DNA-binding affinities and sequence selectivity of quaternary benzophenanthridine alkaloids sanguinarine, chelerythrine, and nitidine

被引:88
作者
Bai, Li-Ping
Zhao, Zhong-Zhen
Cai, Zongwei
Jiang, Zhi-Hong [1 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Baptist Univ, Dept Chem, Kowloon, Hong Kong, Peoples R China
关键词
alkaloid; DNA-binding; intercalations; fluorescence spectrometry; sequence selectivity;
D O I
10.1016/j.bmc.2006.05.012
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
A comparative study on the intercalating binding of sanguinarine, chelerythrine, and nitidine with CT DNA, poly(dG-dC)(.)poly(dG-dC), poly(dA-dT)(.)poly(dA-dT), and seven sequence-designed double-stranded oligodeoxynucleotides has been performed using fluorometric and spectrophotometric techniques, aiming at providing insights into their sequence selectivity for DNA-binding. The results show that both sanguinarine and nitidine bind preferentially to DNA containing alternating GC base pairs [d(TGCGCA)(2)], while chelerythrine exhibits quite distinct sequence selectivity from sanguinarine, which shows a high specificity for DNA containing contiguous GC base pairs [5 '-TGGGGA-3 '/3 '-ACCCCT-5 ']. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5439 / 5445
页数:7
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