Ahmad R, Naoui M, Neault J F, Diamantoglou S, Tajmir-Riahi H A
Departement Chimie-Biologie, Université du Québec à Trois-Rivières, Canada.
J Biomol Struct Dyn. 1996 Apr;13(5):795-802. doi: 10.1080/07391102.1996.10508892.
The interaction of calf-thymus DNA with trivalent Al and Ga cations, in aqueous solution at pH = 6-7 with cation/DNA(P) (P = phosphate) molar ratios (r) 1/80, 1/40, 1/20, 1/10, 1/4 and 1/2 was characterized by Fourier Transform infrared (FTIR) difference spectroscopy. Spectroscopic results show the formation of several types of cation-DNA complexes. At low metal ion concentration (r = 1/80, 1/40), both cations bind mainly to the backbone PO2 group and the guanine N-7 site of the G-C base pairs (chelation). Evidence for cation chelate formation comes from major shifting and intensity increase of the phosphate antisymmetric stretch at 1222 cm-1 and the mainly guanine band at 1717 cm-1. The perturbations of A-T base pairs occur at high cation concentration with major helix destabilization. Evidence for cation binding to A-T bases comes from major spectral changes of the bands at 1663 and 1609 cm-1 related mainly to the thymine and adenine in-plane vibrations. A major reduction of the B-DNA structure occurs in favor of A-DNA upon trivalent cation coordination.
在pH = 6 - 7的水溶液中,以阳离子/DNA(P)(P = 磷酸根)摩尔比(r)为1/80、1/40、1/20、1/10、1/4和1/2,通过傅里叶变换红外(FTIR)差示光谱对小牛胸腺DNA与三价铝和镓阳离子的相互作用进行了表征。光谱结果表明形成了几种类型的阳离子-DNA复合物。在低金属离子浓度(r = 1/80、1/40)下,两种阳离子主要与主链PO2基团以及G-C碱基对的鸟嘌呤N-7位点结合(螯合)。阳离子螯合物形成的证据来自于1222 cm-1处磷酸根反对称伸缩振动以及1717 cm-1处主要的鸟嘌呤谱带的主要位移和强度增加。在高阳离子浓度下会发生A-T碱基对的扰动,并伴有主要的螺旋不稳定。阳离子与A-T碱基结合的证据来自于1663和1609 cm-1处谱带的主要光谱变化,这些变化主要与胸腺嘧啶和腺嘌呤的面内振动有关。在三价阳离子配位后,B-DNA结构发生显著减少,有利于A-DNA的形成。