Team:EPF-Lausanne/Our Project/TetR mutants/MITOMI data

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{{:Team:EPF-Lausanne/Templates/TetRtemplate|title=MITOMI Data}}
{{:Team:EPF-Lausanne/Templates/TetRtemplate|title=MITOMI Data}}
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 +
<html> To find out more about the MITOMI method of characterization, please click <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">here.</a> </html>
<html> To find out more about the MITOMI method of characterization, please click <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">here.</a> </html>
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<html>The raw data from the successful experiments can be found <a href="https://2011.igem.org/File:EPFL2011_TetR_wt%26mu_raw_data.xls"> here. </a></html>
<html>The raw data from the successful experiments can be found <a href="https://2011.igem.org/File:EPFL2011_TetR_wt%26mu_raw_data.xls"> here. </a></html>
<p></p>
<p></p>
-
 
=Wildtype TetR=
=Wildtype TetR=
-
<html> <a href= >Row data</a></html>
+
===In Vitro Characterization===
 +
 
 +
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">MITOMI</a></html> technique we determined the DNA binding landscape of the wild type TetR. To do so, we first designed and generated the library of double-stranded DNA sequences that cover all possible single base substitutions within the TetO operator sequence. Based on that library we measured the dissociation constants of the mutant to all the tetO-like sequences of the library. Then, we determined the specificity of the mutant to the Tet operator sequence, expressed as a position-weight matrix (PWM).
 +
 
 +
The enoLOGO we obtained for the wild-type is:
 +
 
 +
[[File:EPFL2011_WTTetR_WebLogo.png|700px]]
 +
 
 +
 
 +
'''enoLOGO reference:'''<p>
 +
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
 +
enoLOGOS: a versatile web tool for energy normalized sequence logos.
 +
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
 +
 
 +
===Position Weight Matrix===
 +
 
 +
{| {{table}}
 +
| align="center" style="background:#f0f0f0;"|'''PO'''
 +
| align="center" style="background:#f0f0f0;"|'''A'''
 +
| align="center" style="background:#f0f0f0;"|'''T'''
 +
| align="center" style="background:#f0f0f0;"|'''C'''
 +
| align="center" style="background:#f0f0f0;"|'''G'''
 +
|-
 +
| 1||0.164072||0.519334||-0.0468541||0.22966
 +
|-
 +
| 2||0.642569||0.164072||0.188965||0.943314
 +
|-
 +
| 3||1.04481||0.558693||0.164072||0.848264
 +
|-
 +
| 4||0.959646||0.164072||2.17536||0.718959
 +
|-
 +
| 5||0.164072||1.19894||1.79469||1.56685
 +
|-
 +
| 6||1.46463||0.164072||1.74384||1.54845
 +
|-
 +
| 7||0.966397||1.07557||0.164072||1.72883
 +
|-
 +
| 8||0.164072||0.504312||0.755195||0.148902
 +
|-
 +
| 9||0.0876645||0.164072||0||0.0156484
 +
|-
 +
| 10||0.289722||0.164072||0.00707563||0.843474
 +
|-
 +
| 11||1.77568||1.3447||2.34804||0.164072
 +
|-
 +
| 12||0.164072||1.72354||1.62782||1.49176
 +
|-
 +
| 13||0.877518||0.164072||1.30879||1.9052
 +
|-
 +
| 14||0.164072||0.544642||0.3387||1.7537
 +
|-
 +
| 15||0.540091||0.8821||1.0861||0.164072
 +
|-
 +
| 16||-0.224147||0.280358||0.442769||0.164072
 +
|-
 +
| 17||0.31238||-0.0651059||0.164072||-0.303844
 +
|}
 +
 
