Difference between revisions of "Team:Tsinghua-A/Improve"

 
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                         Improved part
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                         Improve
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                     <h2>Improvement of a previous part </h2>
 
                     <h2>Improvement of a previous part </h2>
 
                     <p>BBa_K511401 HRH4-TEVs-GV16 Signaling Receptor MammoBlock (created by Group: iGEM11_MIT 2011-09-27)</p>
 
                     <p>BBa_K511401 HRH4-TEVs-GV16 Signaling Receptor MammoBlock (created by Group: iGEM11_MIT 2011-09-27)</p>
 
                     <p>We based on this part, kept the coding sequence of HRH4 and added a new promoter ADH1, a new tag mcherry and ADH1 terminator. Then, we got our new part BBa_K2583001, in our project, its function is not related the original one, it is used to test the expression and the location of human histamine receptor H4 (HRH4) in yeast, it lays the foundation for the subsequent experiments. </p>
 
                     <p>We based on this part, kept the coding sequence of HRH4 and added a new promoter ADH1, a new tag mcherry and ADH1 terminator. Then, we got our new part BBa_K2583001, in our project, its function is not related the original one, it is used to test the expression and the location of human histamine receptor H4 (HRH4) in yeast, it lays the foundation for the subsequent experiments. </p>
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                    <h3> More Information </h3>
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                    <p><a href="http://parts.igem.org/Part:BBa_K511401"><u>BBa_K511401</u></a></p>
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                    <p><a href="http://parts.igem.org/Part:BBa_K2583001"><u>BBa_K2583001</u></a></p>
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                     <h2>Experiment</h2>
 
                     <h2>Experiment</h2>
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                     <ol>
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                     <h3>Fluorescence microscopy</h3>
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                    <li>Fluorescence microscopy</li>
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                     <p>After transforming the CENPK2-1C ura3::far1 his2::sst2 trp3::ste2 △ura3 Saccharomyces cerevisiae with plasmid pGADT7 contains part BBa_K2583001, 30℃ cultivate on △leu solid medium for one day. Select monoclonal and enlarge culture overnight, then observe the fluorescence under the microscope with 580nm exciting light. The red fluorescence shows the expression of HRH4-mcherry fusion protein.</p>
 
                     <p>After transforming the CENPK2-1C ura3::far1 his2::sst2 trp3::ste2 △ura3 Saccharomyces cerevisiae with plasmid pGADT7 contains part BBa_K2583001, 30℃ cultivate on △leu solid medium for one day. Select monoclonal and enlarge culture overnight, then observe the fluorescence under the microscope with 580nm exciting light. The red fluorescence shows the expression of HRH4-mcherry fusion protein.</p>
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                    <p>Figure1. the fluorescence microscopy result of HRH4-mcherry</p>
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                            <img src="https://static.igem.org/mediawiki/2018/a/ab/T--Tsinghua-A--improve-improveFig1.png" alt="" height="700" width="700"/>
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                            <p>Figure1. the fluorescence microscopy result of HRH4-mcherry</p>
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                     <p>In order to find out if HRH4 can be expressed correctly in yeast’s membrane, DIO, a kind of Green fluorescent probe of cell membrane, is add to the yeast. In figure 2, it shows that the most of the red HRH4-mcherry colocalized with DIO in the membrane, it indicates there are quite a few HRH4-mcherry fusion proteins have correct localization. </p>
 
                     <p>In order to find out if HRH4 can be expressed correctly in yeast’s membrane, DIO, a kind of Green fluorescent probe of cell membrane, is add to the yeast. In figure 2, it shows that the most of the red HRH4-mcherry colocalized with DIO in the membrane, it indicates there are quite a few HRH4-mcherry fusion proteins have correct localization. </p>
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                    <p>Figure 2. the fluorescence microscopy result of DIO dying and HRH4-mcherry</p>
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                            <img src="https://static.igem.org/mediawiki/2018/8/86/T--Tsinghua-A--improve-improveFig2.png" alt="" height="700" width="700"/>
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                            <p>Figure 2. the fluorescence microscopy result of DIO dying and HRH4-mcherry</p>
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                     <li>Flow CytoMetry (FCM)</li>
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                     <h3>Flow CytoMetry (FCM)</h3>
 
