Team:SJTU-BioX-Shanghai/Project/Subproject2

Stop-Codon Switch

Background

The Rare Codon Switch can only regulate the amount of target protein production. To make our device a strict molecular switch that turns on/off protein biosynthesis, we need to eliminate the background.

In recent years, stop codons (codon_ST) and stop codon suppressor tRNAs (tRNA_SS) are used to incorporate unnatural amino acids in protein biosynthesis. Researchers like Peter Schultz and Kiga have made a lot of contributions in this field. The advantage of codon_ST and tRNA_SS is that they can incorporate target amino acids without background noise. We make use of codon_ST and tRNA_SS as the controlling element for protein biosynthesis.

Introduction

We design a Stop-Codon Switch to turn on/off protein translation.

We can control the translation process by controlling whether the ribosome can get through the stop codon placed in the target protein's mRNA.

This process can be achieved by controlling the existence of charged tRNA_SS that recognizes the stop codon. This process is controlled by two elements:

The existence of tRNA_SS

aminoacyl tRNA synthetases (aaRS) that can charge tRNA_SS

Reporter: a stop codon is put immediately after the initial codon ATG in the target protein' s mRNA.

Design

• tRNA^Asp-TAG: tRNA^Asp-TAG with its anticodon mutated to CUA can base pair with stop codon UAG.

• aaRS: the modified AspRS without anticodon recognition domain. This modified enzyme can charge Asp to tRNA^Asp-TAG.

Click here to see Modeling.

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• Luciferase-TAG: A stop codon TAG is put immediately after the start codon ATG in the luciferase gene.

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Action: If the ribosome can get through the stop codon with the help of Stop-Codon Switch, luciferase can be expressed. Otherwise, luciferase cannot be expressed.

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Results

We have used Pbla-Luc-TAG ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567003 BBa_K567003]) as our Reporter. The amount of luciferase produced is reflected using the bioluminescence emitted during the luciferin reaction. Our results demonstrate that TAG insertion into luciferase blocks luciferase production, which was shown in the control group. In the experimental group, with the help of PT7-TDRS([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567011 BBa_K567011]) and tRNA^Asp-TAG([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567013 BBa_K567013]),luciferase was produced and bioluminescence was emitted during the luciferin reaction. These results proved that Stop-Codon Switch can turn on protein expression. Yet further work is needed to optimize the device.

Fig 1. Functional Analysis of Stop-Codon Switch. ER2566 cannot produce luciferase with Pbla-Luc-TAG ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567003 BBa_K567003]) only. When PT7-TDRS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567011 BBa_K567011]) and tRNA^Asp-TAG ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567013 BBa_K567013]) are also transformed into the cell, luciferase is produced. The results proved Stop-Codon Switch as a strict molecular switch without background noise.

Conclusions

We have successfully constructed the Stop-Codon Switch and have tested the device. Results proved Stop-Codon Switch as a strict molecular switch without background noise. tRNA^Asp-TAG recognizes stop codon TAG and can be charged with Asp by modified AspRS.

Referance

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5.Ryu, Y. and P.G. Schultz, Efficient incorporation of unnatural amino acids into proteins in Escherichia coli. Nat Methods, 2006. 3(4): p. 263-5.

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