 +
Each row represents the changes in binding energy,  ΔΔG (kcal/mol), compared to the reference sequence upon the substitution of the indicated nucleotide at a certain position within the target DNA element. Values are indicated in kcal/mol.
=Mutant TetRs=
=Mutant TetRs=
Line 16: Line 75:
<html> <a href=http://partsregistry.org/Part:BBa_K613013>BBa_K613013</a></html>
<html> <a href=http://partsregistry.org/Part:BBa_K613013>BBa_K613013</a></html>
-
===In vitro characterization===
+
===In Vitro Characterization===
-
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Our_Project/TetR_mutants/MITOMI_data">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR V36F mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM).
+
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR V36F mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM).
-
WebLogo we obtained for the V36F mutant:
+
The enoLOGO we obtained for the V36F mutant:
[[File:EPFL2011_MITOMI_WebLogo_V36F.png|700px]]
[[File:EPFL2011_MITOMI_WebLogo_V36F.png|700px]]
-
'''Reference:'''<p>
+
'''enoLOGO reference:'''<p>
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
enoLOGOS: a versatile web tool for energy normalized sequence logos.
enoLOGOS: a versatile web tool for energy normalized sequence logos.
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
-
 
-
 
===Position Weight Matrix===
===Position Weight Matrix===
Line 78: Line 135:
Each row represents the changes in binding energy,  ΔΔG (kcal/mol), compared to the reference sequence upon the substitution to the indicated nucleotide at certain position within the target DNA element. Values are indicated in kcal/mol.
Each row represents the changes in binding energy,  ΔΔG (kcal/mol), compared to the reference sequence upon the substitution to the indicated nucleotide at certain position within the target DNA element. Values are indicated in kcal/mol.
-
We compared the measured DNA binding affinities of the V36F mutant to the affinities obtained for the  wt-TetR and found that V36F mutant interacts with the tetO as strong as the wild-type variant.
+
We compared the measured DNA binding affinities of the V36F mutant to the affinities obtained for the  wt-TetR and found that V36F mutant interacts with the TetO as strongly as the wild-type variant.
[[File:EPFL2011_Scatter_plot_kd_wt_VF36.png|600px]]
[[File:EPFL2011_Scatter_plot_kd_wt_VF36.png|600px]]
-
 
-
==V36F W43S==
 
-
<html> <a href=http://partsregistry.org/Part:BBa_K613014>BBa_K613014</a></html>
 
-
 
==E37A W43S T141A==
==E37A W43S T141A==
<html> <a href=http://partsregistry.org/Part:BBa_K613015>BBa_K613015</a></html>
<html> <a href=http://partsregistry.org/Part:BBa_K613015>BBa_K613015</a></html>
-
===In vitro characterization===
+
===In Vitro Characterization===
-
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Our_Project/TetR_mutants/MITOMI_data">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR E37A  W43S T141A  mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM).
+
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR E37A  W43S T141A  mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM).  
-
WebLogo we obtained for the E37A W43S T141A mutant:
+
The measured DNA binding affinities of the E37A W43S T141A mutant show that these mutations alter the sequence recognition, while the symmetry and the spacer affinities are conserved.
 +
 
 +
 
 +
The enoLOGO we obtained for the E37A W43S T141A mutant:
[[File:EPFL2011_WebLogo_EA37WS43TA41.png|700px]]
[[File:EPFL2011_WebLogo_EA37WS43TA41.png|700px]]
-
'''Reference:'''<p>
+
'''enoLOGO reference:'''<p>
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
enoLOGOS: a versatile web tool for energy normalized sequence logos.
enoLOGOS: a versatile web tool for energy normalized sequence logos.
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
-
 
===Position Weight Matrix===
===Position Weight Matrix===
Line 152: Line 207:
<html> <a href=http://partsregistry.org/Part:BBa_K613016>BBa_K613016</a></html>
<html> <a href=http://partsregistry.org/Part:BBa_K613016>BBa_K613016</a></html>
-
===In vitro characterization===
+
===In Vitro Characterization===
-
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Our_Project/TetR_mutants/MITOMI_data">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR V36F mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM).
+
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR P39K mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM).
-
WebLogo we obtained for the P39K mutant:
+
 
