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Team:USTC CHINA/Project/AdvancingWork
From 2013.igem.org
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<img src="https://static.igem.org/mediawiki/2013/2/22/DSC_0106.jpg"></br></br> | <img src="https://static.igem.org/mediawiki/2013/2/22/DSC_0106.jpg"></br></br> | ||
<div class="atfigure" align="center" style="width:580px; font-size:14px">Fig7. This is where we conducted mice experiments,Specefic pathogen Free(SPF) Experiment Center</div> | <div class="atfigure" align="center" style="width:580px; font-size:14px">Fig7. This is where we conducted mice experiments,Specefic pathogen Free(SPF) Experiment Center</div> | ||
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<div class="atfigure" align="center" style="width:580px; font-size:14px">Fig8. Our lab-gown</div> | <div class="atfigure" align="center" style="width:580px; font-size:14px">Fig8. Our lab-gown</div> | ||
| - | <img src="https://static.igem.org/mediawiki/2013/0/02/DSC_0088.jpg"></br></br> | + | <img src="https://static.igem.org/mediawiki/2013/0/02/DSC_0088.jpg" align="center"></br></br> |
<div class="atfigure" align="center" style="width:580px; font-size:14px">Fig9. We were observing mice</div> | <div class="atfigure" align="center" style="width:580px; font-size:14px">Fig9. We were observing mice</div> | ||
<img src="https://static.igem.org/mediawiki/2013/0/02/DSC_0109.jpg"></br></br> | <img src="https://static.igem.org/mediawiki/2013/0/02/DSC_0109.jpg"></br></br> | ||
Revision as of 05:21, 28 October 2013
Introduction
According to our experiment result, we have proved the secretion and expression possibility of TD1-antigen, TD1-adjuvant, and the antigenicity of TD1-antigen after transdermal process. So in the following experiments, we decided to utilize B.subtilis WB800N as engineered bacteria, plus shuttle vector pHT43 as secretion vector to build the B.subtilis secretory expression system. On top of this, we have taken advantage of different kinds of TD1-antigen, testing HBsAg, PA, Ag85b that have been applied into the market to check the universal property of TD1-antigen. Besides, reporters essential during real application have been found to realize the final circuit.
ONE: Expression of TD1-"X" in WB800N
1.Expression of TD1-GFP
2.Expression of TD1-antigen/adjuvant
In order to realize the secretory expression in B.subtilis, we inserted signal peptide between promoter and the TD1-Antigen/adjuvant sequence to secrete our recombinant protein. GFP was chosen to check the reliability of this circuit. After large amounts of experiments, GFP has finally been found via fluorescence microscope.
Then, three kinds of recombinant antigen, TD1-HBsAg, TD1-PA, TD1-Ag85b, and recombinant immunologic adjuvant were designed. The earliest successful protein TD1-LTB can not only be observed clear stripes in SDS-PAGE, but also be proved according to HPLC-MS.
TWO: Neomycin resistance of WB800N
Selection on the of resistance of B.subtilis WB800N against neomycin
As WB800N is a novel secretory expression system, most of whose parameters remain unclear, among which the chief problem is that its unique resistance against neomycin has never been quantitatively analyzed, and our work made up for this blank.
We have figured it out that the best concentration of neomycin for selection use is 128mg/ml.
THREE: Mice Experiment is in Progress
Specific Pathogen Free (SPF) Laboratory
Specific Pathogen Free is a term used for laboratory animals that are guaranteed free of particular pathogens. Use of SPF animals ensures that specified diseases do not interfere with an experiment. For example, absence of respiratory pathogens such as influenza is desirable when investigating a drug's effect on lung function.
