Sunnerhagen M, Denisov V P, Venu K, Bonvin A M, Carey J, Halle B, Otting G
Department of Medical Biochemistry and Biophysics, Karolinska Institute, Doktorsringen 9A1, Stockholm, S-171 77, Sweden.
J Mol Biol. 1998 Oct 2;282(4):847-58. doi: 10.1006/jmbi.1998.2033.
The present NMR study investigates the residence times of the hydration water molecules associated with uncomplexed trp operator DNA in solution by measuring intermolecular nuclear Overhauser effects (NOE) between water and DNA protons, and the nuclear magnetic relaxation dispersion (NMRD) of the water 2H and 17O resonances. Both methods indicate that the hydration water molecules exchange with bulk water on the sub-nanosecond time scale at 4 degreesC. No evidence was obtained for water molecules bound with longer residence times. In particular, the water molecules at the sites of interfacial hydration in the trp repressor/operator complex do not seem kinetically stabilized in the uncomplexed DNA. Analysis of the crystal structures of two different trp repressor/operator complexes shows very similar structural environments for the water molecules mediating specific contacts between the protein and the DNA, whereas much larger variations are observed for the location of corresponding water molecules detected in the crystal structure of an uncomplexed trp operator DNA duplex. Therefore, it appears unlikely that the hydration characteristics of the uncomplexed DNA target would be a major determinant of trp repressor/operator recognition.
目前的核磁共振研究通过测量水与DNA质子之间的分子间核Overhauser效应(NOE)以及水的2H和17O共振的核磁共振弛豫色散(NMRD),来研究溶液中与未复合的色氨酸操纵子DNA相关的水合水分子的停留时间。两种方法均表明,在4℃时,水合水分子在亚纳秒时间尺度上与大量水发生交换。没有获得停留时间更长的结合水分子的证据。特别是,色氨酸阻遏物/操纵子复合物中界面水合位点处的水分子在未复合的DNA中似乎没有动力学上的稳定。对两种不同的色氨酸阻遏物/操纵子复合物晶体结构的分析表明,介导蛋白质与DNA之间特异性接触的水分子的结构环境非常相似,而在未复合的色氨酸操纵子DNA双链体晶体结构中检测到的相应水分子的位置则观察到更大的变化。因此,未复合的DNA靶标的水合特性似乎不太可能是色氨酸阻遏物/操纵子识别的主要决定因素。