TY - JOUR
T1 - Construction of human monoclonal single-chain Fv antibodies against small-cell lung cancer by phage display libraries derived from cell-immunized SCID mice engrafted with human peripheral blood lymphocytes
AU - Douguchi, Junya
AU - Hashiguchi, Akinori
AU - Sakamoto, Michiie
PY - 2009/12
Y1 - 2009/12
N2 - In this study, we describe a phage display strategy to obtain human monoclonal single-chain Fv (scFv) antibodies binding target cancer cell surface proteins. By developing a cancer cell immunization protocol for SCID mice engrafted with human peripheral blood lymphocytes in combination with an antibody phage display method, we have isolated phage antibodies binding small-cell lung cancer cell line H889 by subtractive selection. One of the isolated scFv antibodies, 12EAb, recognized the E2 component of pyruvate dehydrogenase complex (PDC-E2) by immunoprecipitation according to MALDI-TOF MS analysis. Furthermore, we have confirmed the plasma membrane localization of PDC-E2 in small-cell lung cancer cells by immunocytochemistry and cell surface protein biotinylation, although PDC-E2 is usually located in the mitochondrial matrix. These results, including unique localization of identified antigens, were obtained by proteomic approaches. The present methods can be applied to generate human monoclonal scFv antibodies against tumor cells and to identify new mole- cular targets for immunotherapy and markers for diagnosis.
AB - In this study, we describe a phage display strategy to obtain human monoclonal single-chain Fv (scFv) antibodies binding target cancer cell surface proteins. By developing a cancer cell immunization protocol for SCID mice engrafted with human peripheral blood lymphocytes in combination with an antibody phage display method, we have isolated phage antibodies binding small-cell lung cancer cell line H889 by subtractive selection. One of the isolated scFv antibodies, 12EAb, recognized the E2 component of pyruvate dehydrogenase complex (PDC-E2) by immunoprecipitation according to MALDI-TOF MS analysis. Furthermore, we have confirmed the plasma membrane localization of PDC-E2 in small-cell lung cancer cells by immunocytochemistry and cell surface protein biotinylation, although PDC-E2 is usually located in the mitochondrial matrix. These results, including unique localization of identified antigens, were obtained by proteomic approaches. The present methods can be applied to generate human monoclonal scFv antibodies against tumor cells and to identify new mole- cular targets for immunotherapy and markers for diagnosis.
KW - PDC-E2
KW - Phage display
KW - SCID mice engrafted with human peripheral blood lymphocytes
KW - Single-chain Fv
KW - Small-cell lung cancer
UR - http://www.scopus.com/inward/record.url?scp=77951085616&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77951085616&partnerID=8YFLogxK
U2 - 10.1002/prca.200900060
DO - 10.1002/prca.200900060
M3 - Article
C2 - 21136949
AN - SCOPUS:77951085616
SN - 1862-8346
VL - 3
SP - 1265
EP - 1272
JO - Proteomics - Clinical Applications
JF - Proteomics - Clinical Applications
IS - 11
ER -