Difference between revisions of "Part:BBa K2206001"

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{{Template:CLSB-UK 17 Images 27b3p 1}}
 
{{Template:CLSB-UK 17 Images 27b3p 1}}
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===Information contributed by City of London UK (2021)===
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[[File:ToeholdTools.png|x200px|center]]
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This toehold switch was characterized <i>in silico</i> using the ToeholdTools project that our team developed.
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See https://github.com/lkn849/thtools for more information.
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Metadata:
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*'''Group:''' City of London UK 2021
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*'''Author:''' Lucas Ng
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*'''Summary:''' Used our software ToeholdTools to investigate the target miRNA specificity and activation of this part.
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Raw data:
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*[[Media:BBa_K2206001_thtest.txt]]
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*[[Media:BBa_K2206001_crt.txt]]
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This contribution was autogenerated by the script '''contrib.py''', available at https://github.com/lkn849/thtools/tree/master/registry.
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----
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This switch was designed to detect the miRNA hsa-miR-27b-3p at a temperature of 37.
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We tested it against every <i>Homo sapiens</i> RNA in miRBase and our analysis shows that it is best used to detect hsa-miR-6752-5p.
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With hsa-miR-6752-5p at 37°C, the switch has a specificity of 20 ± 100 % and an activation of 15 ± 5 %.
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These values represent 95% confidence limits (z=1.96).
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The temperature&ndash;activation&ndash;specificity relationship is shown here:
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[[File:BBa_K2206001_graph.png|500px|center]]
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Error bars represent the standard error (SE).
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The line of best fit was calculated using a univariate cubic spline weighted inverse to each point's SE.
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'''Caveats:'''
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*As per the above, we cannot confirm that this switch detects the desired RNA sequence.
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*Although at the indented usage temperature of {celsius}°C this switch best detected {inferred_target_name}, this RNA did not appear as a best target for any of separate tests taken at the temperatures tested in the above graph ({temperature_range}). Therefore, we cannot confirm the reliability of this switch.
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We do not recommend this part for future usage.
  
 
<!-- Add more about the biology of this part here
 
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Revision as of 10:26, 7 October 2021

Toehold switch for hsa-miR-27b-3p

Toehold switches are synthetic riboregulators that regulate gene expression post-transcriptionally. Gene expression can be activated in the presence of a cognate single stranded RNA molecule that contains an arbitrary sequence (the trigger RNA). The trigger RNA binds to the switch through base pairing, causing a conformational change that results in translation of the downstream protein coding region.

This part codes for a toehold switch that contains a region that is complementary to the microRNA hsa-miR-27b-3p (the trigger RNA). In the presence of hsa-miR-27b-3p, translation of the downstream protein coding region occurs.

This part can be used to regulate the expression of any protein in response to the levels of hsa-miR-27b-3p present in a system.

The transcripts produced by this part are toxic to E. coli. Therefore, we recommend the use of an inducible non-leaky promoter to allow for amplification in E. coli. For reference, we found Bba_K808000 was too leaky.

This part contains a strong RBS sequence.

NUPACK Structure Analysis

Start codonRBSTrigger Binding SiteFree energy of secondary structure: -18.80 kcal/molACGUMFE structure at 37.0°CTrigger Binding SitemiRNAStartcodonRBSFree energy of secondary structure: -46.98 kcal/molACGUMFE structure at 37.0°C

Information contributed by City of London UK (2021)

ToeholdTools.png

This toehold switch was characterized in silico using the ToeholdTools project that our team developed. See https://github.com/lkn849/thtools for more information.

Metadata:

  • Group: City of London UK 2021
  • Author: Lucas Ng
  • Summary: Used our software ToeholdTools to investigate the target miRNA specificity and activation of this part.

Raw data:

This contribution was autogenerated by the script contrib.py, available at https://github.com/lkn849/thtools/tree/master/registry.


This switch was designed to detect the miRNA hsa-miR-27b-3p at a temperature of 37. We tested it against every Homo sapiens RNA in miRBase and our analysis shows that it is best used to detect hsa-miR-6752-5p.

With hsa-miR-6752-5p at 37°C, the switch has a specificity of 20 ± 100 % and an activation of 15 ± 5 %. These values represent 95% confidence limits (z=1.96).

The temperature–activation–specificity relationship is shown here:

BBa K2206001 graph.png

Error bars represent the standard error (SE). The line of best fit was calculated using a univariate cubic spline weighted inverse to each point's SE.

Caveats:

  • As per the above, we cannot confirm that this switch detects the desired RNA sequence.
  • Although at the indented usage temperature of {celsius}°C this switch best detected {inferred_target_name}, this RNA did not appear as a best target for any of separate tests taken at the temperatures tested in the above graph ({temperature_range}). Therefore, we cannot confirm the reliability of this switch.

We do not recommend this part for future usage.

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]