Skip to content
Snippets Groups Projects
Commit edd5a04f authored by Zonghan Liu's avatar Zonghan Liu
Browse files

Update wiki/pages/collaborations.html

parent 6153a1d5
No related branches found
No related tags found
No related merge requests found
Pipeline #99166 passed
......@@ -207,7 +207,7 @@
<div>1. The structure of anchor protein and passenger protein is easy to affect each other, interferes with their correct folding, and reduces the activity of passenger protein </div>
<div>2. Different transporter proteins will affect the physiological function of the recipient bacteria (growth instability, etc.)</div>
<div>After filtering these required properties, we obtained several satisfied anchor proteins: </div>
<div>其他可用的蛋白</div>
<div>Lipoprotein, S-layer protein and INP.</div>
<div>From them, also followed the instructions given by our advisors, we eventually decided to use ice-nucleation protein, since its advantages in cell surface display technology:</div>
</div>
<div class="title2" style="font-weight: bold;">-Pros of INP</div>
......@@ -271,6 +271,12 @@
</div>
<div class="title2">
&emsp;&emsp;We accomplished this section together, not only for better effectiveness but also to allow our three teams to bring out our diverse strengths, to make a greater performance. Moreover, more audiences are involved because we separately propagandize the lectures. These advantages can be only shown between team collaboration, therefore we are able to achieve a better job.
References
</div>
<div class='title2'>
<div>1. 1. 李茜茜. 利用冰晶核蛋白构建细菌细胞表面展示体系及其应用研究[D]. 湖北:华中农业大学,2009. DOI:10.7666/d.y1805378.</div>
<div>2. 2. Zhang, Z. et al. (2016) Surface immobilization of human arginase-1 with an engineered ice nucleation protein display system in E. coli, PloS one. Public Library of Science. </div>
</div>
</div>
</div>
......
0% Loading or .
You are about to add 0 people to the discussion. Proceed with caution.
Finish editing this message first!
Please register or to comment