Difference between revisions of "Team:NUDT CHINA/Model"
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<h1 style="font-size: 40px;font-weight: 900">Our Work</h1> | <h1 style="font-size: 40px;font-weight: 900">Our Work</h1> | ||
| − | + | <p alt="content_add" style="font-size: 18px;"> Our innovative project present a target protein disruption method in order to degrade endogenous target proteins acutely in mammalian cells.To explain and predict the possibilities within the wetlab limits，we built ODE models and applied our measured data to parameters simulation method based on Bayesian parameter estimation to obtain parameters which fits our reality better. We use this model to obtain the relation between the expression time of plasmid and protein degradation rate,making it accessible to future teams who want to incorporate our minds into their designs.Through the modeling ,we understand the reaction mechanism more specifically and obtain how different factors influence the degradation process .This model also offers guidelines on choosing detection point and future clinical application. </p> | |
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| − | <img alt="300x200" src="https://static.igem.org/mediawiki/2018/9/9b/2018_igem_menu_logo.svg" /> | + | <a href="https://2018.igem.org/Team:NUDT_CHINA/Model/Overview#model1"> <img alt="300x200" src="https://static.igem.org/mediawiki/2018/9/9b/2018_igem_menu_logo.svg" /> </a> |
| − | <p alt="photo_detail" style="text-align: center;">This is the | + | <p alt="photo_detail" style="text-align: center;">This is the model1!</p> |
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| − | < | + | <!-- <p class="text-center text-info">this is the sign of igem</p> --> |
| − | + | <p alt="photo_detail" style="text-align: center;"><em>model2</em></p> | |
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| − | + | <p alt="photo_detail" style="text-align: center;"><em>model3</em></p> | |
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| − | <img alt="300x200" src="https://static.igem.org/mediawiki/2018/9/9b/2018_igem_menu_logo.svg" /> | + | <a href="https://2018.igem.org/Team:NUDT_CHINA/Model/Overview#model2"> <img alt="300x200" src="https://static.igem.org/mediawiki/2018/9/9b/2018_igem_menu_logo.svg"> </a> |
| + | </div> | ||
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| + | <a href="https://2018.igem.org/Team:NUDT_CHINA/Model/Overview#model3"> <img alt="300x200" src="https://static.igem.org/mediawiki/2018/9/9b/2018_igem_menu_logo.svg"> </a> | ||
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<h3>More details</h3> | <h3>More details</h3> | ||
Revision as of 00:52, 4 October 2018
Development of A Novel
Blood-MicroRNA Handy Detection System with CRISPR
Our Work
Our innovative project present a target protein disruption method in order to degrade endogenous target proteins acutely in mammalian cells.To explain and predict the possibilities within the wetlab limits，we built ODE models and applied our measured data to parameters simulation method based on Bayesian parameter estimation to obtain parameters which fits our reality better. We use this model to obtain the relation between the expression time of plasmid and protein degradation rate,making it accessible to future teams who want to incorporate our minds into their designs.Through the modeling ,we understand the reaction mechanism more specifically and obtain how different factors influence the degradation process .This model also offers guidelines on choosing detection point and future clinical application.
This is the model1!
model2
model3
More details
There are several variants of derived from different organisms. In our project, we . The structure of this protein has been determined with and without The a lobe. The two lobes are positively charged towards the protein core to accommodate the negatively charged RNA. Each of these two lobes contains an RNase domain. At the main is responsible for target cleavage. In contrast to other two RNase domains of the NUC lobe are located at the outside of the protein, which is likely the reason collateral cleavage upon activation by binding to a matching target. These two domains have been labeled as red spots in Figure 2 and can be found at the interface between the green and pink domain.
Anim pariatur cliche...