Nile Red nucleoside: Design of a solvatofluorochromic nucleoside as an indicator of micropolarity around DNA

被引:63
作者
Okamoto, A [1 ]
Tainaka, K [1 ]
Fujiwara, Y [1 ]
机构
[1] Kyoto Univ, Fac Engn, Dept Synth Chem & Biol Chem, Kyoto 6158510, Japan
关键词
D O I
10.1021/jo060168o
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The fluorophore, Nile Red, effectively works as a polarity-sensitive fluorescence probe. We have designed a new nucleoside modified by Nile Red for examining the change in the polarity of the microenvironment surrounding DNA. We synthesized a Nile Red nucleoside (1), formed by replacing nucleobases with Nile Red, through the coupling of a 2-hydroxylated Nile Red derivative and 1,2-dideoxyglycan. This nucleoside showed a high solvatofluorochromicity. The fluorescence of 1 incorporated into DNA was greatly shifted to shorter wavelength by the addition of beta-cyclodextrin. The photophysical function of the Nile Red nucleoside will be a good optical indicator for monitoring the change in the micropolarity properties at a specific site on target sequences with interaction between DNA and DNA-binding molecules.
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收藏
页码:3592 / 3598
页数:7
相关论文
共 38 条
[31]  
2-4
[32]   Enhancement of excited state nonradiative deactivation of Nile Red in γ-cyclodextrin:: evidence for multiple inclusion complexes [J].
Srivatsavoy, VJP .
JOURNAL OF LUMINESCENCE, 1999, 82 (01) :17-23
[33]  
Strässler C, 1999, HELV CHIM ACTA, V82, P2160, DOI 10.1002/(SICI)1522-2675(19991215)82:12<2160::AID-HLCA2160>3.0.CO
[34]  
2-4
[35]   Introduction and general overview of cyclodextrin chemistry [J].
Szejtli, J .
CHEMICAL REVIEWS, 1998, 98 (05) :1743-1753
[36]   Probing zeolites with organic molecules: Supercages of X and Y zeolites are superpolar [J].
Uppili, S ;
Thomas, KJ ;
Crompton, EM ;
Ramamurthy, V .
LANGMUIR, 2000, 16 (01) :265-274
[37]  
WARD DC, 1969, J BIOL CHEM, V244, P1228
[38]  
Wojczewski C, 1999, SYNLETT, P1667