Hiwada K, Tokioka-Terao M, Nishimura K, Kokubu T
Clin Chem. 1984 Feb;30(2):222-5.
We found a family with a high activity for hydrolyzing L-alanyl-beta-naphthylamide in their serum. This enzyme was confirmed to be aminopeptidase (microsomal) (EC 3.4.11.2) by means of immunological experiments involving anti-human kidney aminopeptidase (microsomal) antibody. We could not find the cause of the increased activity from the results of clinical and laboratory examinations. The enzyme from the propositus resembled that from the serum of normal subjects in molecular mass (240 000 Da), Km value (87 mumol/L), and degree of inhibition by antiserum to human kidney aminopeptidase (microsomal). It differed from the normal enzyme with respect to electrophoretic mobility (R1 value, 0.58; normal, 0.51), isoelectric point (pI, pH 3.4; normal, pH 3.8), and heat stability (more labile than normal). From information on this family and another one reported in the Japanese literature, we suggest that the mode of inheritance of a high activity of serum aminopeptidase (microsomal) may be autosomal dominant.
我们发现一个家族,其血清中水解L-丙氨酰-β-萘酰胺的活性很高。通过使用抗人肾氨基肽酶(微粒体)抗体进行的免疫学实验,证实该酶为氨基肽酶(微粒体)(EC 3.4.11.2)。从临床和实验室检查结果中,我们找不到活性增加的原因。先证者的酶在分子量(240 000 Da)、Km值(87 μmol/L)以及抗人肾氨基肽酶(微粒体)抗血清的抑制程度方面,与正常受试者血清中的酶相似。在电泳迁移率(R1值,0.58;正常为0.51)、等电点(pI,pH 3.4;正常为pH 3.8)和热稳定性(比正常酶更不稳定)方面,它与正常酶不同。根据这个家族以及日本文献中报道的另一个家族的信息,我们认为血清氨基肽酶(微粒体)高活性的遗传方式可能是常染色体显性遗传。