Abstract
Therapeutic approaches aimed at targeting tumor surface markers using monoclonal antibodies provide a powerful strategy in cancer treatment. Here we report selection of single variable domains (VHH) of llama heavy chain antibodies, using a VHH-phage-display library. A reverse proteomic approach was used to identify the cognate proteins recognized by enriched VHH on HeLa cells. One of these VHH bound the integrin α3β1 (VLA-3) and was further characterized. Most interestingly, this VHH could inhibit VLA-3 mediated cell-matrix adhesion. Our approach provides a fast and efficient method to screen for novel cell surface markers on normal and tumor cells that may find diagnostic or therapeutic application in disease management or treatment.
Original language | English (US) |
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Pages (from-to) | 2022-2028 |
Number of pages | 7 |
Journal | Molecular Immunology |
Volume | 46 |
Issue number | 10 |
DOIs | |
State | Published - Jun 2009 |
Externally published | Yes |
Keywords
- Anti adhesive VHH
- Integrin
- Phage-display
- Surface marker
- VLA-3
ASJC Scopus subject areas
- Immunology
- Molecular Biology