Department of Spectroscopy, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, India.
J Phys Chem B. 2012 May 3;116(17):5226-33. doi: 10.1021/jp301211m. Epub 2012 Apr 24.
This paper reports an interesting transformation of binding mode of 2-(4-(dimethylamino)styryl)-1-methylpyridinium iodide (DASPMI) with calf thymus DNA from minor groove binding in buffer solution to intercalative binding when the dye is encapsulated inside a vesicle formed by the interaction of 1,8-naphthalimide (a charge transfer dye) with the supramolecular association of sodium dodecyl sulfate and block-copolymer polyethylene-b-polyethylene glycol. The pre-encapsulated dye in the vesicular interior binds intercalatively to ct-DNA, as evinced by the high value of equilibrium binding constant of DASPMI-DNA complex, changes in CD-spectra of DNA and isosbestic point, along with downshift and hypochromicity of absorption band. Increase in anisotropy decay by 1.5 times with a single component strongly confirms restricted motion of the probe inside ct-DNA confirming intercalative binding. The compaction of ct-DNA caused by the interaction of the vesicle allows DASPMI to bind ct-DNA in the intercalative mode. However, the groove binding mode in ct-DNA-DASPMI remains unaffected by the retro-addition of the vesicles to the already bound dye to ct-DNA.
本文报道了一种有趣的 2-(4-(二甲基氨基)苯乙烯基)-1-甲基吡啶翁碘化物(DASPMI)与小牛胸腺 DNA 结合模式的转变,即在缓冲溶液中从较小的沟结合转变为当染料被包裹在由 1,8-萘二甲酰亚胺(一种电荷转移染料)与十二烷基硫酸钠和嵌段共聚物聚乙二醇的超分子缔合相互作用形成的囊泡内时的插入结合。预封装在囊泡内部的染料与 ct-DNA 进行插入结合,这可以通过 DASPMI-DNA 复合物的平衡结合常数、DNA 的 CD 光谱变化和等色点以及吸收带的蓝移和减色性来证明。各向异性衰减增加了 1.5 倍,只有一个分量,这强烈证实了探针在 ct-DNA 内的受限运动,证实了插入结合。囊泡的相互作用引起的 ct-DNA 的紧缩允许 DASPMI 以插入结合的方式与 ct-DNA 结合。然而,囊泡的再加入对已经与 ct-DNA 结合的染料的 ct-DNA-DASPMI 的沟结合模式没有影响。