Pies N J, Wohlfarth-Bottermann K E
Eur J Cell Biol. 1986 Apr;40(2):139-49.
Cell-free models should offer "in situ conditions" to study the physiology of cytoplasmic actomyosin in its natural environment, while, if possible, still associated with its regulatory control proteins and other cytoplasmic components. Detergents and glycerol as the usual media to permeabilize the plasmalemma and to extract a portion of the cytoplasmic components, are accompanied by several disadvantages. We investigated a cell-free model consisting of cryosections of plasmodial strands that were previously enriched with "stress fibrils" and fluorescently labelled with phallotoxins and that contain the non-denatured structures that are to be reactivated in situ. The contraction reaction can be directly observed in the fluorescence microscope. This procedure allows the study of contraction conditions in the natural environment of the fibrils. The aim of these reactivation experiments was to identify the role of calcium ions. According to our results, a reactivation of cryosections is not Ca++ dependent but is partly inhibited at concentrations of 10(-4) to 5 X 10(-2)M Ca++. Complete inhibition occurs at 10 to 20 mM Ca++. Electron microscopical investigations revealed that the fluorescently labelled contracting structures were identical to actomyosin fibrils.
无细胞模型应提供“原位条件”,以在其天然环境中研究细胞质肌动球蛋白的生理学,同时,如果可能的话,仍与其调节控制蛋白和其他细胞质成分相关联。作为使质膜通透并提取一部分细胞质成分的常用介质,去污剂和甘油存在几个缺点。我们研究了一种无细胞模型,该模型由疟原质体链的冷冻切片组成,这些冷冻切片先前富含“应力纤维”,并用鬼笔环肽进行了荧光标记,并且包含将在原位重新激活的非变性结构。收缩反应可以在荧光显微镜下直接观察到。该程序允许在纤维的天然环境中研究收缩条件。这些重新激活实验的目的是确定钙离子的作用。根据我们的结果,冷冻切片的重新激活不依赖于Ca++,但在10(-4)至5×10(-2)M Ca++的浓度下会受到部分抑制。在10至20 mM Ca++时会完全抑制。电子显微镜研究表明,荧光标记的收缩结构与肌动球蛋白纤维相同。