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嗜热四膜虫分离纤毛微管上ATP酶的亚细胞定位

Em localization of atpase on microtubules of isolated cilia from Tetrahymena vorax.

作者信息

Fitzsimons J T, Kerkut G A

出版信息

Comp Biochem Physiol A Comp Physiol. 1983;74(3):739-43. doi: 10.1016/0300-9629(83)90577-7.

Abstract
  1. Isolated cilia were prepared from Tetrahymena vorax using the local anaesthetic dibucaine in the deciliation step. 2. ATPase was cytochemically localized on microtubules of isolated cilia using the Washstein-Meisel incubation; deposition of lead phosphate indicated the sites of enzyme activity. 3. Mild fixation conditions gave optimum localizations. Satisfactory results were attained using 0.5% glutaraldehyde with a fixation time of 30 min. 4. An increase in ATPase activity, as judged by lead phosphate precipitation, was observed when cytochemical incubations were increased from 5 min to 1 hr. An incubation time of 15 min gave optimum results. 5. No advantage was gained with incubation times over 1 hr as diffusion of reaction product may occur. 6. No ATPase activity was observed in control incubations where the enzyme substrate ATP was omitted. 7. Purified cilia preparations provide useful starting material for the study of microtubular ATPase.
摘要
  1. 在去纤毛步骤中,使用局部麻醉剂丁卡因从嗜热四膜虫制备分离的纤毛。2. 使用沃什斯坦 - 迈泽尔孵育法,通过细胞化学方法将ATP酶定位在分离纤毛的微管上;磷酸铅的沉积表明了酶活性位点。3. 温和的固定条件可实现最佳定位。使用0.5%戊二醛固定30分钟可获得满意结果。4. 当细胞化学孵育时间从5分钟增加到1小时时,通过磷酸铅沉淀判断,ATP酶活性增加。孵育15分钟可获得最佳结果。5. 孵育时间超过1小时没有优势,因为可能会发生反应产物扩散。6. 在省略酶底物ATP 的对照孵育中未观察到ATP酶活性。7. 纯化的纤毛制剂为微管ATP酶的研究提供了有用的起始材料。

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