Part:BBa_K3308009
[NrdJ-1 C (1-4)]-[Tvo VMA C48 N]
C1-construct
Overview
The Pittsburgh iGEM team 2019 designed a modular protein circuit system consisting of split Intein-based logic gates. This composite part is an input of the proposed nested intein system. This system is composed of two-independent splicing events reconstituting function functional half of a nested intein. Each nested intein’s chain (N and C terminus) will be split at one location by another split intein rendering it nonfunctional. Consequently only splicing of the “inner inteins”, will reconstruct the functional intein that is fused to the desired extein. [5]In this system, the primary splicing events taking place at each split site of the nested intein halves, will serve an AND gate. Each AND is composed of two inputs, the N- and C- terminals of matching inteins.[1]Design
This construct has the N terminus of TvoVMA Intein, it is covalently attached to the first half of the C-terminal NrdJ-1 InteinBBa_K3308070. The main purpose of this construct is to preserve functional splicing of TvoVma N intein.[1]
For TvoVMA we thought that it could better handle a C+2 change better than a N-1 change; therefore the TvoVMA was chosen to be put in this specific split site because the N and C flanking sequences on either side of the spliting site of NrdJ-1 C match what we expect is needed for efficient splicing.[3].
This construct was predicted to splice in the presence of its partner, BBa_K3308010, to form fully fucntional C-terminus NrdJ-1 (BBa_K3308012). If splicing occurs as planned between these two constructs then, addition of BBa_K3308009, BBa_K3308010, and BBa_K3308011 should result in the effective reconstruction of the full extein (GB1-GTNPC-SEIVL-gpD)- BBa_K3308013
Usage
Each construct of the set was labeled with 6XHis tag, for the purposes of purification via Ni-NTA resin(1ul/mL of culture). Following the His-tag the composite part also consists of a Tev7 Protease binding site, indicated the three dashed lines. It is important to note that the addition of the tag and cleavage site was not expected to have any impact on the splicing mechanisms of the intein.
This construct was induced and expected to react with BBa_K3308010 C2 to form the spliced product, the full terminus of the N- NrdJ-1 Intein CSP BBa_K3308012.
Results
Because this part was only the first few amino acids of the NrdJ-1 C terminal (due to the fact that we chose a split site that was closer to the N terminus of the C- Intein NrdJ-1), the construct did not as much of an issue purifying.
There was clear band in the elution which matched the expected kDa size of the contruct. The elution from the purification step was then dialyzed into a splicing buffer in which splicing reactions could be performed. The results of diafiltration are seen in the last two lanes of Figure 3. The band density decreases, however, this was enough for us to see splicing reaction with it's compliment. Because the compliment of the TvoVMA intein was hard to purify without the presence of maltose binding protein, we decided to combine this composite part and BBa_K3308084. This reaction was were promising because we deducted that there was splicing between the TvoVma inteins when both constructs had MBP. The results of this splicing reaction will be posted in our notebook page. We have also tried to combine this construct with the TvoVMA
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 116
- 1000COMPATIBLE WITH RFC[1000]
References
[1] Gramespacher, J. A., Stevens, A. J., Thompson, R. E., & Muir, T. W. (2018). Improved protein splicing using embedded split inteins. Protein Science, 27(3), 614–619. https://doi.org/10.1002/pro.3357
[2] Beyer, H.M., Mikula, K.M., Li, M.,Wlodawer, A., Iwai, H., (2019) The crystal structure of the naturally split gp41-1 intein guides the engineering of orthogonal split inteins from a cis-splicing intein.BioRxiv. https://doi.org/10.1101/546465
[3] Lockless, S. W., & Muir, T. W. (2009). Traceless protein splicing utilizing evolved split inteins. Proceedings of the National Academy of Sciences of the United States of America, 106(27), 10999–11004. https://doi.org/10.1073/pnas.0902964106
[4]  Amitai, G., Callahan, B. P., Stanger, M. J., Belfort, G., & Belfort, M. (2009). Modulation of intein activity by its neighboring extein substrates. Proceedings of the National Academy of Sciences, 106(27), 11005–11010. https://doi.org/10.1073/pnas.0904366106
[5]  Appleby-Tagoe, J. H., Thiel, I. V., Wang, Y., Wang, Y., Mootz, H. D., & Liu, X. Q. (2011). Highly efficient and more general cis- and trans-splicing inteins through sequential directed evolution. Journal of Biological Chemistry, 286(39), 34440–34447. https://doi.org/10.1074/jbc.M111.277350
[6] Shah, N. H., Eryilmaz, E., Cowburn, D., & Muir, T. W. (2013). Naturally split inteins assemble through a “capture and collapse” mechanism. Journal of the American Chemical Society, 135(49), 18673–18681. https://doi.org/10.1021/ja4104364
[7] Øemig, J. S. (2013)Structural Studies on Intein. (Published Doctoral Dissertation). University of Helsinki. Helsinki, Finland Retrieved from https://pdfs.semanticscholar.org/3c6a/b9fa31488316df5f421869163101ba13037e.pdf
Contribution Markup
This page was was last updated by Pittsburgh 2019 team.
This part is this set of nested Inteins constructs: BBa_K3308007. BBa_K3308008. BBa_K3308010. BBa_K3308011. BBa_K3308012. BBa_K3308013.
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