Team:Potsdam Bioware
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+ | !align="center"|[[Team:Potsdam_Bioware|Home]] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Team|Team]] | ||
+ | !align="center"|[https://igem.org/Team.cgi?year=2012&team_name=Potsdam_Bioware Official Team Profile] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Project|Project]] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Parts|Parts Submitted to the Registry]] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Modeling|Modeling]] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Notebook|Notebook]] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Safety|Safety]] | ||
+ | !align="center"|[[Team:Potsdam_Bioware/Attributions|Attributions]] | ||
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==Direct Antibody Identification, Maturation and Production in CHO-Cells== | ==Direct Antibody Identification, Maturation and Production in CHO-Cells== | ||
Revision as of 21:09, 24 August 2012
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Direct Antibody Identification, Maturation and Production in CHO-Cells
Project Description
Antibodies are versatile molecules for research and therapy and they are currently revolutionizing the market of biopharmaceuticals. To date, antibodies are generated in a laborious and time consuming manner. Either animal immunization followed by hybridoma technology or phage display is used to identify desired genes, which then need to be transferred to a production cell line such as CHO. We designed a streamlined workflow that incorporates all steps of antibody generation in CHO cells. Our plan is to stably transfect an antibody-fragment library in CHO cells. Antibody maturation is mimicked by further diversifying this library using the enzyme Activation-Induced cytidine Deaminase (AID), which is known to induce somatic hypermutation. Next, we plan to test and deploy a versatile and continuous viral selection system for clones producing the desired antibodies. Finally, we will try to employ a genetic switch to go from surface expression to soluble production of antibodies.
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