DOX-DNA Interactions on the Nanoscale: In Situ Studies Using Tip-Enhanced Raman Scattering

被引:2
作者
Majzner, Katarzyna [1 ]
Deckert-Gaudig, Tanja [2 ,3 ,4 ]
Baranska, Malgorzata [1 ,5 ]
Deckert, Volker [2 ,3 ,4 ]
机构
[1] Jagiellonian Univ, Fac Chem, Dept Chem Phys, PL-30387 Krakow, Poland
[2] Friedrich Schiller Univ Jena, Inst Phys Chem, D-07743 Jena, Germany
[3] Abbe Ctr Photon, Helmholtzweg 4, D-07743 Jena, Germany
[4] Leibniz Inst Photon Technol, D-07745 Jena, Germany
[5] Jagiellonian Univ, Jagiellonian Ctr Exper Imental Therapeut JCET, PL-30348 Krakow, Poland
关键词
RESONANCE RAMAN; SINGLE-MOLECULE; SPECTROSCOPY; DOXORUBICIN; SERS; ADRIAMYCIN; SPECTRA; ANTHRACYCLINES; RESOLUTION; COMPLEXES;
D O I
10.1021/acs.analchem.3c05372
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chemotherapeutic anthracyclines, like doxorubicin (DOX), are drugs endowed with cytostatic activity and are widely used in antitumor therapy. Their molecular mechanism of action involves the formation of a stable anthracycline-DNA complex, which prevents cell division and results in cell death. It is known that elevated DOX concentrations induce DNA chain loops and overlaps. Here, for the first time, tip-enhanced Raman scattering was used to identify and localize intercalated DOX in isolated double-stranded calf thymus DNA, and the correlated near-field spectroscopic and morphologic experiments locate the DOX molecules in the DNA and provide further information regarding specific DOX-nucleobase interactions. Thus, the study provides a tool specifically for identifying intercalation markers and generally analyzing drug-DNA interactions. The structure of such complexes down to the molecular level provides mechanistic information about cytotoxicity and the development of potential anticancer drugs.
引用
收藏
页码:8905 / 8913
页数:9
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