Difference between revisions of "Part:BBa K3752000"
 
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cgRNA which senses the mRNA of OXA-48 - used as a riboswitch by 2021 Warwick iGEM.
 
cgRNA which senses the mRNA of OXA-48 - used as a riboswitch by 2021 Warwick iGEM.
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NUPACK modelling was used to confirm the function of this part in silico as laboratory work could not be used to verify this due to time constraints.
 +
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[[File:T--Warwick--parentunannealed.png|600px|center]]<br>
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As seen above, the natively folded state of the cgRNA does not present the dCas9 binding handle.<br>
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[[File:T--Warwick--parentannealed.png|600px|centre]]<br>
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Yet when the cgRNA anneals with the OXA-48 mRNA, the dCas9 binding handle (top in this image) is folded correctly, switching the CRISPRa system on.
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<b>Everything below is obtained through computational modelling - no wet lab verification of these data was possible due to time constraints.</b><br>
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<b>All secondary structure simulations were obtained through NUPACK. The data in all the graphs are obtained from a COPASI model, the parameters for which can be found at the bottom of our Engineering page (https://2021.igem.org/Team:Warwick/Engineering).</b>
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Below is a NUPACK simulation of the folding of this cgRNA (centre) as opposed to a cgRNA with a shorter sensing loop (left) and one with a longer sensing loop (right). All sensing loops labelled in yellow.
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[[File:T--Warwick--SML.png|600px|center]]
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The cgRNA with the shorter sensing loop fails to fold into the correct secondary structure at all, making it unable to function at all. The cgRNA with the longer loop folds correctly but the longer sensing domain reduces specificity, making cross-activation more likely.
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 +
[[File:T--Warwick--SMLG.png|600px|center]]
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Above is a simulation of the fluorescence obtained through the use of these cgRNAs; as expected, the shorter sensing loop causes no increase in fluorescence with respect to the negative control, whereas both the optimum length and long cgRNAs offer a marked increase in the expression of the fluorescent reporter.
 +
 +
[[File:T--Warwick--OptimumCentral.png|600px|center]]
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Above is a comparison of the simulated folding of the optimum cgRNA and a cgRNA with a central mismatch when compared to BBa_K3752000. The probability of the mismatching cgRNA equilibrating in the right conformation is low (20%), making its activating effect far lower than the optimum one's. The comparison in fluorescence between the two is visible below.
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[[File:T--Warwick--OptimumCentralG.png|600px|center]]
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Below is a comparison between the cgRNA with the shorter sensing loop described previously and a cgRNA with a mismatch at one of the ends of the sensing loop. Both tend to adopt similar secondary structures, which are known to be inactive - the cgRNA can therefore tolerate no mutations towards the ends of its sensing loop.
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[[File:T--Warwick--OptimumShort.png|600px|center]]
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This is verified through a simulation, the graph for which is visible below.
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[[File:T--Warwick--OptimumShortG.png|600px|center]]
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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[[File:T--Warwick--parentunannealed.png|600px|center]]
 
 
<partinfo>BBa_K3752000 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K3752000 SequenceAndFeatures</partinfo>
  

Latest revision as of 22:39, 21 October 2021


OXA-48 Parent cgRNA

cgRNA which senses the mRNA of OXA-48 - used as a riboswitch by 2021 Warwick iGEM.

NUPACK modelling was used to confirm the function of this part in silico as laboratory work could not be used to verify this due to time constraints.

T--Warwick--parentunannealed.png

As seen above, the natively folded state of the cgRNA does not present the dCas9 binding handle.

T--Warwick--parentannealed.png

Yet when the cgRNA anneals with the OXA-48 mRNA, the dCas9 binding handle (top in this image) is folded correctly, switching the CRISPRa system on.

Everything below is obtained through computational modelling - no wet lab verification of these data was possible due to time constraints.
All secondary structure simulations were obtained through NUPACK. The data in all the graphs are obtained from a COPASI model, the parameters for which can be found at the bottom of our Engineering page (https://2021.igem.org/Team:Warwick/Engineering).

Below is a NUPACK simulation of the folding of this cgRNA (centre) as opposed to a cgRNA with a shorter sensing loop (left) and one with a longer sensing loop (right). All sensing loops labelled in yellow.

T--Warwick--SML.png

The cgRNA with the shorter sensing loop fails to fold into the correct secondary structure at all, making it unable to function at all. The cgRNA with the longer loop folds correctly but the longer sensing domain reduces specificity, making cross-activation more likely.

T--Warwick--SMLG.png

Above is a simulation of the fluorescence obtained through the use of these cgRNAs; as expected, the shorter sensing loop causes no increase in fluorescence with respect to the negative control, whereas both the optimum length and long cgRNAs offer a marked increase in the expression of the fluorescent reporter.

T--Warwick--OptimumCentral.png

Above is a comparison of the simulated folding of the optimum cgRNA and a cgRNA with a central mismatch when compared to BBa_K3752000. The probability of the mismatching cgRNA equilibrating in the right conformation is low (20%), making its activating effect far lower than the optimum one's. The comparison in fluorescence between the two is visible below.

T--Warwick--OptimumCentralG.png

Below is a comparison between the cgRNA with the shorter sensing loop described previously and a cgRNA with a mismatch at one of the ends of the sensing loop. Both tend to adopt similar secondary structures, which are known to be inactive - the cgRNA can therefore tolerate no mutations towards the ends of its sensing loop.

T--Warwick--OptimumShort.png

This is verified through a simulation, the graph for which is visible below.

T--Warwick--OptimumShortG.png


Sequence and Features


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]