Difference between revisions of "Part:BBa K3185007"

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A 3µL of protein solution dropped on PET film, then left for 20min.  Then the film was washed in TBST for 5min x3, then placed with Anti-His-tag-HRP conjugated for 1h.  ECL substrate was added, then chemiluminescence was imaged by LAS-3000.  The exposure time is 6min.
 
A 3µL of protein solution dropped on PET film, then left for 20min.  Then the film was washed in TBST for 5min x3, then placed with Anti-His-tag-HRP conjugated for 1h.  ECL substrate was added, then chemiluminescence was imaged by LAS-3000.  The exposure time is 6min.
 
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[[File:Cloth dot blot dry.png|300px|thumb|left|Fig.3a Cloth dot blot by fluorescent plastic-binding protein before washing.
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The dilution collection of each protein was dropped on PET cloth, then left for 20min.  The protein fluorescent was imaged by LAS-3000.  The exposure time is 10sec.]]
  
 
==References==
 
==References==

Revision as of 10:05, 19 October 2019


SPYCatcher -> sfGFP -> TA2

Usage and Biology

Tachystation A2(TA2) is a protein from Tachypleus tridentatus[1]. The paper shows it binds to the polystyrene (PS)[2].

We used it as the PS binding protein. We also inserted Superfolder GFP (sfGFP, BBa_I746916) which we improved GFP to make the folding time shorter in the N-terminal of LCI (BBa_I746916). By doing so, we wanted to do the binding assay with fluorescence. Moreover, we put SpyCatcher on N-terminus of sfGFP because we used the SpyTag/SpyCatcher system to bind it to other parts.

This part has four tags. First is 6×His-tag inserted in the N-terminus of SpyCatcher(BBa_K1159200) for protein purification. Second is MYC-tag inserted between sfGFP and Spy-Catcher to detect it by using the antibody. Third is a TEV protease site and we put it into two regions because it was used for protein purification in the paper[2].

We inserted it in between the BamHI site and the Ndel site on the pET11-a. We used BL21(DE3) for gene expression.We used Ni-NTA agarose for purification. After that, we confirmed the molecular weight of TA2 by using SDS-PAGE.

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
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 460

Purification


Expression

  • Cells were grown in 200ml LB media (100μg/ml Ampicillin) at 37oC shaking at 140 rpm to an OD600 of 0.5, verifying via a spectrophotometer.
  • Protein was expressed in 0.1mM IPTG for 2hours.

SDS-PAGE

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Result

Fig.Plastic-binding protein binding to PET film
A 3µL of protein solution dropped on PET film, then left for 20min. Then the film was washed in TBST for 5min x3, then placed with Anti-His-tag-HRP conjugated for 1h. ECL substrate was added, then chemiluminescence was imaged by LAS-3000. The exposure time is 6min.



Fig.3a Cloth dot blot by fluorescent plastic-binding protein before washing.
The dilution collection of each protein was dropped on PET cloth, then left for 20min. The protein fluorescent was imaged by LAS-3000. The exposure time is 10sec.

References

1 Osaki, T., Omotezako, M., Nagayama, R., Hirata, M., Iwanaga, S., Kasahara, J., Hattori, J., Ito, I., Sugiyama, H., and Kawabata, S.I. (1999).
Horseshoe crab hemocyte-derived antimicrobial polypeptides, tachystatins, with sequence similarity to spider neurotoxins.
J. Biol. Chem. 274, 26172–26178.

2 Directed evolution of polypropylene and polystyrene binding peptides
Veggiani, G., Nakamura, T., Brenner, M.D., Gayet, R. V., Yan, J., Robinson, C. V., and Howarth, M. (2016).
Programmable polyproteams built using twin peptide superglues.
Proc. Natl. Acad. Sci. U. S. A. 113, 1202–1207.