Difference between revisions of "Part:BBa K3185007"
0012massan (Talk | contribs) |
0012massan (Talk | contribs) |
||
Line 3: | Line 3: | ||
<partinfo>BBa_K3185007 short</partinfo> | <partinfo>BBa_K3185007 short</partinfo> | ||
==Usage and Biology== | ==Usage and Biology== | ||
− | Tachystation A2(TA2) is a protein from <i>Tachypleus tridentatus</i>[1]. The paper | + | Tachystation A2(TA2) is a protein from <i>Tachypleus tridentatus</i>[1]. The paper shows it binds to the polystyrene (PS)[2]. |
<br> | <br> | ||
<br> | <br> | ||
− | We used it as the PS binding protein. We also inserted Superfolder GFP (sfGFP) which we improved GFP to make the folding time shorter in the N-terminal of LCI ( | + | We used it as the PS binding protein. We also inserted Superfolder GFP (sfGFP) which we improved GFP to make the folding time shorter in the N-terminal of LCI (''<partinfo>BBa_1746916</partinfo>''). 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. | Moreover, we put SpyCatcher on N-terminus of sfGFP because we used the SpyTag/SpyCatcher system to bind it to other parts. | ||
<br> | <br> |
Revision as of 11:39, 18 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) which we improved GFP to make the folding time shorter in the N-terminal of LCI (No part name specified with partinfo tag.). 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 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
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE 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
References
[1]Horseshoe Crab Hemocyte-derived Antimicrobial Polypeptides, Tachystatins, with Sequence Similarity to Spider Neurotoxins
[2]Directed evolution of polypropylene and polystyrene binding peptides/Programmable polyproteams built using twin peptide superglues