Fluorescence spectral properties of the anticancer drug topotecan by steady-state and frequency domain fluorometry with one-photon and multi-photon excitation

被引:22
作者
Gryczynski, I
Gryczynski, Z
Lakowicz, JR
Yang, DZ
Burke, TG
机构
[1] Univ Maryland, Sch Med, Dept Biochem & Mol Biol, Ctr Fluorescence Spect, Baltimore, MD 21201 USA
[2] Univ Kentucky, Lexington, KY USA
关键词
D O I
10.1111/j.1751-1097.1999.tb03307.x
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
Topotecan is an antitumor agent with activity against a variety of cancers. We examined the steady-state and time-resolved fluorescence spectral properties of topotecan with one- and two-photon excitation. Topotecan was found to display a high two-photon cross section near 20 GM for wavelengths within the fundamental output of a Ti:sapphire laser, 800-880 nm, In frozen solution the anisotropies of topotecan are near the theoretical maxima for one-photon and two-photon excitation with colinear electronic transitions. The intensity and anisotropy decays of topotecan fluorescence were found to be homogeneous (single exponentials) in phosphate-buffered saline and propylene glycol. The steady-state and time-resolved data indicate that topotecan binds to a double-helical DNA oligomer d(AT)(10) resulting in increased anisotropies and multiexponential intensity and anisotropy decays, Subnanosecond components in the anisotropy decay of the DNA-topotecan complex suggest loose binding of the drug to DNA, Loose binding of topotecan to DNA is also revealed by accessibility of topotecan to collisional quenching by iodide.
引用
收藏
页码:421 / 428
页数:8
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