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通过冷冻干燥对线粒体偶联因子F1(ATP酶)进行可视化观察。

Visualization of mitochondrial coupling factor F1(ATPase) by freeze-drying.

作者信息

Sikerwar S S, Malhotra S K

出版信息

Cell Biophys. 1979 Mar;1(1):55-63. doi: 10.1007/BF02785056.

Abstract

It is known that the negatively stained preparations of inner mitochondrial membrane display characteristic approximately 9 nm F1 (ATPase) knobs projecting from the matrix surface. Freeze-etch studies have reported the absence of such knobs from the "etched" surface of the inner mitochondrial membranes. We have demonstrated their presence on the surface of SMP (submitochondrial particles) prepared by freeze-drying for transmission electron microscopy. This identification has been substantiated by comparison with freeze-dried TU particles (trypsin-urea treated SMP) that are devoid of F1 (ATPase). It has been suggested that a layer of water molecules is strongly adsorbed to the surface of SMP and does not sublime during normal freeze-"etching."

摘要

已知线粒体内膜的负染色制剂显示出从基质表面突出的特征性约9纳米F1(ATP酶)旋钮。冷冻蚀刻研究报告称,线粒体内膜的“蚀刻”表面没有这种旋钮。我们已经通过冷冻干燥制备用于透射电子显微镜观察的亚线粒体颗粒(SMP)表面证明了它们的存在。通过与不含F1(ATP酶)的冷冻干燥的TU颗粒(胰蛋白酶-尿素处理的SMP)进行比较,证实了这一鉴定结果。有人提出,一层水分子强烈吸附在SMP表面,在正常冷冻“蚀刻”过程中不会升华。

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