Monnot M, Mauffret O, Simon V, Lescot E, Psaume B, Saucier J M, Belehradek J, Fermandjian S
Institut Gustave Roussy, PRII, Laboratoire de Biochimie-Enzymologie, URA147 CNRS, U140 INSERM, Villejuif, France.
FEBS Lett. 1990 Oct 29;273(1-2):71-4. doi: 10.1016/0014-5793(90)81053-q.
UV-absorption and circular dichroism (CD) experiments showed that ellipticine derivatives may interact with DNA according to 3 possible binding modes depending on their structure and concentration. The first mode concerned intercalation of 1-methyl-9-hydroxyellipticine (1-Me-HE) with its long axis perpendicular to the long axis of base pairs. The same drug was able to bind to external sites (second mode) once the intercalation sites were saturated at high concentration. The third mode illustrated by 1,2-dimethyl-9-hydroxyisoellipticinium (1-Me-isoNMHE), concerned self-stacked molecules interacting at the surface of DNA. Biological significance of these different binding modes was then discussed in connection with in vitro cytotoxic activity of compounds.
紫外吸收和圆二色性(CD)实验表明,根据其结构和浓度,椭圆玫瑰树碱衍生物可能通过三种可能的结合模式与DNA相互作用。第一种模式涉及1-甲基-9-羟基椭圆玫瑰树碱(1-Me-HE)的嵌入,其长轴垂直于碱基对的长轴。一旦在高浓度下嵌入位点饱和,相同的药物能够结合到外部位点(第二种模式)。由1,2-二甲基-9-羟基异椭圆玫瑰树碱(1-Me-isoNMHE)说明的第三种模式,涉及在DNA表面相互作用的自堆积分子。然后结合化合物的体外细胞毒性活性讨论了这些不同结合模式的生物学意义。