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From 2014.igem.org

Contents 1 Introduction 2 NpuDnaE intein RFC [???] circularization constructs 2.1 Design 2.2 Cloning 2.3 Results 3 Sortase A circularization constructs 3.1 Design 3.2 Cloning 3.3 Results? 4 References

Introduction

The most promising approaches to circularize proteins are protein trans-splicing using split inteins [1] such as Npu DnaE [2] and Sortase A-catalyzed cyclization [3]. Both methods require the addition of specific proteins domains or peptides to the protein to be circularized. Consequently, on DNA level, creating circular proteins equals creating fusion proteins. However, existing protein fusion standards like RFC 23 cause scars.

NpuDnaE intein RFC [???] circularization constructs

- Bild: 000, 001

Design

Cloning

mechanismus?

Results

Sortase A circularization constructs

- Bild: 002, 003

Design

Cloning

Results?

mechanismus?

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] 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).

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