Phan A T, Leroy J L, Guéron M
Groupe de biophysique de l'Ecole polytechnique et de l'UMR 7643 du CNRS, Ecole Polytechnique, Palaiseau, 91128, France.
J Mol Biol. 1999 Feb 19;286(2):505-19. doi: 10.1006/jmbi.1998.2467.
The residence time of water in the minor groove of the d(CGCGAATTCGCG) duplex has been determined by a recent measurement combining nuclear Overhauser enhancements (NOE, ROE) and 17O relaxation dispersion. The time is in the range of nanoseconds, so that it may be measured by a rather simple method proposed here, namely the choice of conditions such that the NOE between the observed DNA proton and a nearby water proton is zero. This condition is realized when the residence time of the water molecule is 0.178 times the nuclear magnetic resonance period (e.g. 0.297 ns at 600 MHz). It may be achieved by varying the magnetic field and/or the temperature. The zero-NOE measurement may be performed by one-dimensional NMR, and has therefore good sensitivity. We have developed excitation sequences which suppress two spurious contributions to the NOE: from neighboring exchangeable protons and from H3' protons whose chemical shift is close to that of water. The method is applied here to the comparison of residence times of water next to B-DNA and next to B'-DNA, the latter corresponding to better stacked, propeller-twisted base-pairs and a correspondingly narrower minor groove. In the minor groove of [d(CGCGAATTCGCG)]2, a B'-DNA duplex, the residence time of the water molecule next to H2 of adenine(6) (underlined), is 0.6 ns at 10 degreesC, in good agreement with the value obtained previously. The residence time is slightly but distinctly shorter for the water next to A5, suggesting non-cooperative departure of these two molecules which are presumed to be part of the hydration spine. Near A5 and A4 of [d(AAAAATTTTT)]2, another B'-DNA duplex, the residence times are approximately twice as long, but the activation enthalpies are about the same, ca. 38 kJ/mol. The residence time in the minor groove of the regular B-DNA sequence d(CGCGATCGCG) was 0.3 ns at 10 degreesC, shorter than in the case of the B'-DNA sequences by factors of 2 and 4, respectively. The temperature dependence is less, with an activation enthalpy of 27 kJ/mol. The major groove residence times are comparable for the three sequences, and a few times shorter than those of minor groove water. A value of 0.36 ns, or even more in case of rotation of water, is obtained around -8 degreesC. The most striking aspect of these results is the relatively small difference in the residence times of reputedly fast and slow-exchanging water molecules bound to DNA in biological conditions. This suggests that the spine of hydration is perhaps not a major stabilizer of the B'-DNA structure as compared with B-DNA.
通过最近一项结合核Overhauser增强效应(NOE、ROE)和17O弛豫色散的测量,已确定了水在d(CGCGAATTCGCG)双链体小沟中的停留时间。该时间处于纳秒范围,因此可以通过这里提出的一种相当简单的方法来测量,即选择这样的条件,使得观察到的DNA质子与附近水质子之间的NOE为零。当水分子的停留时间为核磁共振周期的0.178倍时(例如在600 MHz下为0.297 ns),该条件得以实现。这可以通过改变磁场和/或温度来实现。零NOE测量可以通过一维核磁共振进行,因此具有良好的灵敏度。我们已经开发出激发序列,可抑制对NOE的两种虚假贡献:来自相邻可交换质子以及化学位移与水接近的H3'质子。这里将该方法应用于比较B - DNA和B'- DNA旁边水的停留时间,后者对应于堆积更好、具有螺旋桨扭曲的碱基对以及相应更窄的小沟。在B'- DNA双链体[d(CGCGAATTCGCG)]2的小沟中,腺嘌呤(6)(下划线)的H2旁边水分子在10℃时的停留时间为0.6 ns,与先前获得的值吻合良好。A5旁边水的停留时间略短但明显缩短,这表明这两个被认为是水合脊柱一部分的分子的非协同离去。在另一个B'- DNA双链体[d(AAAAATTTTT)]2的A5和A4附近,停留时间大约是两倍长,但活化焓大致相同,约为38 kJ/mol。规则B - DNA序列d(CGCGATCGCG)在小沟中的停留时间在10℃时为0.3 ns,分别比B'- DNA序列的情况短2倍和4倍。温度依赖性较小,活化焓为27 kJ/mol。这三个序列在大沟中的停留时间相当,并且比小沟水的停留时间短几倍。在 - 8℃左右,得到的值为0.36 ns,若水发生旋转则甚至更高。这些结果最显著的方面是,在生物条件下与DNA结合的所谓快速和慢速交换水分子的停留时间差异相对较小。这表明与B - DNA相比,水合脊柱可能不是B'- DNA结构的主要稳定剂。