Specificity grafting of human antibody frameworks selected from a phage display library: generation of a highly stable humanized anti-CD22 single-chain Fv fragment

@article{citeulike:812979, abstract = {A prerequisite for the enrichment of antibodies screened from phage display libraries is their stable expression on a phage during multiple selection rounds. Thus, if stringent panning procedures are employed, selection is simultaneously driven by antigen affinity, stability and solubility. To take advantage of robust pre-selected scaffolds of such molecules, we grafted single-chain Fv (scFv) antibodies, previously isolated from a human phage display library after multiple rounds of in vitro panning on tumor cells, with the specificity of the clinically established murine monoclonal anti-CD22 antibody RFB4. We show that a panel of grafted scFvs retained the specificity of the murine monoclonal antibody, bound to the target antigen with high affinity (6.4-9.6 nM), and exhibited exceptional biophysical stability with retention of 89-93\% of the initial binding activity after 6 days of incubation in human serum at 37{degrees}C. Selection of stable human scaffolds with high sequence identity to both the human germline and the rodent frameworks required only a small number of murine residues to be retained within the human frameworks in order to maintain the structural integrity of the antigen binding site. We expect this approach may be applicable for the rapid generation of highly stable humanized antibodies with low immunogenic potential. 10.1093/protein/gzg096}, author = {Krauss, Jurgen and Arndt, Michaela A. and Martin, Andrew C. and Liu, Huaitian and Rybak, Susanna M. }, citeulike-article-id = {812979}, journal = {Protein Eng.}, keywords = {protein-engineering, protein-stability}, month = {October}, number = {10}, pages = {753--759}, posted-at = {2006-08-22 20:37:14}, priority = {2}, title = {Specificity grafting of human antibody frameworks selected from a phage display library: generation of a highly stable humanized anti-CD22 single-chain Fv fragment}, url = {http://peds.oxfordjournals.org/cgi/content/abstract/16/10/753}, volume = {16}, year = {2003} }

TY - JOUR ID - citeulike:812979 L3 - citeulike-article-id:812979 TI - Specificity grafting of human antibody frameworks selected from a phage display library: generation of a highly stable humanized anti-CD22 single-chain Fv fragment JF - Protein Eng. VL - 16 IS - 10 SP - 753 EP - 759 N2 - A prerequisite for the enrichment of antibodies screened from phage display libraries is their stable expression on a phage during multiple selection rounds. Thus, if stringent panning procedures are employed, selection is simultaneously driven by antigen affinity, stability and solubility. To take advantage of robust pre-selected scaffolds of such molecules, we grafted single-chain Fv (scFv) antibodies, previously isolated from a human phage display library after multiple rounds of in vitro panning on tumor cells, with the specificity of the clinically established murine monoclonal anti-CD22 antibody RFB4. We show that a panel of grafted scFvs retained the specificity of the murine monoclonal antibody, bound to the target antigen with high affinity (6.4-9.6 nM), and exhibited exceptional biophysical stability with retention of 89-93% of the initial binding activity after 6 days of incubation in human serum at 37{degrees}C. Selection of stable human scaffolds with high sequence identity to both the human germline and the rodent frameworks required only a small number of murine residues to be retained within the human frameworks in order to maintain the structural integrity of the antigen binding site. We expect this approach may be applicable for the rapid generation of highly stable humanized antibodies with low immunogenic potential. 10.1093/protein/gzg096 KW - protein-engineering KW - protein-stability AU - Krauss, Jurgen AU - Arndt, Michaela AU - Martin, Andrew AU - Liu, Huaitian AU - Rybak, Susanna PY - 2003/10/01/ UR - http://peds.oxfordjournals.org/cgi/content/abstract/16/10/753 ER -