Suppr超能文献

鸟类和人类腺苷脱氨酶同工酶的比较及可能的同源性

Comparison and possible homology of isozymes of adenosine deaminase in Aves and humans.

作者信息

Ratech H, Thorbecke G J, Meredith G, Hirschhorn R

出版信息

Enzyme. 1981;26(2):74-84. doi: 10.1159/000459153.

Abstract

Two kinetically distinct adenosine deaminase (ADA) isozymes with different molecular weights (35,000 and 100,000 daltons) are found in chicken liver in approximately equal amounts. The 100,000-dalton ADA has a markedly higher Km for adenosine and a markedly lower deaminating activity for deoxyadenosine relative to adenosine than does the 35,000-dalton ADA. A 100,000-dalton ADA isozyme has only recently been detected in mammalian tissues, where, in contrast to the chicken, it is only a trace component of total ADA activity. The human 100,000-dalton ADA isozyme, compared to the human 35,000-dalton ADA isozyme, has been reported to have a higher Km, a lower pH optimum, and a greater resistance to inhibition by erythro-9-(2-hydroxy-2-nonyl) adenine (EHNA). The similarity in KmS of the 100,000-dalton ADA isozyme in man and aves led us to hypothesize that these isozymes might be descended from a common ancestor and therefore also be similar as to other kinetic parameters. We now report that the chicken 100,000-dalton ADA, like the human 100,000-dalton isozyme, has a lower pH optimum and a greater resistance to inhibition by EHNA than does the avian or human 35,000-dalton isozyme. In addition, the avian 100,000-dalton isozyme is relatively resistant to inhibition by deoxycoformycin and has a cathodal rather than an anodal electrophoretic mobility at pH 6.5. Conversely, we report that the human 100,000-dalton ADA isozyme, similar to the avian 100,000-dalton ADA, has markedly lower relative deaminating activity for deoxyadenosine than does the 35,000-dalton ADA human isozyme. Thus, despite the marked difference in the relative amount of the 100,000- and 35,000-dalton ADA isozymes in man as compared to aves, the 100,000-dalton ADA isozymes from both species exhibit several similar kinetic properties, all of which are different from those of the 35,000-dalton ADA isozymes. We also report using a new sensitive assay, relative rates of degradation by the two chicken isozymes of several naturally occurring modified adenine nucleosides which are inhibitory to in vitro human lymphocyte proliferation.

摘要

在鸡肝脏中发现了两种动力学特性不同、分子量各异(35,000道尔顿和100,000道尔顿)的腺苷脱氨酶(ADA)同工酶,其含量大致相等。与35,000道尔顿的ADA相比,100,000道尔顿的ADA对腺苷的Km值显著更高,对脱氧腺苷的脱氨活性相对于腺苷则显著更低。直到最近才在哺乳动物组织中检测到100,000道尔顿的ADA同工酶,与鸡不同的是,它在总ADA活性中仅占微量成分。据报道,与人类35,000道尔顿的ADA同工酶相比,人类100,000道尔顿的ADA同工酶具有更高的Km值、更低的最适pH值以及对erythro-9-(2-羟基-2-壬基)腺嘌呤(EHNA)抑制作用的更强抗性。人类和鸟类100,000道尔顿的ADA同工酶在Km值上的相似性使我们推测,这些同工酶可能源自共同的祖先,因此在其他动力学参数方面也可能相似。我们现在报告,鸡的100,000道尔顿ADA与人类100,000道尔顿的同工酶一样,与鸟类或人类35,000道尔顿的同工酶相比,具有更低的最适pH值以及对EHNA抑制作用的更强抗性。此外,鸟类100,000道尔顿的同工酶对脱氧助间型霉素相对抗性较强,在pH 6.5时具有阴极而非阳极电泳迁移率。相反,我们报告人类100,000道尔顿的ADA同工酶与鸟类100,000道尔顿的ADA相似,对脱氧腺苷的相对脱氨活性明显低于35,000道尔顿的人类ADA同工酶。因此,尽管与鸟类相比,人类100,000道尔顿和35,000道尔顿的ADA同工酶的相对含量存在显著差异,但来自这两个物种的100,000道尔顿的ADA同工酶表现出几种相似的动力学特性,所有这些特性都与35,000道尔顿的ADA同工酶不同。我们还报告了使用一种新的灵敏测定法,测定两种鸡同工酶对几种天然存在的修饰腺嘌呤核苷的降解相对速率,这些核苷可抑制体外人类淋巴细胞增殖。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验