Difference between revisions of "Part:BBa K4247020:Design"

 
 
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===Design Notes===
 
===Design Notes===
 
MFP151 is a long protein and as such, its sequence might be difficult to synthesise. Hence, at the UCopenhagen team, we have split the sequence into two halves such that each half of the sequence would be produced in 2 expression plasmids each. These two halves can be put together by Golden Gate Cloning to obtain the sequence coding for the full MFP151 protein.  
 
MFP151 is a long protein and as such, its sequence might be difficult to synthesise. Hence, at the UCopenhagen team, we have split the sequence into two halves such that each half of the sequence would be produced in 2 expression plasmids each. These two halves can be put together by Golden Gate Cloning to obtain the sequence coding for the full MFP151 protein.  
 +
  
 
Both halves of the sequence coding for MFP151 are contained in an pET24 (+) expression vector having a T7 promoter, terminator, KAN resistance gene and a 6x His-tag in the C-terminus of the protein.  
 
Both halves of the sequence coding for MFP151 are contained in an pET24 (+) expression vector having a T7 promoter, terminator, KAN resistance gene and a 6x His-tag in the C-terminus of the protein.  
 +
  
 
Further, this sequence was codon optimised as per E.coli's codon bias.
 
Further, this sequence was codon optimised as per E.coli's codon bias.
  
  
−
 
+
[[File:mfp151pl.png|600px|]]
  
 
===Source===
 
===Source===
  
−
The sequence of this composite part is obtained from the following basic parts: BBa_K4247018 (mfp151_first-half) and BBa_K4247019 (mfp151_second-half).
+
The sequence of this composite part is obtained from the following basic parts: <partinfo>BBa_K4247018</partinfo> (mfp151_first-half) and <partinfo>BBa_K4247019</partinfo> (mfp151_second-half).
  
 
===References===
 
===References===
 +
 +
Hwang, D. S., Gim, Y., Yoo, H. J., & Cha, H. J. (2007). Practical recombinant hybrid mussel bioadhesive fp-151. Biomaterials, 28(24), 3560–3568. https://doi.org/10.1016/j.biomaterials.2007.04.039
 +
 +
Lin, Q., Gourdon, D., Sun, C., Holten-Andersen, N., Anderson, T. H., Waite, J. H., & Israelachvili, J. N. (2007). Adhesion mechanisms of the mussel foot proteins mfp-1 and mfp-3. Proceedings of the National Academy of Sciences of the United States of America, 104(10), 3782–3786. https://doi.org/10.1073/pnas.0607852104
 +
 +
Kim, E., Dai, B., Qiao, J. B., Li, W., Fortner, J. D., & Zhang, F. (2018). Microbially Synthesized Repeats of Mussel Foot Protein Display Enhanced Underwater Adhesion. ACS applied materials & interfaces, 10(49), 43003–43012. https://doi.org/10.1021/acsami.8b14890
 +
 +
Mengkui Cui, Susu Ren, Shicao Wei, Chengjun Sun, and Chao Zhong,"Natural and bio-inspired underwater adhesives: Current progress and new perspectives", APL Materials 5, 116102 (2017) https://doi.org/10.1063/1.4985756

Latest revision as of 14:12, 10 October 2022


Mfp151


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]


Design Notes

MFP151 is a long protein and as such, its sequence might be difficult to synthesise. Hence, at the UCopenhagen team, we have split the sequence into two halves such that each half of the sequence would be produced in 2 expression plasmids each. These two halves can be put together by Golden Gate Cloning to obtain the sequence coding for the full MFP151 protein.


Both halves of the sequence coding for MFP151 are contained in an pET24 (+) expression vector having a T7 promoter, terminator, KAN resistance gene and a 6x His-tag in the C-terminus of the protein.


Further, this sequence was codon optimised as per E.coli's codon bias.


Mfp151pl.png

Source

The sequence of this composite part is obtained from the following basic parts: BBa_K4247018 (mfp151_first-half) and BBa_K4247019 (mfp151_second-half).

References

Hwang, D. S., Gim, Y., Yoo, H. J., & Cha, H. J. (2007). Practical recombinant hybrid mussel bioadhesive fp-151. Biomaterials, 28(24), 3560–3568. https://doi.org/10.1016/j.biomaterials.2007.04.039

Lin, Q., Gourdon, D., Sun, C., Holten-Andersen, N., Anderson, T. H., Waite, J. H., & Israelachvili, J. N. (2007). Adhesion mechanisms of the mussel foot proteins mfp-1 and mfp-3. Proceedings of the National Academy of Sciences of the United States of America, 104(10), 3782–3786. https://doi.org/10.1073/pnas.0607852104

Kim, E., Dai, B., Qiao, J. B., Li, W., Fortner, J. D., & Zhang, F. (2018). Microbially Synthesized Repeats of Mussel Foot Protein Display Enhanced Underwater Adhesion. ACS applied materials & interfaces, 10(49), 43003–43012. https://doi.org/10.1021/acsami.8b14890

Mengkui Cui, Susu Ren, Shicao Wei, Chengjun Sun, and Chao Zhong,"Natural and bio-inspired underwater adhesives: Current progress and new perspectives", APL Materials 5, 116102 (2017) https://doi.org/10.1063/1.4985756