Abstract | BACKGROUND: METHODS: A renal carcinoma cell line A498 and a normal renal cell line HK-2 were used to carry out subtractive screening in vitro with a phage display peptide library. After three rounds of panning, there was an obvious enrichment for the phages specifically binding to the A498 cells, and the output/input ratio of phages increased about 100 fold. A group of peptides capable of binding specifically to the renal carcinoma cells were obtained, and the affinity of these peptides to the targeting cells and tissues was studied. RESULTS: Through a cell-based ELISA, immunocytochemical staining, immunohistochemical staining, and immunofluorescence, the Phage ZT-2 and synthetic peptide ZT-2 were shown to specifically bind to the tumor cell surfaces of A498 and incision specimens, but not to normal renal tissue samples. CONCLUSION:
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Authors | Xiangan Tu, Jintao Zhuang, Wenwei Wang, Liang Zhao, Liangyun Zhao, Jiquan Zhao, Chunhua Deng, Shaopeng Qiu, Yuanyuan Zhang |
Journal | Journal of experimental & clinical cancer research : CR
(J Exp Clin Cancer Res)
Vol. 30
Pg. 105
(Nov 10 2011)
ISSN: 1756-9966 [Electronic] England |
PMID | 22071019
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Retracted Publication)
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Chemical References |
- Oligopeptides
- Peptide Library
- Peptides
- peptide ZT-2
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Topics |
- Amino Acid Sequence
- Binding, Competitive
- Carcinoma, Renal Cell
(metabolism)
- Cell Line
- Enzyme-Linked Immunosorbent Assay
- Humans
- Kidney Neoplasms
(metabolism)
- Oligopeptides
(metabolism)
- Peptide Library
- Peptides
(chemistry, metabolism)
- Protein Binding
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