Jamil T P, Swallow D M, Povey S
Biochem Genet. 1978 Dec;16(11-12):1219-32. doi: 10.1007/BF00484542.
The nucleoside monophosphate kinases, adenylate kinase (AK), guanylate kinase (GUK), and uridine monophosphate kinase (UMPK), were studied electrophoretically and quantitatively in density gradient fractions of human red cells from normal adults which contain red cells of differing mean age. The enzymes were found to differ both in their rates and patterns of decay and in secondary isozyme formation during the life of the red cell in the circulation. AK showed no appreciable enzyme decay and slight genetation of secondary isozymes; UMPK showed a rapid monophasic decline and no secondary isozyme formation; GUK showed intermediate overall loss of activity with a biphasic pattern of decay and marked secondary isozyme formation. A comparative study of the two common phenotypes of UMPK (UMPK 1 and UMPK 2-1) and of AK (AK 1 and AK 2-1) was made. The UMPK 2 isozyme showed a more rapid decay than the UMPK 1 isozyme, whereas no difference was observed between the AK 1 and AK 2 isozymes.
对核苷单磷酸激酶,即腺苷酸激酶(AK)、鸟苷酸激酶(GUK)和尿苷单磷酸激酶(UMPK),在来自正常成年人的人红细胞密度梯度组分中进行了电泳和定量研究,这些组分包含不同平均年龄的红细胞。发现这些酶在循环中红细胞寿命期间的衰减速率和模式以及二级同工酶形成方面均存在差异。AK没有明显的酶衰减,二级同工酶生成轻微;UMPK呈现快速单相下降且没有二级同工酶形成;GUK呈现中等程度的总体活性丧失,具有双相衰减模式和明显的二级同工酶形成。对UMPK的两种常见表型(UMPK 1和UMPK 2-1)以及AK的两种常见表型(AK 1和AK 2-1)进行了比较研究。UMPK 2同工酶的衰减比UMPK 1同工酶更快,而AK 1和AK 2同工酶之间未观察到差异。