 +
The enoLOGO we obtained for the P39K mutant:
[[File:EPFL2011_P39K_WebLogo.png|700px]]
[[File:EPFL2011_P39K_WebLogo.png|700px]]
 +
 +
The strong difference of the binding affinities between the P39K mutant and the wtTetR, might be due to the altered recognition of the P39K. This mutant was shown to have  a new recognition specificity for the tetO-4C operator in [http://www.sciencedirect.com/science/article/pii/S0022283697915400 Helbl et al, 1998]. 
Line 165: Line 223:
enoLOGOS: a versatile web tool for energy normalized sequence logos.
enoLOGOS: a versatile web tool for energy normalized sequence logos.
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
 +
Helbl, V., and Hillen, W. (1998). Stepwise selection of TetR variants recognizing tet operator 4C with high affinity and specificity. J Mol Biol 276, 313-318.
 +
 +
===Position Weight Matrix===
===Position Weight Matrix===
Line 216: Line 277:
<html> <a href=http://partsregistry.org/Part:BBa_K613017>BBa_K613017</a></html>
<html> <a href=http://partsregistry.org/Part:BBa_K613017>BBa_K613017</a></html>
-
==Y42F K108E==
+
===In Vitro Characterization===
-
<html> <a href=http://partsregistry.org/Part:BBa_K613018>BBa_K613018</a></html>
+
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR Y42F mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM). For the Y42F mutant we observed the decrease of the specificity compared to the wild-type tetR sequence.
 +
 
 +
The enoLOGO we obtained for the Y42F mutant:
 +
 
 +
[[File:EPFL2011_WebLogo_Y42F.png|700px]]
 +
 
 +
 
 +
The measured binding affinities show no symmetry conservation and the contribution of the outer bases equals that of the inner.  These experiment will have to be repeated in order to get a clearer idea of the binding affinities.
 +
 
 +
 
 +
'''enoLOGO reference:'''<p>
 +
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
 +
enoLOGOS: a versatile web tool for energy normalized sequence logos.
 +
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
 +
 
 +
===Position Weight Matrix===
 +
{| {{table}}
 +
| align="center" style="background:#f0f0f0;"|'''PO'''
 +
| align="center" style="background:#f0f0f0;"|'''A'''
 +
| align="center" style="background:#f0f0f0;"|'''T'''
 +
| align="center" style="background:#f0f0f0;"|'''C'''
 +
| align="center" style="background:#f0f0f0;"|'''G'''
 +
|-
 +
| 1||0.385241||0.85619||0||0.693793
 +
|-
 +
| 2||1.30965||0.385241||0.629213||1.2542
 +
|-
 +
| 3||1.18851||1.22909||0.385241||1.09825
 +
|-
 +
| 4||1.1084||0.385241||1.57045||1.20206
 +
|-
 +
| 5||0.385241||1.3955||1.10171||1.2069
 +
|-
 +
| 6||1.80251||0.385241||1.37974||1.23728
 +
|-
 +
| 7||1.25285||1.54821||0.385241||1.43937
 +
|-
 +
| 8||0.385241||0.475161||0.93954||0.488479
 +
|-
 +
| 9||0.341937||0.385241||0||0.053757
 +
|-
 +
| 10||0.973293||0.385241||0.426141||1.06563
 +
|-
 +
| 11||1.1587||1.50073||1.5542||0.385241
 +
|-
 +
| 12||0.385241||1.30762||1.11351||1.39762
 +
|-
 +
| 13||1.23638||0.385241||1.11282||1.24361
 +
|-
 +
| 14||0.385241||1.09074||0.75983||0.933921
 +
|-
 +
| 15||0.679315||1.33124||1.09937||0.385241
 +
|-
 +
| 16||0||0.467396||1.08277||0.385241
 +
|-
 +
| 17||0.664957||0.130021||0.385241||0
 +
 
