Rubin J R, Sundaralingam M
Department of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison 53706.
J Biomol Struct Dyn. 1983 Dec;1(3):639-46. doi: 10.1080/07391102.1983.10507471.
Crystalline complexes of yeast phenylalanine tRNA and Lead (II) ion were prepared by soaking pregrown orthorhombic crystals of tRNA in saturated lead chloride solutions. The locations of tightly bound lead ions on the tRNA were determined by difference Fourier methods. There are three major lead binding sites; two of these replace tightly bound magnesium ions in the native tRNA structure. Site I is located in the dihydrouridine loop of the molecule adjacent to phosphate P18 which is specifically cleaved by lead. This is evident from changes observed in the Pb-native difference electron density maps. A possible mechanism for lead ion hydrolysis of the polynucleotide chain is proposed.
通过将预生长的正交晶系酵母苯丙氨酸tRNA晶体浸泡在饱和氯化铅溶液中,制备了酵母苯丙氨酸tRNA与铅(II)离子的晶体复合物。通过差值傅里叶方法确定了紧密结合在tRNA上的铅离子的位置。有三个主要的铅结合位点;其中两个取代了天然tRNA结构中紧密结合的镁离子。位点I位于分子的二氢尿嘧啶环中,与被铅特异性切割的磷酸P18相邻。这从铅-天然差值电子密度图中观察到的变化可以明显看出。提出了一种铅离子水解多核苷酸链的可能机制。