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From 2014.igem.org

Contents 1 Introduction 2 NpuDnaE intein RFC [i] circularization constructs 2.1 Design 2.2 Usage 3 Sortase A circularization constructs 3.1 Design 3.2 Usage 4 References

Introduction

The most promising approaches to circularize proteins are protein trans-splicing using split inteins [1] and Sortase A-catalyzed cyclization [2]. Both methods require the addition of specific proteins domains or peptides to the protein to be circularized. Consequently, on DNA level, creating circular proteins is equivalent to creating fusion proteins. However, existing protein fusion standards like [http://parts.igem.org/Help:Standards/Assembly/RFC23 RFC[23]] cause scars. Those scars on protein level may affect protein function and further complicate 3D-structure modeling. Therefore, we decided to create the new RFC[i] that allows scarless cloning of inteins. Our intein circularization constructs apply to this standard, while our sortase constructs are closely related and can be used similarly. Detailed instructions on how to use our constructs are provided in our Toolbox Guide.

NpuDnaE intein RFC [i] circularization constructs

Design

Between the coding sequences of the Npu DnaE C-intein and the N-intein we placed [http://parts.igem.org/Part:BBa_J04450 BBa_J04450], an mRFP selection marker flanked by BsaI sites that can be replaced by the protein to be circularized. A strong RBS [http://parts.igem.org/Part:BBa_K1362090 (BBa_K1362090)] was added. A version containing Smt3 was created for use with proteins that are difficult to express. [http://parts.igem.org/Part:BBa_K1362000 BBa_K1362000] was assembled by [ref to mat/met CPEC] from PCR products of [ref to pSBX1K3], [http://parts.igem.org/Part:BBa_J04450 BBa_J04450], pVS07 and pVS41 [3]. [http://parts.igem.org/Part:BBa_K1362001 BBa_K1362001] was assembled by CPEC from PCR products of [http://parts.igem.org/Part:BBa_K1362000 BBa_K1362000] and pRSFDuet-1-mDNMT1(731-1602) [4].

Usage

Exteins, RFC [i] standard overhangs and BsaI sites have to be added to the coding sequence of the protein to be circularized without start- and stop codons by PCR. By Golden Gate assembly, the mRFP selection marker has to be replaced with the protein insert. After addition of an inducible promotor the circular protein is ready to be expressed. For detailed step-by-step instructions please use our Toolbox Guide.

Upon expression of the fusion protein, the split intein domains reassemble to the active intein and thus ligate the termini of the protein to be circularized in trans-splicing reaction.

These constructs were successfully used to circularize lambda lysozyme and xylanase and probably DNMT1.

Sortase A circularization constructs

Design

The mRFP selection marker [http://parts.igem.org/Part:BBa_J04450 BBa_J04450], which can be removed by restriction with BsaI, is flanked by TEV protease cleavage site (left) and a sorting signal (right) with a His6 tag. By Golden gate assembly, the selection marker can be replaced by the protein to be circularized. A version containing Smt3 and a FLAG tagwas created for use with proteins that are difficult to express. The constructs [http://parts.igem.org/Part:BBa_K1362202 BBa_K1362202] and [http://parts.igem.org/Part:BBa_K1362003 BBa_K1362003] were assembled in a row of CPEC and biobrick cloning steps from the following sources [http://parts.igem.org/Part:pSB1A3 pSB1A3], [http://parts.igem.org/Part:BBa_K1362093 BBa_K1362093], [http://parts.igem.org/Part:BBa_J04450 BBa_J04450], pDONR and pRSFDuet-1-mDNMT1(731-1602) [4]. Please use our notebook for detailed information.

Usage

BsaI sites and overhangs as in figure 6 have to be added to the coding sequence of the protein to be circularized without start- and stop codons by PCR. By Golden Gate assembly, the mRFP selection marker has to be replaced with the protein insert. After addition of an inducible promotor protein is ready to be expressed. The protein has to be purified and treated with TEV protease and sortase A. The sortase A catalyzes the transpeptidation reaction that leads to backbone circularization. For detailed step-by-step instructions please use our Toolbox Guide.

References

[1] Iwai, H., Lingel, a & Pluckthun, a. Cyclic green fluorescent protein produced in vivo using an artificially split PI-PfuI intein from Pyrococcus furiosus. J. Biol. Chem. 276, 16548–54 (2001).

[2] Antos, J. M. et al. A straight path to circular proteins. J. Biol. Chem. 284, 16028–36 (2009).

[3] Zettler, J., Schütz, V. & Mootz, H. D. The naturally split Npu DnaE intein exhibits an extraordinarily high rate in the protein trans-splicing reaction. FEBS Lett. 583, 909–14 (2009).

[4] Song, J., Rechkoblit, O., Bestor, T. H. & Patel, D. J. Structure of DNMT1-DNA complex reveals a role for autoinhibition in maintenance DNA methylation. Science 331, 1036–40 (2011).