Aggregation of nanoparticles in endosomes and lysosomes produces surface-enhanced Raman spectroscopy

被引:9
|
作者
Lucas, Leanne J. [1 ]
Chen, Xiaoke K. [2 ]
Smith, Aaron J. [1 ]
Korbelik, Mladen [3 ]
Zeng, Haishan [3 ]
Lee, Patrick W. K. [4 ]
Hewitt, Kevin Cecil [1 ]
机构
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 4R2, Canada
[2] Simon Fraser Univ, Dept Phys, Burnaby, BC V5A 1S6, Canada
[3] British Columbia Canc Res Ctr, Imaging Unit, Vancouver, BC V5Z 1L3, Canada
[4] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3H 4R2, Canada
基金
加拿大创新基金会;
关键词
surface-enhanced Raman spectroscopy; epidermal growth factor receptor overexpression; gold nanoparticles; cancer imaging; endosomes; lysosomes; GROWTH-FACTOR RECEPTOR; EXPRESSION; SPECTRA;
D O I
10.1117/1.JNP.9.093094
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The purpose of this study was to explore the use of surface-enhanced Raman spectroscopy (SERS) to image the distribution of epidermal growth factor receptor (EGFR) in cells. To accomplish this task, 30-nm gold nanoparticles (AuNPs) tagged with antibodies to EGFR (10(12) per mL) were incubated with cells (10(6) per mL) of the A431 human epidermoid carcinoma and normal human bronchial epithelial cell lines. Using the 632.8-nm excitation line of a He-Ne laser, Raman spectroscopy measurements were performed using a point mapping scheme. Normal cells show little to no enhancement. SERS signals were observed inside the cytoplasm of A431 cells with an overall enhancement of 4 to 7 orders of magnitude. Raman intensity maps of the 1450 and 1583 cm(-1) peaks correlate well with the expected distribution of EGFR and AuNPs, aggregated following uptake by endosomes and lysosomes. Spectral features from tyrosine and tryptophan residues dominate the SERS signals. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License.
引用
收藏
页数:14
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