Difference between revisions of "Part:BBa K5382120"

 
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<partinfo>BBa_K5382120 short</partinfo>
 
<partinfo>BBa_K5382120 short</partinfo>
  
InaK is a kind of ice nucleoprotein of Pseudomonas syringae KCTC1832. Ice nucleoprotein is a kind of protein that can promote the formation of ice crystals in organisms. Its N-terminal domain can be tightly anchored to the surface of E. coli cells as an anchor moda, so as to enable surface display.
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The InaK is a kind of ice nucleoprotein of <i>Pseudomonas syringae</i> KCTC1832. Ice nucleoprotein is a kind of protein that can promote the formation of ice crystals in organisms. Its N-terminal domain can be tightly anchored to the surface of <i>E. coli</i> cells as an anchor moda, so as to enable surface display.<br>
linker here is a short peptide sequence used to link InaK and Im7.
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The linker here is a short peptide sequence used to link InaK and Im7.<br>
Im7 is an immune protein that has a high affinity with CL7(an engineered variant of colicin CE7).Through their high affinity, InaK-linker-Im7 can be tightly bound to CL7-Linker-SFGFP (another composite part we registered) and InaK in CL7-Linker-SFGFP can be tightly anchored to the cell membrane, thus anchoring the entire system to the membrane surface. Finally, the Inak-linker-Im7-CL7-linker-sfGFP system is displayed on the surface of the membrane.sfGFP is a green fluorescent protein. In this system, sfGFP can verify the success of anchoring, and then it can be replaced with single-chain antibodies, nano-antibodies, etc., to play a targeting role. It should be noted that the system we designed uses the high affinity of CL7 and Im7, so some components can be flexibly replaced according to needs, and are suitable for different use scenarios according to different needs. For example, according to different cells to replace the ice nucleated protein, according to different targeting targets to replace sfGFP with different single-chain antibodies, nano antibodies and so on.
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The Im7 is an immune protein that has a high affinity with CL7(an engineered variant of colicin CE7).Through their high affinity, CL7-linker-sfGFP (another composite part we registered) can be tightly bound to InaK-linker-Im7 and the InaK in CL7-linker-sfGFP can be tightly anchored to the cell membrane, thus anchoring the entire system to the membrane surface. Finally, the InaK-linker-Im7-CL7-linker-sfGFP system is displayed on the surface of the membrane(Figure 1).Additionally, the sfGFP is a green fluorescent protein. In this system, sfGFP can be used to verify the anchoring of the system through fluorescence confocal experiments (for details, please refer to the engineering section).<br>
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After validation is completed, replacing sfGFP with targeting elements such as single-chain antibodies can achieve targeting functions. It should be noted that our designed system utilizes the high affinity of CL7 and Im7, so some components can be flexibly replaced according to needs, suitable for different usage scenarios. For example, we can replace the ice nucleation protein with different ones for different cells, and replace sfGFP with different single-chain antibodies, nanobodies, etc., according to different targeting targets.<br>
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<center>https://static.igem.wiki/teams/5382/part-pictures/im7-cl7.png</center><br><center>'''Figure 1.''' Schematic diagram of the targeting plug-in pairing system for Im7 protein to CL7 fusion pair displayed on the EcN surface.</center>
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 12:42, 2 October 2024


InaK-linker-Im7_Cell membrane anchoring protein and immune protein complex

The InaK is a kind of ice nucleoprotein of Pseudomonas syringae KCTC1832. Ice nucleoprotein is a kind of protein that can promote the formation of ice crystals in organisms. Its N-terminal domain can be tightly anchored to the surface of E. coli cells as an anchor moda, so as to enable surface display.
The linker here is a short peptide sequence used to link InaK and Im7.
The Im7 is an immune protein that has a high affinity with CL7(an engineered variant of colicin CE7).Through their high affinity, CL7-linker-sfGFP (another composite part we registered) can be tightly bound to InaK-linker-Im7 and the InaK in CL7-linker-sfGFP can be tightly anchored to the cell membrane, thus anchoring the entire system to the membrane surface. Finally, the InaK-linker-Im7-CL7-linker-sfGFP system is displayed on the surface of the membrane(Figure 1).Additionally, the sfGFP is a green fluorescent protein. In this system, sfGFP can be used to verify the anchoring of the system through fluorescence confocal experiments (for details, please refer to the engineering section).
After validation is completed, replacing sfGFP with targeting elements such as single-chain antibodies can achieve targeting functions. It should be noted that our designed system utilizes the high affinity of CL7 and Im7, so some components can be flexibly replaced according to needs, suitable for different usage scenarios. For example, we can replace the ice nucleation protein with different ones for different cells, and replace sfGFP with different single-chain antibodies, nanobodies, etc., according to different targeting targets.

im7-cl7.png

Figure 1. Schematic diagram of the targeting plug-in pairing system for Im7 protein to CL7 fusion pair displayed on the EcN surface.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1800
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 722
    Illegal NgoMIV site found at 962
    Illegal NgoMIV site found at 1130
    Illegal AgeI site found at 517
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 692
    Illegal BsaI.rc site found at 1182
    Illegal SapI.rc site found at 326