Difference between revisions of "Part:BBa K3771009"
Line 6: | Line 6: | ||
<br> | <br> | ||
− | <br>The OmpA/OprF chimeric protein consists of amino acid sequences from both OmpA transmembrane protein from E. coli and OprF porin protein from P. aeruginosa [1, | + | <br>The OmpA/OprF chimeric protein consists of amino acid sequences from both OmpA transmembrane protein from <i>E. coli</i> and OprF porin protein from <i>P. aeruginosa</i> [1,2]. The newly added loop from OprF allows OmpA/OprF chimeric protein to bind to IFN-γ and initiate a signal transduction to the inner membrane [4].<br> |
− | to | + | <br><b style="font-size:1.3rem">Biology</b> |
+ | <br> | ||
+ | |||
+ | <div style="width=100%; display:flex; align-items: center; justify-content: center;"> | ||
+ | <img src="https://2021.igem.org/File:T--NCKU_Tainan--ompA_oprF.gif" style="width:35%;"> | ||
+ | </div> | ||
+ | <p align="center">Figure 1: Construction of OmpA/OprF chimeric protein</p> | ||
+ | |||
+ | |||
+ | <br>One of the innate functions of OprF is the capability to bind and respond to IFN-γ. Of the four β-barrel loops in OmpA, the first loop is removed and replaced by a loop from OprF, resulting in an OmpA protein with a section of OprF protein. The new extracellular peptides of the OmpA/OprF chimeric protein allows for binding of IFN-γ to the <i>E. coli</i> outer membrane, initiating the phage shock protein (Psp) system and its signal transduction to the inner membrane [3].<br> | ||
+ | |||
+ | <br><b style="font-size:1.3rem">Usage</b> | ||
+ | <br> | ||
+ | |||
+ | <br>In the IFN-γ sensing system, OmpA/OprF chimeric protein expression is regulated by the <i>ompA</i> promoter. Binding of IFN-γ to the OmpA/OprF chimeric protein activates the <i>pspA</i> promoter, producing the enzyme required for the synthesis of taurine. <br> | ||
+ | |||
+ | <br><b style="font-size:1.3rem">Characterization</b> | ||
+ | <br> | ||
+ | |||
+ | <br>The <i>ompA/oprF</i> sequence was synthesized by IDT and amplified by PCR. Agarose gel electrophoresis result is shown in Fig. 2.<br> | ||
+ | |||
+ | <div style="width=100%; display:flex; align-items: center; justify-content: center;"> | ||
+ | <img src="https://2021.igem.org/wiki/images/f/fd/T--NCKU_Tainan--pcr_ompA_oprF.gif.jpg" style="width:35%;"> | ||
+ | </div> | ||
+ | <p align="center">圖片描述</p> | ||
+ | |||
+ | <br>Expression of OmpA/OprF chimeric protein was confirmed by western blot using anti-OmpA antibody.<br> | ||
+ | |||
+ | <div style="width=100%; display:flex; align-items: center; justify-content: center;"> | ||
+ | <img src="https://2021.igem.org/wiki/images/9/9b/T--NCKU_Tainan--results_ompA_wb.jpg" style="width:35%;"> | ||
+ | </div> | ||
+ | <p align="center">圖片描述</p> | ||
+ | |||
+ | |||
+ | <br><b style="font-size:1.3rem">References</b> | ||
+ | <br>1. Wang Y. The Function of OmpA in Escherichia coli. Biochemical and Biophysical Research Communications. 2002;292(2):396-401. doi:10.1006/bbrc.2002.6657 | ||
+ | https://pubmed.ncbi.nlm.nih.gov/11906175/ | ||
+ | |||
+ | <br>2. Wu L. Recognition of Host Immune Activation by Pseudomonas aeruginosa. Science. 2005;309(5735):774-777. doi:10.1126/science.1112422 | ||
+ | https://pubmed.ncbi.nlm.nih.gov/16051797/ | ||
+ | |||
+ | <br>3. Aurand TC, March JC. Development of a synthetic receptor protein for sensing inflammatory mediators interferon‐γ and tumor necrosis factor‐α. Biotechnology and Bioengineering. 2016;113(3):492-500. doi:10.1002/bit.25832 | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 12:15, 18 October 2021
OmpA/OprF chimeric protein
Description
The OmpA/OprF chimeric protein consists of amino acid sequences from both OmpA transmembrane protein from E. coli and OprF porin protein from P. aeruginosa [1,2]. The newly added loop from OprF allows OmpA/OprF chimeric protein to bind to IFN-γ and initiate a signal transduction to the inner membrane [4].
Biology
<img src="https://2021.igem.org/File:T--NCKU_Tainan--ompA_oprF.gif" style="width:35%;">
Figure 1: Construction of OmpA/OprF chimeric protein
One of the innate functions of OprF is the capability to bind and respond to IFN-γ. Of the four β-barrel loops in OmpA, the first loop is removed and replaced by a loop from OprF, resulting in an OmpA protein with a section of OprF protein. The new extracellular peptides of the OmpA/OprF chimeric protein allows for binding of IFN-γ to the E. coli outer membrane, initiating the phage shock protein (Psp) system and its signal transduction to the inner membrane [3].
Usage
In the IFN-γ sensing system, OmpA/OprF chimeric protein expression is regulated by the ompA promoter. Binding of IFN-γ to the OmpA/OprF chimeric protein activates the pspA promoter, producing the enzyme required for the synthesis of taurine.
Characterization
The ompA/oprF sequence was synthesized by IDT and amplified by PCR. Agarose gel electrophoresis result is shown in Fig. 2.
<img src="" style="width:35%;">
圖片描述
Expression of OmpA/OprF chimeric protein was confirmed by western blot using anti-OmpA antibody.
<img src="" style="width:35%;">
圖片描述
References
1. Wang Y. The Function of OmpA in Escherichia coli. Biochemical and Biophysical Research Communications. 2002;292(2):396-401. doi:10.1006/bbrc.2002.6657
https://pubmed.ncbi.nlm.nih.gov/11906175/
2. Wu L. Recognition of Host Immune Activation by Pseudomonas aeruginosa. Science. 2005;309(5735):774-777. doi:10.1126/science.1112422
https://pubmed.ncbi.nlm.nih.gov/16051797/
3. Aurand TC, March JC. Development of a synthetic receptor protein for sensing inflammatory mediators interferon‐γ and tumor necrosis factor‐α. Biotechnology and Bioengineering. 2016;113(3):492-500. doi:10.1002/bit.25832
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 813
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]