Butzow J J, Eichhorn G L
J Inorg Biochem. 1986 Sep;28(1):21-31. doi: 10.1016/0162-0134(86)80020-4.
The conditions under which Pb(II) promotes dephosphorylation of nucleotides have been studied with the Pb(II) complexes of several isomers of AMP, dAMP, GMP, and dGMP. A number of factors which together control the dephosphorylation reaction have been identified. These include the tendency of Pb(II)-induced nucleotide base stacking, as evidenced by large enhancement in ultraviolet circular dichroism, to occur in the complexes and limit the reaction; hydroxylation of the metal, either with weakening of the lead-nucleotide binding, or eventually with displacement of the nucleotide; and the solubility of the complexes, which limits the reaction, but is increased by raising the temperature and by hydroxylation of the complexes. The pH range in which both base stacking and metal hydrolysis are minimized can define a "reaction window" for the complexes.
通过研究AMP、dAMP、GMP和dGMP的几种异构体与Pb(II)形成的配合物,探讨了Pb(II)促进核苷酸去磷酸化的条件。已确定了一些共同控制去磷酸化反应的因素。这些因素包括:Pb(II)诱导的核苷酸碱基堆积倾向,这在紫外圆二色性中表现为大幅增强,该倾向在配合物中发生并限制反应;金属的羟基化,这要么会削弱铅 - 核苷酸结合,要么最终导致核苷酸被取代;配合物的溶解度,它限制了反应,但通过升高温度和配合物的羟基化作用而增加。碱基堆积和金属水解均最小化的pH范围可以为这些配合物定义一个“反应窗口”。