Team:Potsdam Bioware

From 2012.igem.org

(Difference between revisions)
(Project Description)
(Project Description)
Line 1: Line 1:
==Direct Antibody Identification, Maturation and Production in CHO-Cells==
==Direct Antibody Identification, Maturation and Production in CHO-Cells==
-
===Project Description===
 
 +
<div class="box_round">
 +
===Project Description===
 +
<hr/>
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.
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.
-
 
+
</div>
<html><center>
<html><center>
Line 62: Line 64:
!align="center"|[[Team:Potsdam_Bioware/Attributions|Attributions]]
!align="center"|[[Team:Potsdam_Bioware/Attributions|Attributions]]
|}
|}
 +
 +
<html>
 +
<head>
 +
<style type="text/css">
 +
 +
.box_round {
 +
  color: white;
 +
  padding: 5px;
 +
  border-radius: 15px;
 +
  background: #cb9840;
 +
  background: -moz-linear-gradient(top,  #cb9840 0%, #a77b34 100%);
 +
  background: -webkit-gradient(linear, left top, left bottom, color-stop(0%,#cb9840), color-stop(100%,#a77b34));
 +
  background: -webkit-linear-gradient(top,  #cb9840 0%,#a77b34 100%);
 +
  background: -o-linear-gradient(top,  #cb9840 0%,#a77b34 100%);
 +
  background: -ms-linear-gradient(top,  #cb9840 0%,#a77b34 100%);
 +
  background: linear-gradient(to bottom,  #cb9840 0%,#a77b34 100%);
 +
  filter: progid:DXImageTransform.Microsoft.gradient( startColorstr='#cb9840', endColorstr='#a77b34',GradientType=0 );
 +
  box-shadow:8px 8px 8px #666;
 +
}
 +
</head>
 +
</html>

Revision as of 20:33, 24 August 2012

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.


Home Team Official Team Profile Project Parts Submitted to the Registry Modeling Notebook Safety Attributions