Interactions of cryptolepine and neocryptolepine with unusual DNA structures

被引:136
作者
Guittat, L
Alberti, P
Rosu, F
Van Miert, S
Thetiot, E
Pieters, L
Gabelica, V
De Pauw, E
Ottaviani, A
Riou, JF
Mergny, JL
机构
[1] CNRS, INSERM, UMR 8646, UR 565,Museum Natl Hist Nat,Lab Biophys, F-75231 Paris 5, France
[2] Univ Liege, Chem Inst B6c, Biospect Lab, B-4000 Liege, Sart Tilman, Belgium
[3] Univ Instelling Antwerp, Dept Pharmaceut Sci, B-2610 Antwerp, Belgium
[4] Univ Liege, Dept Chem, Mass Spectrometry Lab, Liege, Belgium
[5] Univ Reims, UFR Pharm, Lab Physiol Humaine, F-51096 Reims, France
关键词
cryptolepine; triplex; quadruplex; telomere; telomerase; DOUBLE-STRANDED OLIGODEOXYNUCLEOTIDES; IONIZATION MASS-SPECTROMETRY; TRIPLE HELIX FORMATION; G-QUARTET FORMATION; G-QUADRUPLEX DNA; NONCOVALENT COMPLEXES; TELOMERASE INHIBITORS; TOPOISOMERASE-II; SEQUENCE; BINDING;
D O I
10.1016/S0300-9084(03)00035-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
Cryptolepine, the main alkaloid present in the roots of Cryptolepis sanguinolenta, presents a large spectrum of biological properties. It has been reported to behave like a DNA intercalator with a preference for GC-rich sequences. In this study, dialysis competition assay and mass spectrometry experiments were used to determine the affinity of cryptolepine and neocryptolepine for DNA structures among duplexes, triplexes, quadruplexes and single strands. Our data confirm that cryptolepine and neocryptolepine prefer GC over AT-rich duplex sequences, but also recognize triplex and quadruplex structures. These compounds are weak telomerase inhibitors and exhibit a significant preference for triplexes over quadruplexes or duplexes. (C) 2003 Editions scientifiques et medicales Elsevier SAS and Societe francaise de biochimie et biologic moleculaire. All rights reserved.
引用
收藏
页码:535 / 547
页数:13
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