Difference between revisions of "Part:BBa K3187010"
 
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             <h3>Profile</h3>
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             <h1>Profile</h1>
 
             <table style=“width:80%“>
 
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                 <tr>
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                 <tr>
 
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                     <td><b>Base pairs</b></td>
 
                     <td><b>Base pairs</b></td>
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                     <td>1052</td>
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                     <td>1330</td>
 
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             </table>
 
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             <br>
 
             <br>
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             <h3> Usage and Biology</h3>
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             <h1> Usage and Biology</h1>
 
             <p>mCherry <a href="https://parts.igem.org/Part:BBa_K3187026" target="_blank">(BBa_K3187026)</a> is a red
 
             <p>mCherry <a href="https://parts.igem.org/Part:BBa_K3187026" target="_blank">(BBa_K3187026)</a> is a red
 
                 fluorescent
 
                 fluorescent
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                 can be fused to a protein with a C-terminal LPETGG-Sortase A link <a
 
                 can be fused to a protein with a C-terminal LPETGG-Sortase A link <a
 
                         href="https://parts.igem.org/Part:BBa_K3187019"target="_blank">(BBa_K3187019)</a>
 
                         href="https://parts.igem.org/Part:BBa_K3187019"target="_blank">(BBa_K3187019)</a>
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                 by Sortase A. In order to remove the first methionine in front of the GGGG-Sequence a TEVMV-restriction
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                 by Sortase A. In order to remove the first methionine in front of the GGGG-Sequence a TVMV restriction
 
                 site is cloned in the sequence. By removing the first methionine the linkage of LPETGG and
 
                 site is cloned in the sequence. By removing the first methionine the linkage of LPETGG and
 
                 GGGG-Sequences should work better. We use mCherry as an easily imaged reporter for checking if the
 
                 GGGG-Sequences should work better. We use mCherry as an easily imaged reporter for checking if the
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             <h3> Methods</h3>
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             <h1> Methods</h1>
  
 
             <h4>Purification</h4>
 
             <h4>Purification</h4>
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                 purified with
 
                 purified with
 
                 <a href="#" target="_blank">GE Healthcare ÄKTA Pure machine</a>
 
                 <a href="#" target="_blank">GE Healthcare ÄKTA Pure machine</a>
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                 which is a machine for FPLC. The used affinity tag was Strep-Tag II.
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                 which is a machine for FPLC. The used affinity tag was Strep-Tag II. TVMV protease cleavage was performed over night at 4 °C.
 
             </p>
 
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            <h4>SDS-Page and Western blot</h4>
 
  
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             <h1>Results</h1>
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             <h3>Results</h3>
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<p> For results regarding the part, please visit: <a
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             <h4>Cloning and Expression</h4>
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                     href="https://parts.igem.org/Part:BBa_K3187028"
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            <p>The successful cloning was proven with sanger sequencing and production with a Western blot.
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                    target="_blank">BBa_K3187028</a>.</p>
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                        src=""
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            <p>
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                <b>Figure 1:</b>
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    </p>
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    <h2>References</h2>
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        <li id="cite_note-1">
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        <span class="mw-cite-backlink">
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            <a href="#cite_ref-1">↑</a>
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            <span class="reference-text">
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                Nathan Shaner, Robert Campbell, Paul Steinbach, Ben Giepmans, Amy Palmer and Roger Tsien, Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein, Nature Biotechnology, 2004, 22: 1567-1572
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                <a rel="nofollow" class="external autonumber" href="#https://www.nature.com/articles/nbt1037">[1] </a>
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 15:58, 21 October 2019


TEV Cleavage Site x GGGG-Tag for Sortase-mediated Ligation X mCherry Fluorescence Protein

Profile

Name TVMV-GGGG-mCherry
Base pairs 1330
Molecular weight 29.4 kDa
Origin synthetic, derived from Discosoma sp.
Parts mCherry, GGGG-Sequence, TVMV site, T7 Promoter, lac Operator, RBS, araBAD promoter + RBS, GASPAG Linker, Strep-Tag II, Double Terminator for pDEStara2
Properties Red fluorescent, Ex λ: 587nm, Em λ: 610 nm

Usage and Biology

mCherry (BBa_K3187026) is a red fluorescent protein. Which is a synthetic protein derived from Discosoma sp. by directed evolution. The N-terminal GGGG-sequence (BBa_K3187018) can be fused to a protein with a C-terminal LPETGG-Sortase A link (BBa_K3187019) by Sortase A. In order to remove the first methionine in front of the GGGG-Sequence a TVMV restriction site is cloned in the sequence. By removing the first methionine the linkage of LPETGG and GGGG-Sequences should work better. We use mCherry as an easily imaged reporter for checking if the coupling worked.
The coding sequence was cloned in pDEStara2 vector, containing the sequence of mCherry, a GGGG-sequence, a TVMV restriction site (BBa_K3187020), a GASPAG-Linker (BBa_K3187038), a Strep-Tag II (BBa_K3187025) for Purification, a T7 promoter with lac-operator and an RBS (BBa_K3187029), a T7TE terminator (BBa_K3187032), a Start-Codon (BBa_J70593) and a Stop-Codon (BBa_K2868029). Since pDEStara2 is a vector for dual expression it also contains an araBAD promoter with an RBS (BBa_K3187041) and a Double Terminator (BBa_K3187042). The coding sequence consists of 851 bp which are translated to 260 amino acids.[1]

Methods

Purification

The GGGG-mCherry with TVMV Restrictionsite was heterologously expressed in E.coli BL21 and purified with GE Healthcare ÄKTA Pure machine which is a machine for FPLC. The used affinity tag was Strep-Tag II. TVMV protease cleavage was performed over night at 4 °C.

Results

For results regarding the part, please visit: BBa_K3187028.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 324
    Illegal PstI site found at 1133
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1197
    Illegal PstI site found at 1133
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 239
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 324
    Illegal PstI site found at 1133
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 324
    Illegal PstI site found at 1133
    Illegal AgeI site found at 74
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 56