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公羊前顶体蛋白酶。一种分离无抑制剂的前顶体蛋白酶的简单方法及前顶体蛋白酶自激活研究。

Ram proacrosin. A simple method for isolation of proacrosin free of inhibitors, and proacrosin autoactivation studies.

作者信息

Cechová D, Jonáková V, Zelezná B, Petelíková J

出版信息

Andrologia. 1984 Sep-Oct;16(5):477-81. doi: 10.1111/j.1439-0272.1984.tb00400.x.

Abstract

Two partially purified proacrosin forms have been obtained from acid extracts of ram ejaculated spermatozoa by Sephadex G-100 column chromatography in 0.001 M HCl. The form obtained from the extracts of whole ejaculates with apparently higher molecular mass was free of any acrosin inhibitor and was used for autoactivation studies. The autoactivation followed a classical S-shaped activation curve and was a two-step process. The presence of calcium ions slowed down the autoactivation process and stabilized the active acrosin formed. The activity of latter rapidly decreased when the pH of the fully activated mixture was adjusted to pH 3. The activity was not restored by re-adjusting the pH to 8. A proacrosin with apparently lower molecular mass was isolated from the extract of washed spermatozoa. Both proacrosins, however, showed the same molecular mass Mr approximately 58 000 daltons, when examined by gel filtration in 0.1 M NaCl (pH 3).

摘要

通过在0.001 M盐酸中用葡聚糖G - 100柱色谱法,从公羊射出精子的酸性提取物中获得了两种部分纯化的前顶体蛋白酶形式。从整个射精提取物中获得的分子量明显较高的形式不含任何顶体蛋白酶抑制剂,并用于自激活研究。自激活遵循经典的S形激活曲线,是一个两步过程。钙离子的存在减缓了自激活过程,并稳定了形成的活性顶体蛋白酶。当将完全激活的混合物的pH值调节至pH 3时,后者的活性迅速下降。通过将pH值重新调节至8,活性无法恢复。从洗涤过的精子提取物中分离出一种分子量明显较低的前顶体蛋白酶。然而,当在0.1 M氯化钠(pH 3)中通过凝胶过滤检查时,两种前顶体蛋白酶都显示出相同的分子量Mr约为58000道尔顿。

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