Muntean C M, Puppels G J, Greve J, Segers-Nolten G M J
National Institute for Research and Development of Isotopic and Molecular Technologies, P.O. 5, Box 700, R-3400 Cluj-Napoca, Romania.
Biopolymers. 2002;67(4-5):282-4. doi: 10.1002/bip.10116.
A confocal Raman microspectrometer was used to investigate the influence of Ca2+ cations on low pH-induced DNA structural changes. The effects of Ca2+ cations on the protonation mechanism of opening AT and changing the protonation of GC base pairs in DNA are discussed. Based on the observation that the midpoint of the transition of Watson-Crick GC base pairs to protonated GC base pairs lies at around pH 3 (analyzing the 681 cm(-1) line), measurements were carried out on calf thymus DNA at neutral pH and pH 3 in the presence of low and high concentrations of Ca2+ cations. Raman spectra show that low concentrations of Ca2+ cations partially protect DNA against protonation of cytosine (characteristic line at 1262 cm(-1)) and do not protect adenine (characteristic line at 1304 cm(-1)) and the N(7) of guanine (line at 1488 cm(-1)) against binding of H+. High Ca2+ concentrations can prevent protonation of cytosine and protonation of adenine (little disruption of AT pairs). Analyzing the line at 1488 cm(-1), which obtains most of its intensity from a guanine vibration, high salt was also found to protect the N(7) of guanine against protonation.
使用共聚焦拉曼光谱仪研究Ca2+阳离子对低pH诱导的DNA结构变化的影响。讨论了Ca2+阳离子对DNA中AT碱基对打开的质子化机制以及GC碱基对质子化变化的影响。基于观察到沃森-克里克GC碱基对向质子化GC碱基对转变的中点位于pH 3左右(分析681 cm(-1)谱线),在低浓度和高浓度Ca2+阳离子存在的情况下,在中性pH和pH 3条件下对小牛胸腺DNA进行了测量。拉曼光谱表明,低浓度的Ca2+阳离子部分保护DNA免受胞嘧啶质子化(1262 cm(-1)处的特征谱线)影响,但不能保护腺嘌呤(1304 cm(-1)处的特征谱线)和鸟嘌呤的N(7)(1488 cm(-1)处的谱线)免受H+结合的影响。高浓度的Ca2+可以防止胞嘧啶的质子化和腺嘌呤的质子化(对AT碱基对的破坏较小)。分析1488 cm(-1)处的谱线(其大部分强度来自鸟嘌呤振动),还发现高盐可以保护鸟嘌呤的N(7)免受质子化。