Team:SJTU-BioX-Shanghai/Project/Subproject2

Stop-Codon Switch

Background

The Rare Codon Modulator can only regulate the amount of target protein. 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. Peter Schultz and his co-workers 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 using

Modulator: control 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

Modulator:

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

• aaRS: the modified AspRS used in our Rare-Codon Modulator can be used here. This modified enzyme can charge Asp to tRNA^Asp-TAG.

Click here to see Modeling.

Reporter:

• Reporter for Qualitative Analysis:

GFP and RFP linked with a flexible chain. A stop codon TAG is inserted in the flexible chain.

Action: If the ribosome can get through the stop codon with the help of Modulator, both GFP and RFP can be expressed. If the ribosome cannot get through the stop codon, only GFP will be expressed.

• Reporter for Quantitative analysis:

We use luciferase as our reporter gene for quantitative analysis. A TAG codon is inserted after the initial codon of the gene.

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

The function of Switch is characterized by the amount of luciferase expressed.

The amount of luciferase expressed is reflected by the light emitted when luciferase acts on the appropriate luciferin substrate.

The light can be measured by luminometer and the quantity is positively correlated with the amount of luciferase and its activity (learn more...).

Results

Based on the design of Stop-Codon Switch, we have tested whether the modified AspRS can charge tRNA^Asp-TAG with Asp. Both qualitative and quantitative tests are carried out.

• Qualitative Test: we have designed PT7-GFP-TAG-RFP([http://partsregistry.org/wiki/index.php?title=Part:BBa_K567018 BBa_K567018]) as our reporter gene. If the Modulator: 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]) can work together properly, we can observe red fluorescence. Otherwise only green fluorescence can be observed under the UV light. Unfortunately we did not obtain the expected results in our experiments. Yet we have demonstrated in our Quantitative Test that the Stop-Codon Modulator is functional. We proposed that the amount of RFP produced may be too little to be observed in our previous test.

• Quantitative Test: we have used Pbla-Luc-TAG 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 the Modulator for Stop-Codon Switch is functional, 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.

Referance

1.Cropp, T.A. and P.G. Schultz, An expanding genetic code. Trends Genet, 2004. 20(12): p. 625-30.

2.Liu, C.C., et al., Efficient expression of tyrosine-sulfated proteins in E. coli using an expanded genetic code. Nat Protoc, 2009. 4(12): p. 1784-9.

3.Liu, C.C. and P.G. Schultz, Adding new chemistries to the genetic code. Annu Rev Biochem. 79: p. 413-44.

4.Liu, D.R., T.J. Magliery, and P.G. Schultz, Characterization of an 'orthogonal' suppressor tRNA derived from E. coli tRNA2(Gln). Chem Biol, 1997. 4(9): p. 685-91.

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.

6.Wang, F., et al., Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis. PLoS One. 5(2): p. e9354.

7.Wang, L., et al., Expanding the genetic code of Escherichia coli. Science, 2001. 292(5516): p. 498-500.

8.Wang, L. and P.G. Schultz, A general approach for the generation of orthogonal tRNAs. Chem Biol, 2001. 8(9): p. 883-90.

9.Wang, L. and P.G. Schultz, Expanding the genetic code. Chem Commun (Camb), 2002(1): p. 1-11.

10.Wang, L., J. Xie, and P.G. Schultz, Expanding the genetic code. Annu Rev Biophys Biomol Struct, 2006. 35: p. 225-49.

11.Xie, J. and P.G. Schultz, Adding amino acids to the genetic repertoire. Curr Opin Chem Biol, 2005. 9(6): p. 548-54.

12.Xie, J. and P.G. Schultz, An expanding genetic code. Methods, 2005. 36(3): p. 227-38.

13.Young, T.S. and P.G. Schultz, Beyond the canonical 20 amino acids: expanding the genetic lexicon. J Biol Chem. 285(15): p. 11039-44.

14.Zhang, Y., et al., Crystal structures of apo wild-type M. jannaschii tyrosyl-tRNA synthetase (TyrRS) and an engineered TyrRS specific for O-methyl-L-tyrosine. Protein Sci, 2005. 14(5): p. 1340-9.