Small-Protein-Stabilized Semiconductor Nanoprobe for Targeted Imaging of Cancer Cells

被引:10
作者
Zhao, Ning [1 ]
Liu, Siyu [1 ]
Jiang, Qike [2 ]
Lan, Tian [1 ]
Cheng, Zhen [3 ]
Liu, Hongguang [1 ]
机构
[1] Northeastern Univ, Inst Mol Med, Coll Life & Hlth Sci, 195 Chuangxin Rd, Shenyang 110000, Japan
[2] Chinese Acad Sci, Dalian Inst Chem Phys, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[3] Stanford Univ, Dept Radiol, Mol Imaging Program Stanford, 1201 Welch Rd, Stanford, CA 94040 USA
关键词
Affibody; HER2; fluorescent imaging; one-pot synthesis; quantum dots; QUANTUM DOTS; BREAST-CANCER; ANTI-HER2; ANTIBODY; IN-VIVO; NANOPARTICLES; TUMORS; HER2; LUNG; PET;
D O I
10.1002/cbic.201600219
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, semiconductor nanoparticles such as quantum dots (QDs) have attracted significant attention for bioimaging. Complex chemical functionalization, surface modification, and bioconjugation chemistry are generally required to tag biomolecules to QDs for imaging of different biomarkers. In this study, we report a simple method for production of QDs stabilized by the small protein, Affibody (AF-QDs) for fluorescent imaging of the human epidermal growth factor receptor type2 (HER2) in human A549 lung cancer cells. This one-pot synthesis of AF-QDs avoids complex chemical conjugation procedures and demonstrates a promising approach for the preparation of fluorescent nanoprobes for imaging of cancer targets.
引用
收藏
页码:1202 / 1206
页数:5
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