Weinfeld M, Liuzzi M, Paterson M C
Department of Medicine, Cross Cancer Institute, Edmonton, Alberta, Canada.
Nucleic Acids Res. 1989 May 25;17(10):3735-45. doi: 10.1093/nar/17.10.3735.
Partial depurination of d-ApA produced two UV260nm-absorbing isomers, d-SpA and d-ApS (where S represents the depurinated deoxyribose sugar), that provided simple model compounds with which to examine, by HPLC, the response of nucleases to phosphodiester bonds flanked 3' or 5' by an apurinic site. The structural identity of each compound was established by (i) reaction with methoxyamine to confirm the presence of an abasic deoxyribose group, and (ii) degradation of d-SpA under mild alkaline conditions to distinguish it from d-ApS. At an enzyme concentration which led to complete hydrolysis of d-ApA, snake venom phosphodiesterase readily cleaved d-SpA to 5'-dAMP but had no discernible effect on d-ApS. Calf spleen phosphodiesterase also failed to act on one isomer, in this instance d-SpA, but additionally reacted at a much slower rate (approximately 100 fold) with d-ApS than with d-ApA. Three single-strand specific endonucleases, nuclease P1, nuclease S1 and mung bean nuclease, all responded in an identical manner, hydrolysing d-ApS but not d-SpA. The possibility that the aldehyde group at the AP sites might be responsible for some of these observations was rejected after repeating the enzyme digestions with the methoxyamine-capped molecules and observing no differences from the reactions with d-SpA and d-ApS.
d - ApA的部分脱嘌呤作用产生了两种在260nm处有紫外吸收的异构体,d - SpA和d - ApS(其中S代表脱嘌呤的脱氧核糖),它们提供了简单的模型化合物,可用于通过高效液相色谱法研究核酸酶对嘌呤缺失位点3'或5'侧翼磷酸二酯键的反应。通过以下方法确定了每种化合物的结构特征:(i)与甲氧基胺反应以确认无碱基脱氧核糖基团的存在,以及(ii)在温和碱性条件下使d - SpA降解以将其与d - ApS区分开来。在导致d - ApA完全水解的酶浓度下,蛇毒磷酸二酯酶能轻易地将d - SpA切割成5'-dAMP,但对d - ApS没有明显作用。小牛脾磷酸二酯酶也对其中一种异构体(即d - SpA)不起作用,但此外,它与d - ApS的反应速率比与d - ApA的反应速率慢得多(约100倍)。三种单链特异性核酸内切酶,核酸酶P1、核酸酶S1和绿豆核酸酶,反应方式相同,均能水解d - ApS但不能水解d - SpA。在用甲氧基胺封端的分子重复酶消化实验并观察到与d - SpA和d - ApS反应无差异后,排除了AP位点的醛基可能导致这些观察结果的可能性。