 +
|}
 +
 
 +
Each row represents the changes in binding energy,  ΔΔG, compared to the reference sequence upon the substitution at the indicated nucleotide at a certain position within the target DNA element. Values are indicated in kcal/mol.
==P39Q Y42M==
==P39Q Y42M==
<html> <a href=http://partsregistry.org/Part:BBa_K613019>BBa_K613019</a></html>
<html> <a href=http://partsregistry.org/Part:BBa_K613019>BBa_K613019</a></html>
 +
===In Vitro Characterization===
 +
 +
Using the <html> <a href="https://2011.igem.org/Team:EPF-Lausanne/Tools/MITOMI">MITOMI</a></html> technique we determined the DNA binding landscape of the TetR P39Q Y42M mutant. To do so, first we designed and generated the library of double stranded DNA sequences that cover all possible single base substitution within the tetO operator sequence. Based on that library we measured the dissociation constants of the mutant to variable tetO-like sequences and determined the specificity of the mutant to the tet operator sequence (expressed as a PWM). For the P39Q Y42M mutant we observed the decrease of the specificity compared to the wild-type tetR sequence.
 +
 +
The enoLOGO we obtained for the P39Q Y42M mutant:
 +
 +
[[File:EPFL2011_P39QY42M_WebLogo.png|700px]]
 +
 +
'''enoLOGO reference:'''<p>
 +
Workman CT, Yin Y, Corcoran DL, Ideker T, Stormo GD, Benos PV.
 +
enoLOGOS: a versatile web tool for energy normalized sequence logos.
 +
Nucleic Acids Res. 2005 Jul 1;33:W389-92.</p>
 +
 +
===Position Weight Matrix===
 +
 +
{| {{table}}
 +
| align="center" style="background:#f0f0f0;"|'''PO'''
 +
| align="center" style="background:#f0f0f0;"|'''A'''
 +
| align="center" style="background:#f0f0f0;"|'''T'''
 +
| align="center" style="background:#f0f0f0;"|'''C'''
 +
| align="center" style="background:#f0f0f0;"|'''G'''
 +
|-
 +
| 1||0.455977||0.0513378||0.0469535||0.0942038
 +
|-
 +
| 2||0||0.455977||0.0808971||0.0550434
 +
|-
 +
| 3||0.024486||0||0.455977||0
 +
|-
 +
| 4||0||0.455977||0||0.175581
 +
|-
 +
| 5||0.455977||0||0.0549319||0
 +
|-
 +
| 6||0.162363||0.455977||0.0897636||0.0689181
 +
|-
 +
| 7||0||0.02975||0.455977||0.0170034
 +
|-
 +
| 8||0.455977||0||0||0.0975597
 +
|-
 +
| 9||0.134079||0.455977||0||0
 +
|-
 +
| 10||0.486152||0.455977||0.0220095||0
 +
|-
 +
| 11||0||0.0246322||0.0847586||0.455977
 +
|-
 +
| 12||0.455977||0||0||0.0321177
 +
|-
 +
| 13||0.20916||0.455977||0||0.0482279
 +
|-
 +
| 14||0.455977||0||0.0837475||0.141681
 +
|-
 +
| 15||0||0.107215||0||0.455977
 +
|-
 +
| 16||0||0||0.269667||0.455977
 +
|-
 +
| 17||0.0634094||0||0.455977||0.0582705
 +
|}
 +
 +
 +
 +
Each row represents the changes in binding energy,  ΔΔG, compared to the reference sequence upon the substitution to the indicated nucleotide at certain position within the target DNA element. Values are indicated in kcal/mol.
 +
 +
=Uncharacterized Mutant TetRs=
 +
 +
 +
Unfortunately we did not have time to finish the characterization of the following parts:
 +
 +
==Y42F K108E==
 +
 +
<html> <a href=http://partsregistry.org/Part:BBa_K613018>BBa_K613018</a></html>
 +
 +
==V36F W43S==
 +
<html> <a href=http://partsregistry.org/Part:BBa_K613014>BBa_K613014</a></html>
==P39Q Y42M L197S==
==P39Q Y42M L197S==

Latest revision as of 21:49, 26 October 2011

Retrieved from "http://2011.igem.org/Team:EPF-Lausanne/Our_Project/TetR_mutants/MITOMI_data"