|-
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|'''Source'''
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|
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|-
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|'''Submitted by'''
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|[http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]
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|}
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<br/><br/><br/><br/><br/><br/><br/><br/><br/><br/><br/><br/><br/>
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<br><b>The His-tag motif, ready for insertion into the 453 loop</b>
  
 
[[Image:Freiburg10_ViralBrick-logo-453-His.png|thumb|center|480px]]<br>
 
[[Image:Freiburg10_ViralBrick-logo-453-His.png|thumb|center|480px]]<br>
  
  
−
<!-- Add more about the biology of this part here
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<!-- Add more about the biology of this part here -->
 
===Usage and Biology===
 
===Usage and Biology===
 
Protein tagging via histidine tags is a widely used method for protein purification: Multiple histidine residues (most commonly: Six) are fused to the end of the targeting protein.<br>
 
Protein tagging via histidine tags is a widely used method for protein purification: Multiple histidine residues (most commonly: Six) are fused to the end of the targeting protein.<br>
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Since the aim behind engineering therapeutic AAV vectors is a safe administration to human patients, it is important to consider a convenient way of purifying the virus particles. Contamination by cellular proteins could cause toxic side effects or a strong immune response. Koerber et al. have first inserted a His-tag into a surface-exposed loop at amino acid position 587 in the Cap protein and successfully purified recombinant virsuses using IMAC (Koerber et al. 2007). For our Virus Construction Kit, we provide the His-tag motif in the ViralBrick standard, allowing for an easy insertion into the 453 and/or 587 loop .<br>
 
Since the aim behind engineering therapeutic AAV vectors is a safe administration to human patients, it is important to consider a convenient way of purifying the virus particles. Contamination by cellular proteins could cause toxic side effects or a strong immune response. Koerber et al. have first inserted a His-tag into a surface-exposed loop at amino acid position 587 in the Cap protein and successfully purified recombinant virsuses using IMAC (Koerber et al. 2007). For our Virus Construction Kit, we provide the His-tag motif in the ViralBrick standard, allowing for an easy insertion into the 453 and/or 587 loop .<br>
  
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https://static.igem.org/mediawiki/parts/5/59/Freiburg10_ViralBrick_motif_His.png
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===Restriction sites===
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<table border="1" style="float:right; width:480px; height:auto;>
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<tr>
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  <th><b>Restriction site</b></th>
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  <th><b>Enzyme</b></th>
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  <th><b>Recognition sequence</b></th>
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  <th><b>Activity</b></th>
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  <th><b>Temp.</b></th>
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</tr>
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<tr>
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  <td>upstream 453</td>
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  <td>[http://www.neb.com/nebecomm/products/productR3132.asp SspI-HF]</td>
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  <td>[[image:Freiburg10_recognition site SspI-HF.Gif]]</td>
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  <td>25;100;0;100</td>
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<td>37°C</td>
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</tr>
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<tr>
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  <td>downstream 453</td>
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  <td>[http://www.neb.com/nebecomm/products/productR3138.asp SalI-HF]</td>
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  <td>[[image:Freiburg10_recognition site SalI-HF.Gif]]</td>
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  <td>10;100;100;100</td>
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  <td>37°C</td>
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<tr>
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</table>
  
 
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Latest revision as of 02:17, 28 October 2010

ViralBrick-453-His-Tag

ViralBrick-453-His-Tag
BioBrick Nr. BBa_K404202
RFC standard RFC 25
Requirement pSB1C3
Source
Submitted by [http://2010.igem.org/Team:Freiburg_Bioware FreiGEM 2010]















The His-tag motif, ready for insertion into the 453 loop

Freiburg10 ViralBrick-logo-453-His.png


Usage and Biology

Protein tagging via histidine tags is a widely used method for protein purification: Multiple histidine residues (most commonly: Six) are fused to the end of the targeting protein.
The high binding affinity of histidine towards metal is being exploited for the purification of proteins via the so called “Immobilized Metal Ion Affinity Chromatography“(IMAC): Multiple histidine residues (most commonly: Six) are being fused to the end of the targeting protein. A cell extract containing the recombinant protein is then applied to a column containing immobilized Ni2+-ions. The His-tags complex the Ni2+-ions while other cellular proteins can be washed off the column. The purified proteins can then be eluted with imidazole, which displaces the histidine residues.(Smith, Furman, Ingolia, & Pidgeon, 1988), (Hoffmann & Roeder, 1991)
Since the aim behind engineering therapeutic AAV vectors is a safe administration to human patients, it is important to consider a convenient way of purifying the virus particles. Contamination by cellular proteins could cause toxic side effects or a strong immune response. Koerber et al. have first inserted a His-tag into a surface-exposed loop at amino acid position 587 in the Cap protein and successfully purified recombinant virsuses using IMAC (Koerber et al. 2007). For our Virus Construction Kit, we provide the His-tag motif in the ViralBrick standard, allowing for an easy insertion into the 453 and/or 587 loop .

Freiburg10_ViralBrick_motif_His.png

Restriction sites

Restriction site Enzyme Recognition sequence Activity Temp.
upstream 453 [http://www.neb.com/nebecomm/products/productR3132.asp SspI-HF] Freiburg10 recognition site SspI-HF.Gif 25;100;0;100 37°C
downstream 453 [http://www.neb.com/nebecomm/products/productR3138.asp SalI-HF] Freiburg10 recognition site SalI-HF.Gif 10;100;100;100 37°C

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
    COMPATIBLE WITH RFC[1000]