                     <p>From the result of fluorescence microscopy, the expression of HRH4-mcherry fusion proteins can be observed roughly, for measuring the expression level of HRH4-mcherry, FCM is performed. From the result, a distinct peak value can be observed. Though it can’t representative all the functional HRH4 that locates in the membrane, it can be indicated that most of them are correctly located from the fluorescence microscopy result, this data is enough to support our modeling.</p>
 
                     <p>From the result of fluorescence microscopy, the expression of HRH4-mcherry fusion proteins can be observed roughly, for measuring the expression level of HRH4-mcherry, FCM is performed. From the result, a distinct peak value can be observed. Though it can’t representative all the functional HRH4 that locates in the membrane, it can be indicated that most of them are correctly located from the fluorescence microscopy result, this data is enough to support our modeling.</p>
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                     <h2>Result</h2>
 
                     <h2>Result</h2>
 
                     <p>The test of this composite part set the foundation of our project, it proved that HRH4 can be expressed in high level under the trigger of a constitutive promoter-ADH1 promoter. Besides, the HRH4 can locate in the yeasts’ membrane without adding other sequence. It can be indicated that if mcherry is removed, functional HRH4 can still be expressed and locate in the membrane.</p>
 
                     <p>The test of this composite part set the foundation of our project, it proved that HRH4 can be expressed in high level under the trigger of a constitutive promoter-ADH1 promoter. Besides, the HRH4 can locate in the yeasts’ membrane without adding other sequence. It can be indicated that if mcherry is removed, functional HRH4 can still be expressed and locate in the membrane.</p>
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Latest revision as of 16:48, 17 October 2018

Improve

Improvement of a previous part

BBa_K511401 HRH4-TEVs-GV16 Signaling Receptor MammoBlock (created by Group: iGEM11_MIT 2011-09-27)

We based on this part, kept the coding sequence of HRH4 and added a new promoter ADH1, a new tag mcherry and ADH1 terminator. Then, we got our new part BBa_K2583001, in our project, its function is not related the original one, it is used to test the expression and the location of human histamine receptor H4 (HRH4) in yeast, it lays the foundation for the subsequent experiments.

More Information

BBa_K511401

BBa_K2583001

Experiment

Fluorescence microscopy

After transforming the CENPK2-1C ura3::far1 his2::sst2 trp3::ste2 △ura3 Saccharomyces cerevisiae with plasmid pGADT7 contains part BBa_K2583001, 30℃ cultivate on △leu solid medium for one day. Select monoclonal and enlarge culture overnight, then observe the fluorescence under the microscope with 580nm exciting light. The red fluorescence shows the expression of HRH4-mcherry fusion protein.

Figure1. the fluorescence microscopy result of HRH4-mcherry

In order to find out if HRH4 can be expressed correctly in yeast’s membrane, DIO, a kind of Green fluorescent probe of cell membrane, is add to the yeast. In figure 2, it shows that the most of the red HRH4-mcherry colocalized with DIO in the membrane, it indicates there are quite a few HRH4-mcherry fusion proteins have correct localization.

Figure 2. the fluorescence microscopy result of DIO dying and HRH4-mcherry

Flow CytoMetry (FCM)

From the result of fluorescence microscopy, the expression of HRH4-mcherry fusion proteins can be observed roughly, for measuring the expression level of HRH4-mcherry, FCM is performed. From the result, a distinct peak value can be observed. Though it can’t representative all the functional HRH4 that locates in the membrane, it can be indicated that most of them are correctly located from the fluorescence microscopy result, this data is enough to support our modeling.

Result

The test of this composite part set the foundation of our project, it proved that HRH4 can be expressed in high level under the trigger of a constitutive promoter-ADH1 promoter. Besides, the HRH4 can locate in the yeasts’ membrane without adding other sequence. It can be indicated that if mcherry is removed, functional HRH4 can still be expressed and locate in the membrane.

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