Difference between revisions of "Part:BBa K4195077"

 
Line 1: Line 1:
 
 
__NOTOC__
 
__NOTOC__
<partinfo>BBa_K4195077 short</partinfo>
+
===Biology===
 
+
This sequence is the first part of guide designed for detection of toxin gene ''pirB''.
none
+
Ribozyme ENabled Detection of RNA (RENDR)<br/>
 
+
RENDR is a high-performing, plug-and-play RNA-sensing platform(''1''). RENDR utilizes a split variant of the ''Tetrahymena thermophila'' ribozyme by synthetically splitting it into two non-functional fragments (Fig. 1). Two fragments are each appended with designed RNA guide sequences, which can interact with the RNA input of interest. The split ribozyme is then inserted within a desired gene output. When bound with the RNA input, two transcribed split ribozyme fragments are triggered to self-splice and thus the intact transcript of the protein output will form.<br/>
<!-- Add more about the biology of this part here
+
[[T--XMU-China--GFP detection.png\400px]]<br/>
===Usage and Biology===
+
'''Fig. 1 Schematic illustration of RENDR.'''<br/>
 
+
===Usage and Design===
<!-- -->
+
The conserved region of ''pirB'' gene is set as the RNA input. The guide sequences were designed based on NUPACK prediction(''2''). Based on the model provided (Equation. 1), we calculate the free energy difference of candidate sequences at 37 °C, and select guide pair g1 and g2 with 215.36 kcal/mol and 205.86 kcal/mol (Fig. 2). The optimized ribozyme split sites are selected from the literature, and named α (split site 15) and β (split site 402)(''1'').<br/>
<span class='h3bb'>Sequence and Features</span>
+
'''Equation. 1 ln(FL/OD) ~ΔG<sub>Guide 1</sub> + ΔG<sub>Guide 2</sub> + ΔG<sub>RNA input</sub> − ΔG<sub>SC</sub>.'''<br/>
<partinfo>BBa_K4195077 SequenceAndFeatures</partinfo>
+
[[File:T--XMU-China--pirB g1α Nupack.png|400px]<br/>
 
+
'''Fig. 2 The MFE structure of g1 guide-input complex at 37℃.''' ΔG<sub>Guide1</sub> and ΔG<sub>Guide2</sub> = The minimum free energy (MFE) of the two RNA guide sequences attached to each fragment of the RENDR ribozyme. ΔG<sub>RNAinput</sub> = The MFE of the RNA input. ΔG<sub>SC</sub> = The duplex binding energy of the complex. ΔG<sub>Guide1</sub> = -13.2 kcal/mol, ΔG<sub>Guide2</sub> = -10.6 kcal/mol, ΔG<sub>RNAinpu</sub> = -27.9 kcal/mol, ΔG<sub>SC</sub> = -267.06 kcal/mol, ΔG<sub>SC</sub> - ΔG<sub>Guide1</sub> + ΔG<sub>Guide2</sub> + ΔG<sub>RNAinput</sub> = 215.36 kcal/mol.<br/>
 
+
<!-- Uncomment this to enable Functional Parameter display
+
===Functional Parameters===
+
<partinfo>BBa_K4195077 parameters</partinfo>
+
<!-- -->
+

Revision as of 13:18, 10 October 2022

Biology

This sequence is the first part of guide designed for detection of toxin gene pirB. Ribozyme ENabled Detection of RNA (RENDR)
RENDR is a high-performing, plug-and-play RNA-sensing platform(1). RENDR utilizes a split variant of the Tetrahymena thermophila ribozyme by synthetically splitting it into two non-functional fragments (Fig. 1). Two fragments are each appended with designed RNA guide sequences, which can interact with the RNA input of interest. The split ribozyme is then inserted within a desired gene output. When bound with the RNA input, two transcribed split ribozyme fragments are triggered to self-splice and thus the intact transcript of the protein output will form.
T--XMU-China--GFP detection.png\400px
Fig. 1 Schematic illustration of RENDR.

Usage and Design

The conserved region of pirB gene is set as the RNA input. The guide sequences were designed based on NUPACK prediction(2). Based on the model provided (Equation. 1), we calculate the free energy difference of candidate sequences at 37 °C, and select guide pair g1 and g2 with 215.36 kcal/mol and 205.86 kcal/mol (Fig. 2). The optimized ribozyme split sites are selected from the literature, and named α (split site 15) and β (split site 402)(1).
Equation. 1 ln(FL/OD) ~ΔGGuide 1 + ΔGGuide 2 + ΔGRNA input − ΔGSC.
[[File:T--XMU-China--pirB g1α Nupack.png|400px]
Fig. 2 The MFE structure of g1 guide-input complex at 37℃. ΔGGuide1 and ΔGGuide2 = The minimum free energy (MFE) of the two RNA guide sequences attached to each fragment of the RENDR ribozyme. ΔGRNAinput = The MFE of the RNA input. ΔGSC = The duplex binding energy of the complex. ΔGGuide1 = -13.2 kcal/mol, ΔGGuide2 = -10.6 kcal/mol, ΔGRNAinpu = -27.9 kcal/mol, ΔGSC = -267.06 kcal/mol, ΔGSC - ΔGGuide1 + ΔGGuide2 + ΔGRNAinput = 215.36 kcal/mol.