Difference between revisions of "Team:Jiangnan"
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<p>The goal of our project is to enable 3 features of our chassis cell, i.e.</p> | <p>The goal of our project is to enable 3 features of our chassis cell, i.e.</p> | ||
<p>high titration, suspension cultivation, and broad spectrum to reduce the production cost and increase the yield of viruses for vaccine production.</p> | <p>high titration, suspension cultivation, and broad spectrum to reduce the production cost and increase the yield of viruses for vaccine production.</p> | ||
| − | <p>The chassis cell we used here is | + | <p>The chassis cell we used here is MDBK cells.</p> |
</div> | </div> | ||
</div> | </div> | ||
Revision as of 10:00, 28 June 2018
Project Description
The limiting factors of most vaccine companies, according to our previous invesigation and survey.are multifaceted costs in actual production process and long product life cycle and other issues due to complex application process of new vaccines(cell line).
The goal of our project is to enable 3 features of our chassis cell, i.e.
high titration, suspension cultivation, and broad spectrum to reduce the production cost and increase the yield of viruses for vaccine production.
The chassis cell we used here is MDBK cells.
Through bioinformatics analysis and mathematical modeling, we constructed the network regulating virus titration of cells. The top gene was selected, functionally validated in vitro and used for genomic modulation in the chassis cells to enable them the feature of increased titration. On the other hand, we manufactured a device to generate cold atmospheric plasma, using which cell titration was further increased in response to plasma irradiation.
Through high throughput sequencing of two pairs of cells with and without the suspension feature, we found a panel of genes responsible for the suspension feature of cells following network construction using computational approach. The top gene was functionally validated before applied to the chassis cell for genomic modulation.
Through text mining, we classified cell receptors according to the Baltimore subtyping of viruses and summarized the primary receptors mediating the entry of different types of viruses. After systematic analysis, we aim to express Nectin 4 and Tfr on our chassis cells to make them possible to a broad spectrum of viruses.
