Abstract
Phage display strategy has been used for selection of scFv antibodies
that recognize cell surface tumour-associated antigens expressed in human
breast cancer cells. The human naïve scFv library was first depleted with
normal cell lines to remove those antibodies that bind to common cell surface
epitopes. The antibody selection was not target-driven; instead selected
antibodies will be used to identify new cancer related cell surface antigens
which could have applications both in cancer therapy and diagnostic. 15
different scFv antibodies with preferential binding specificity towards MCF-7
breast cancer cell line have been isolated. The potential antigens will be
immunoprecipitated from MCF-7 lysates with biotinylated scFvs immobilized to
streptavidin coated magnetic beads and identified by mass spectrometry. We
have also isolated metastasis related antibodies by using whole cell panning
procedure to a pair of monoclonal cell lines that have opposite metastatic
capabilities in immunocompromised mice. GD8 cell line is tumorigenic and more
aggressively metastatic to the lungs than parent cell line while BD12 cell
line is totally nonmetastatic but equally tumorigenic in athymic mice. Five
different scFv clones binding more strongly to GD8 cell line that BD12 cell
line has been isolated, and their functions and target antigens are under
investigation.
Original language | English |
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Publication status | Published - 2005 |
MoE publication type | Not Eligible |
Event | Next-Generation Protein Therapeutics - Basel, Switzerland Duration: 8 Nov 2005 → 9 Nov 2005 |
Conference
Conference | Next-Generation Protein Therapeutics |
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Country/Territory | Switzerland |
City | Basel |
Period | 8/11/05 → 9/11/05 |