Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 1265-1272 |
| Number of pages | 8 |
| Journal | Proteomics - Clinical Applications |
| Volume | 3 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 2009 Dec |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- PDC-E2
- Phage display
- SCID mice engrafted with human peripheral blood lymphocytes
- Single-chain Fv
- Small-cell lung cancer
ASJC Scopus subject areas
- Clinical Biochemistry
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