Faltynek C R, Silbert J E, Hof L
J Biol Chem. 1981 Jul 25;256(14):7139-41.
Sugar nucleotide degradation by Zn2+-requiring nucleotide pyrophosphatase and phosphatase was effectively inhibited by the addition of the chelator 2,3-dimercaptopropan-1-ol, along with low concentrations of nucleotides or their analogues. The addition of dimercaptopropanol alone completely inhibited alkaline phosphatase. This chelator has a much higher association constant for Zn2+ than for the Mn2+ needed for glycosyltransferase reactions, enabling selective chelation of Zn2+. Neither the chelator alone nor in combination with low concentrations of nucleotides was inhibitory to glycosyltransferase activities, as shown by xylosyltransferase in chick embryo epiphyseal microsomes and galactosyltransferase in rat serum.
通过添加螯合剂2,3-二巯基丙醇以及低浓度的核苷酸或其类似物,可有效抑制由需要锌离子的核苷酸焦磷酸酶和磷酸酶介导的糖核苷酸降解。单独添加二巯基丙醇可完全抑制碱性磷酸酶。该螯合剂对锌离子的缔合常数比对糖基转移酶反应所需的锰离子的缔合常数高得多,从而能够选择性螯合锌离子。如鸡胚骨骺微粒体中的木糖基转移酶和大鼠血清中的半乳糖基转移酶所示,单独的螯合剂或与低浓度核苷酸组合使用时,均不会抑制糖基转移酶活性。