体内
肽
SKBR3型
体外
癌症研究
磁小体
化学
材料科学
生物
生物化学
癌症
癌细胞
冶金
生物技术
磁铁矿
遗传学
人体乳房
作者
Zhichu Xiang,Xiaoliang Yang,Junjie Xu,Wenjia Lai,Zihua Wang,Zhiyuan Hu,Jiesheng Tian,Lingling Geng,Qiaojun Fang
出处
期刊:Biomaterials
[Elsevier]
日期:2016-11-17
卷期号:115: 53-64
被引量:79
标识
DOI:10.1016/j.biomaterials.2016.11.022
摘要
A novel peptide (P75) targeting EGFR and HER2 is successfully screened from a one-bead-one-compound (OBOC) library containing approximately 2 × 105 peptides built with the aid of computational simulation. In vitro and in vivo analyses show that P75 binds to human epithelial growth factor receptor (EGFR) with nanomolar affinity and to epithelial growth factor receptor-2 (HER2) with a lower affinity but comparable to other reported peptides. The peptide is used to modify the surface of magnetosome nanoparticles (NPs) for targeted magnetic resonance imaging (MRI). In vitro and in vivo fluorescence imaging results suggest peptide P75 modified magnetosomes (Mag-P75) specifically bind to MDA-MB-468 and SKBR3 cells as well as xenograft tumors with surprisingly low accumulation in other organs including liver and kidney. In vivo T2-weighted MR imaging studies of the xenograft tumors from SKBR3 and MDA-MB-468 cells show obviously negative contrast enhancement. The high affinity and specificity of P75 to EGFR and HER2 positive tumors, together with the success of peptide functionalized magnetosome NPs for targeted MRI demonstrate the potential of this peptide being used in the EGFR and HER2 positive tumors diagnosis and therapy.
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