Tracing Size and Surface Chemistry-Dependent Endosomal Uptake of Gold Nanoparticles Using Surface-Enhanced Raman Scattering

被引:12
|
作者
Ortas, Deniz Yasar [1 ]
Altunbek, Mine [1 ]
Uzunoglu, Deniz [1 ]
Yilmaz, Hulya [1 ]
Cetin, Demet [2 ]
Suludere, Zekiye [3 ]
Culha, Mustafa [1 ]
机构
[1] Yeditepe Univ, Fac Engn, Dept Genet & Bioengn, TR-34755 Istanbul, Turkey
[2] Gazi Univ, Gazi Fac Educ, Dept Math & Sci Educ, TR-06500 Ankara, Turkey
[3] Gazi Univ, Fac Sci, Dept Biol, TR-06500 Ankara, Turkey
关键词
SINGLE LIVING CELLS; LIVE CELLS; SPECTROSCOPY; FIXATION; SILVER; SHAPE;
D O I
10.1021/acs.langmuir.8b03988
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surface-enhanced Raman scattering (SERS)-based single-cell analysis is an emerging approach to obtain molecular level information from molecular dynamics in living cell. In this study, endosomal biochemical dynamics was investigated based on size and surface chemistry-dependent uptake of gold nanoparticles (AuNPs) on single cells over time using SERS. MDA-MB-231 breast cancer cells were exposed to 13 and 50 nm AuNPs and their polyadenine oligonucleotide-modified forms by controlling the order and combination of AuNPs. The average spectra obtained from 20 single cells were analyzed to study the nature of the biochemical species or processes taking place on the AuNP surfaces. The spectral changes, especially from proteins and lipids of endosomal vesicles, were observed depending on the size, surface chemistry, and combination as well as the duration of the AuNP treatment. The results demonstrate that SERS spectra are sensitive to trace biochemical changes not only the size, surface chemistry, and aggregation status of AuNPs but also the endosomal maturation steps over time, which can be simple and fast way for understanding the AuNP behavior in single cell and useful for the assisting and controlling of AuNP-based gene or drug delivery applications.
引用
收藏
页码:4020 / 4028
页数:9
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