Difference between revisions of "Part:BBa K4207026"
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+ | <b>Figure 1</b>. Toehold switch mechanism. This animation illustrates the operation of the toehold switch. Initially, the structure is in an inactive state and the RBS and the start codon are hidden in the stem-loop. When a specific trigger binds to the binding site, the stem-loop structure opens and the ribosome binding site and start codon are revealed. | ||
+ | |||
</div> | </div> | ||
</center> | </center> | ||
</html> | </html> | ||
+ | |||
+ | To use this toehold switch, it should be assembled in a construct containing a promoter, the toehold switch, a protein-coding sequence, and optionally a terminator if the sensor is not to be used as linear. To prevent frame-shifting, the toehold switch should be combined with the coding sequence using scarless assembly. | ||
<!-- --> | <!-- --> | ||
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===2. Design=== | ===2. Design=== | ||
+ | |||
+ | This toehold switch was designed according to the A-series ideal structure from Pardee et al. (2016). This structure was improved from the original toehold switch structure (Green et al., 2014) to reduce translational leakage. We screened the Potato Virus Y genome for conserved sequences. Each sequence was divided into 36-nucleotide long subsequences and we designed toehold switches designed to specifically bind to the sequence. This toehold switch was designed using the 21-nucleotide linker (Green et al., 2014). We assigned a score for each toehold switch based on the three-parameter fit from Ma et al. (2018) and selected the best-ranking toehold switches for our library. | ||
===3. Characterization=== | ===3. Characterization=== | ||
− | <gallery caption=" | + | Score predicted by our model: |
− | File:PVY_A1_inactive.png|Structure of inactive form | + | <gallery caption="" widths="400px" heights="400px" perrow="6"> |
− | File:PVY_A1_active.png|Structure of active form | + | File:PVY_A1_inactive.png|<b>Figure 2.</b> Structure of inactive form. The picture was created with the NUPACK web app (Zadeh et al., 2010) |
+ | File:PVY_A1_active.png|<b>Figure 3.</b> Structure of active form. The picture was created with the NUPACK web app (Zadeh et al., 2011) | ||
</gallery> | </gallery> | ||
+ | |||
+ | The expected structures for inactive and active toehold switches were modeled by using NUPACK’s analysis tool (Zadeh et al., 2011). This toehold switches structure closely resembles the ideal inactive and active structures. | ||
===4. Conclusion=== | ===4. Conclusion=== | ||
+ | |||
+ | Based on the data provided by our model as well as the visualization of the structures, this toehold switch is expected to exhibit trigger-dependent translation. This toehold is likely to be effective at sensing a conserved sequence in Potato Virus Y genome. However, verifying the functionality is necessary to create a viable toehold sensor construct. | ||
===5. References=== | ===5. References=== | ||
+ | |||
+ | Green, A. A., Kim, J., Ma, D., Silver, P. A., Collins, J. J., & Yin, P. (2017). Complex cellular logic computation using ribocomputing devices. Nature, 548(7665), 117–121. https://doi.org/10.1038/nature23271 | ||
+ | |||
+ | Green, A., Silver, P., Collins, J., & Yin, P. (2014). Toehold Switches: De-Novo-Designed Regulators of Gene Expression. Cell, 159(4), 925–939. https://doi.org/10.1016/j.cell.2014.10.002 | ||
+ | |||
+ | Fornace, M. E., Porubsky, N. J., & Pierce, N. A. (2020). A Unified Dynamic Programming Framework for the Analysis of Interacting Nucleic Acid Strands: Enhanced Models, Scalability, and Speed. ACS Synthetic Biology, 9(10), 2665–2678. https://doi.org/10.1021/acssynbio.9b00523 | ||
+ | |||
+ | Ma, D., Shen, L., Wu, K., Diehnelt, C. W., & Green, A. A. (2018). Low-cost detection of norovirus using paper-based cell-free systems and synbody-based viral enrichment. Synthetic Biology, 3(1). https://doi.org/10.1093/synbio/ysy018 | ||
+ | |||
+ | Pardee, K., Green, A. A., Takahashi, M. K., Braff, D., Lambert, G., Lee, J. W., Ferrante, T., Ma, D., Donghia, N., Fan, M., Daringer, N. M., Bosch, I., Dudley, D. M., O’Connor, D. H., Gehrke, L., & Collins, J. J. (2016). Rapid, Low-Cost Detection of Zika Virus Using Programmable Biomolecular Components. Cell, 165(5), 1255–1266. https://doi.org/10.1016/j.cell.2016.04.059 | ||
+ | |||
+ | Zadeh, J. N., Steenberg, C. D., Bois, J. S., Wolfe, B. R., Pierce, M. B., Khan, A. R., Dirks, R. M., & Pierce, N. A. (2010, November 17). NUPACK: Analysis and design of nucleic acid systems. Journal of Computational Chemistry, 32(1), 170–173. https://doi.org/10.1002/jcc.21596 | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 18:37, 9 October 2022
PVY toehold switch A1
1. Usage and Biology
Toehold switches are engineered riboregulators that control the expression of a downstream protein coding sequence. They can be designed to detect virtually any sequence. Toehold switches are designed in silico so that they fold into a pre-determined secondary structure. This structure contains a stable stem-loop that sequesters the ribosome binding site (RBS) and the start codon, thus preventing translation. After a specific trigger RNA binds to the binding site of the toehold, the lower part of the stem-loop unfolds, revealing the start codon. A weak stem remains, but this structure unfolds upon ribosome binding to the RBS, starting translation (Green et al., 2017). This toehold switch was designed to detect conserved sequences in the Potato Virus Y genome. The structural change of the toehold switch is illustrated in Figure 1.
To use this toehold switch, it should be assembled in a construct containing a promoter, the toehold switch, a protein-coding sequence, and optionally a terminator if the sensor is not to be used as linear. To prevent frame-shifting, the toehold switch should be combined with the coding sequence using scarless assembly.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
2. Design
This toehold switch was designed according to the A-series ideal structure from Pardee et al. (2016). This structure was improved from the original toehold switch structure (Green et al., 2014) to reduce translational leakage. We screened the Potato Virus Y genome for conserved sequences. Each sequence was divided into 36-nucleotide long subsequences and we designed toehold switches designed to specifically bind to the sequence. This toehold switch was designed using the 21-nucleotide linker (Green et al., 2014). We assigned a score for each toehold switch based on the three-parameter fit from Ma et al. (2018) and selected the best-ranking toehold switches for our library.
3. Characterization
Score predicted by our model:
The expected structures for inactive and active toehold switches were modeled by using NUPACK’s analysis tool (Zadeh et al., 2011). This toehold switches structure closely resembles the ideal inactive and active structures.
4. Conclusion
Based on the data provided by our model as well as the visualization of the structures, this toehold switch is expected to exhibit trigger-dependent translation. This toehold is likely to be effective at sensing a conserved sequence in Potato Virus Y genome. However, verifying the functionality is necessary to create a viable toehold sensor construct.
5. References
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Green, A., Silver, P., Collins, J., & Yin, P. (2014). Toehold Switches: De-Novo-Designed Regulators of Gene Expression. Cell, 159(4), 925–939. https://doi.org/10.1016/j.cell.2014.10.002
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