Livolant F, Maestre M F
Centre de Biologie Cellulaire, CNRS, Ivry-sur-Seine, France.
Biochemistry. 1988 Apr 19;27(8):3056-68. doi: 10.1021/bi00408a058.
Two highly condensed structures of DNA have been analyzed in the circular dichroism (CD) microscope: the cholesteric liquid-crystalline phase of DNA and the nucleus of a dinoflagellate (Prorocentrum micans). In both cases, the DNA shows a helical cholesteric organization, but the helical pitch equals about 2500 nm in the first case and 250 nm in the second one. Since the absorption band of DNA is located at 260 nm, the reflection and absorption bands are well separated in the cholesteric phase of DNA and are overlapping in the dinoflagellate nucleus. However, both structures give a very strong negative CD signal at 265 nm. We show that this very strong signal cannot correspond to a Borrmann effect, i.e., to a superposition of the absorption and reflection bands, but is a differential absorption of left versus right circularly polarized light. This anomalous differential absorption is probably due to a significant scattering of light, inside of the structure, which produces a resonance phenomenon in the absorption band of the chromophore. Therefore, for any helical structure containing a chromophore, the apparent CD can be expressed as CD = [(epsilon L - epsilon R)cl] + (psi L - psi R) + (SL - SR) The first term is true absorption and is located in the absorption band of the chromophore, and the last term is true scattering and is observed at the wavelength corresponding to the helical pitch of the structure. The second term (psi L - psi R) corresponds to the anomalous differential absorption observed in dense superhelical structures of DNA. It superimposes to the first term in the absorption band of the chromophore. psi L - psi R is a measure of the perfection of the helical structure and of the density of chromophores in the material. Intercalative dyes [ethidium bromide and meso-tetrakis(4-N-methylpyridyl)porphine (H2TMpyP-4) and its nickel(II) derivative (NiIITMpyP-4)] were inserted in the dinoflagellate chromatin. The CD signal recorded in their absorption band mimics the signal observed in the absorption band of DNA. In both structures, the negative sign of the CD at 265 nm indicates that the twist occurring between DNA. In both structures, the negative sign of the CD at 265 nm indicates that the twist occurring between DNA molecules is left-handed, and we show that this situation is the most frequently encountered in vivo and vitro.
利用圆二色性(CD)显微镜分析了DNA的两种高度凝聚结构:DNA的胆甾相液晶相和一种甲藻(海洋原甲藻)的细胞核。在这两种情况下,DNA均呈现螺旋状胆甾型结构,但第一种情况下螺旋间距约为2500 nm,第二种情况下为250 nm。由于DNA的吸收带位于260 nm处,因此在DNA的胆甾相中介电反射带和吸收带是分开的,而在甲藻细胞核中二者是重叠的。然而,两种结构在265 nm处均给出非常强的负CD信号。我们表明,这种非常强的信号并非对应于玻恩效应,即吸收带和反射带的叠加,而是左旋与右旋圆偏振光的差分吸收。这种异常的差分吸收可能是由于结构内部光的显著散射,从而在发色团的吸收带中产生共振现象。因此,对于任何含有发色团的螺旋结构,表观CD可表示为CD = [(εL - εR)cl] + (ψL - ψR) + (SL - SR)。第一项是真实吸收,位于发色团的吸收带中,最后一项是真实散射,在与结构螺旋间距对应的波长处观察到。第二项(ψL - ψR)对应于在DNA致密超螺旋结构中观察到的异常差分吸收。它在发色团的吸收带中叠加到第一项上。ψL - ψR是螺旋结构完善程度以及材料中发色团密度的一种度量。插入性染料[溴化乙锭、中位四(4 - N - 甲基吡啶基)卟啉(H2TMpyP - 4)及其镍(II)衍生物(NiIITMpyP - 4)]被插入到甲藻染色质中。在其吸收带记录的CD信号模拟了在DNA吸收带中观察到的信号。在两种结构中,265 nm处CD的负号表明DNA分子之间发生的扭曲是左旋的,并且我们表明这种情况在体内和体外最为常见。