Difference between revisions of "Part:BBa K4245113:Design"

 
 
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===Design Notes===
 
===Design Notes===
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For the padlock probe  (PLP) design, part of the reverse complement of the miRNA makes up each end of the padlock probe. To determine where the reverse complement is split properly, we determined the annealing temperatures of each arm through SnapGene. To allow successful hybridization and maximize the binding efficiency of the miRNA and the padlock arms, the arms need to have the same annealing temperature. Furthermore, we added a phosphate group modification to the 5’ end of the padlock sequence to allow ligation by SplintR ligase (Jonstrup et al., 2006).
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[[File:Padlock_Probe_Arrangement_Formation.jpg|thumb|center|500px|<i>Figure 1. The arrangement of the padlock probes and their target miRNAs. </i>]]
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Additionally, the alignment of the 5’ and 3’ ends is essential to determine where each part of the padlock and its arms matches up to the target miRNA (Liu et al., 2013). The miRNA strand hybridizes antiparallel to the padlock arms (see Fig. 1) Therefore, the 5’ end of the miRNA will end up overlapping the 5’ PLP arm, and the 3’ end of the miRNA will end up overlapping the 3’ PLP arm (Liu et al., 2013).
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===Source===
 
===Source===
  
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===References===
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Jonstrup, S. P., Koch, J., & Kjems, J. (2006). A microrna detection system based on padlock probes and rolling circle amplification. RNA, 12(9), 1747–1752. https://doi.org/10.1261/rna.110706
  
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===References===
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Liu, H., Li, L., Duan, L., Wang, X., Xie, Y., Tong, L., Wang, Q., & Tang, B. (2013). High specific and ultrasensitive isothermal detection of microRNA by padlock probe-based exponential rolling circle amplification. Analytical Chemistry, 85(16), 7941–7947. https://doi.org/10.1021/ac401715k

Latest revision as of 16:55, 11 October 2022


5


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

For the padlock probe (PLP) design, part of the reverse complement of the miRNA makes up each end of the padlock probe. To determine where the reverse complement is split properly, we determined the annealing temperatures of each arm through SnapGene. To allow successful hybridization and maximize the binding efficiency of the miRNA and the padlock arms, the arms need to have the same annealing temperature. Furthermore, we added a phosphate group modification to the 5’ end of the padlock sequence to allow ligation by SplintR ligase (Jonstrup et al., 2006).

Figure 1. The arrangement of the padlock probes and their target miRNAs.


Additionally, the alignment of the 5’ and 3’ ends is essential to determine where each part of the padlock and its arms matches up to the target miRNA (Liu et al., 2013). The miRNA strand hybridizes antiparallel to the padlock arms (see Fig. 1) Therefore, the 5’ end of the miRNA will end up overlapping the 5’ PLP arm, and the 3’ end of the miRNA will end up overlapping the 3’ PLP arm (Liu et al., 2013).

Source

References

Jonstrup, S. P., Koch, J., & Kjems, J. (2006). A microrna detection system based on padlock probes and rolling circle amplification. RNA, 12(9), 1747–1752. https://doi.org/10.1261/rna.110706

Liu, H., Li, L., Duan, L., Wang, X., Xie, Y., Tong, L., Wang, Q., & Tang, B. (2013). High specific and ultrasensitive isothermal detection of microRNA by padlock probe-based exponential rolling circle amplification. Analytical Chemistry, 85(16), 7941–7947. https://doi.org/10.1021/ac401715k