Identification and characterization of a novel phage display-derived peptide with affinity for human brain metastatic breast cancer

被引:0
作者
Bo Fu
Ying Zhang
Wei Long
Aifeng Zhang
Yafen Zhang
Yanli An
Fengqin Miao
Fang Nie
Mingli Li
Youji He
Jianqiong Zhang
Gaojun Teng
机构
[1] Key Laboratory of Developmental Genes and Human Disease,Department of Pathology, Medical School
[2] Ministry of Education; Department of Microbiology and Immunology,undefined
[3] Medical School Southeast University,undefined
[4] Southeast University,undefined
[5] Jiangsu Key Laboratory of Molecular and Functional Imaging,undefined
[6] Department of Radiology,undefined
[7] Zhongda Hospital,undefined
[8] Medical School of Southeast University,undefined
来源
Biotechnology Letters | 2014年 / 36卷
关键词
Brain metastatic breast cancer; Cancer cells; Human brain-seeking breast carcinoma cells; Peptide; Phage display; Tumor targeting;
D O I
暂无
中图分类号
学科分类号
摘要
A novel peptide, BRBP1 (MYPWTEPSYLSN), was identified using an in vitro phage biopanning strategy against human brain-seeking breast carcinoma cells (231-BR cells).The peptide-phage clone, BRBP1-M13 displaying BRBP1 sequence, specifically bound to 231-BR cells and the binding could be competitively abolished by BRBP1. In vivo distribution studies showed that BRBP1-M13 preferentially homed to the 231-BR tumors. Fluorescently-labeled BRBP1, BRBP1-K(5-TAMRA), preferentially bound to 231-BR cells in a dose-dependent and energy-dependent manner and it was efficiently internalized into the cells after 2 h incubation. Near-infrared fluorophores imaging demonstrated the accumulation of Cy5.5-conjugated BRBP1 peptide in the tumors in vivo. Thus, BRBP1 is a promising peptide binding to human brain metastatic breast cancer and it may be applied to targeted delivery of cytotoxic agents to the intended tumor.
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页码:2291 / 2301
页数:10
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