Difference between revisions of "Part:BBa K2332014"

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<partinfo>BBa_K2332014 short</partinfo>
 
<partinfo>BBa_K2332014 short</partinfo>
  
This biobrick is the fusion of a truncated version of Intimin (159kDa) and SpyCatcher (138 amino acids, 15 kDa) for the cell surface display of SpyCatcher under the control of our blue light inducible promoter [https://parts.igem.org/wiki/index.php?title=Part:BBa_K2332002 (Pblind)] (see Figure 1). To trigger cell adhesion, we decided to make use of the SpyTag and SpyCatcher, two binding partners that form rapid covalent bonds, fused to outer membrane surface proteins. SpyTag (13 amino acids) and SpyCatcher (138 amino acids, 15 kDa) come from CnaB2 (immunoglobulin-llike collagen adhesin domain) of the FbaB protein, found in the invasive strains of S. pyogenes. We decided to fuse SpyTag and SpyCatcher to outer membrane surface proteins in distinct cell populations that would then aggregate once mixed together post blue light induction.  
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This biobrick is the fusion of a truncated version of Intimin (159kDa), an outer membrane surface protein, and SpyCatcher (138 amino acids, 15 kDa) for the cell surface display of SpyCatcher under the control of our blue light inducible promoter [https://parts.igem.org/wiki/index.php?title=Part:BBa_K2332002 (Pblind)] (see Figure 1). To trigger cell adhesion, we decided to make use of the SpyTag and SpyCatcher, two binding partners that form rapid covalent bonds, fused to outer membrane surface proteins. SpyTag (13 amino acids) and SpyCatcher (138 amino acids, 15 kDa) come from CnaB2 (immunoglobulin-llike collagen adhesin domain) of the FbaB protein, found in the invasive strains of S. pyogenes. The reactive lysine in SpyCatcher forms an isopeptide covalent bond with the aspartate residue in SpyTag. We decided to fuse SpyTag and SpyCatcher to outer membrane surface proteins in distinct cell populations that would then aggregate once mixed together post blue light induction. For blue-light transcriptional induction, cells must also express EL222 ([https://parts.igem.org/Part:BBa_K2332004 BBa_K2332004]).  
  
  
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[[File:Pblind.png|thumb|center|500px| Figure 1: Blue light inducible expression system. Under blue light, the EL222 DNA binding protein dimerises and bind its binding region within the designed Pblind promoter, overlapping the -35 region of the luxI promoter. This ultimately results in the recruitment of RNAP and transcriptional activation of Intimin'-SpyTag or Intimin'-SpyCatcher. Figure adapted from [https://www.ncbi.nlm.nih.gov/pubmed/27353329 Jayaraman P. et al. (2016)]]]
 
[[File:Pblind.png|thumb|center|500px| Figure 1: Blue light inducible expression system. Under blue light, the EL222 DNA binding protein dimerises and bind its binding region within the designed Pblind promoter, overlapping the -35 region of the luxI promoter. This ultimately results in the recruitment of RNAP and transcriptional activation of Intimin'-SpyTag or Intimin'-SpyCatcher. Figure adapted from [https://www.ncbi.nlm.nih.gov/pubmed/27353329 Jayaraman P. et al. (2016)]]]
  
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[[File:Intimin-fusions.png|thumb|center|500px| Figure 2: Cell surface display of SpyTag and SpyCatcher for cell aggregation. Two cell lines are expressing a truncated version of intimin, denoted Intimin', fused to SpyCatcher or SpyTag. Intimin is an outer membrane protein and thus proteins fused to its N termini will be displayed on the cell surface. Once the cell lines come together, the reactive lysine in SpyCatcher will form an isopeptide covalent bond with the aspartate residue in SpyTag and cells will aggregate.]]
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[[File:Pblind-adhesion.png|thumb|center|200px| Figure 3: Blue light induction of cell aggregation. Representation of two cell lines expressing either intimin’-SpyTag or intimin’-SpyCatcher fusion proteins under the control of PBlind pre and post light induction.]]
  
 
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Revision as of 10:30, 24 October 2017


Blue light inducible expression of Intimin'-SpyCatcher (Pblind Intimin'-SpyCatcher)

This biobrick is the fusion of a truncated version of Intimin (159kDa), an outer membrane surface protein, and SpyCatcher (138 amino acids, 15 kDa) for the cell surface display of SpyCatcher under the control of our blue light inducible promoter (Pblind) (see Figure 1). To trigger cell adhesion, we decided to make use of the SpyTag and SpyCatcher, two binding partners that form rapid covalent bonds, fused to outer membrane surface proteins. SpyTag (13 amino acids) and SpyCatcher (138 amino acids, 15 kDa) come from CnaB2 (immunoglobulin-llike collagen adhesin domain) of the FbaB protein, found in the invasive strains of S. pyogenes. The reactive lysine in SpyCatcher forms an isopeptide covalent bond with the aspartate residue in SpyTag. We decided to fuse SpyTag and SpyCatcher to outer membrane surface proteins in distinct cell populations that would then aggregate once mixed together post blue light induction. For blue-light transcriptional induction, cells must also express EL222 (BBa_K2332004).


Usage and Biology

Figure 1: Blue light inducible expression system. Under blue light, the EL222 DNA binding protein dimerises and bind its binding region within the designed Pblind promoter, overlapping the -35 region of the luxI promoter. This ultimately results in the recruitment of RNAP and transcriptional activation of Intimin'-SpyTag or Intimin'-SpyCatcher. Figure adapted from Jayaraman P. et al. (2016)
Figure 2: Cell surface display of SpyTag and SpyCatcher for cell aggregation. Two cell lines are expressing a truncated version of intimin, denoted Intimin', fused to SpyCatcher or SpyTag. Intimin is an outer membrane protein and thus proteins fused to its N termini will be displayed on the cell surface. Once the cell lines come together, the reactive lysine in SpyCatcher will form an isopeptide covalent bond with the aspartate residue in SpyTag and cells will aggregate.
Figure 3: Blue light induction of cell aggregation. Representation of two cell lines expressing either intimin’-SpyTag or intimin’-SpyCatcher fusion proteins under the control of PBlind pre and post light induction.

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 898
    Illegal NgoMIV site found at 1639
  • 1000
    COMPATIBLE WITH RFC[1000]