Loesser K E, Franzini-Armstrong C
University of Pennsylvania, School of Arts and Sciences, Department of Biology, Leidy Laboratory of Biology, Philadelphia, Pennsylvania 19104-6018.
J Struct Biol. 1990 Mar;103(1):48-56. doi: 10.1016/1047-8477(90)90085-q.
We present a simple approach for effective freeze-drying and rotary shadowing of large molecules, molecular assemblies, and cell organelles. Simply, a suspension of specimen is adsorped to a glass coverslip, stabilized, and rinsed with 30% methanol. A second coverslip is "sandwiched" on top, and excess methanol is withdrawn from the edges then frozen by plunging into liquid nitrogen and split. Following either rotary or unidirectional shadowing and replication, the coverslip is dissolved in hydrofluoric acid. In addition to avoiding the problems encountered with air-drying specimens for rotary shadowing, the technique also reproducibly provides the thin layer of solution necessary for proper freeze-drying, regardless of how hydrophobic the sample is. The "glass sandwich" technique allows modification of the glass substrate (making it hydrophobic with carbon or hydrophilic by soaking it in alcian blue) which clearly alters the shape of macromolecular assemblies such as myosin filaments and decorated thin filaments.
我们提出了一种用于大分子、分子聚集体和细胞器的有效冷冻干燥及旋转投影的简单方法。简单来说,将标本悬浮液吸附到玻璃盖玻片上,使其稳定,并用30%的甲醇冲洗。另一个盖玻片“夹”在上面,从边缘吸出多余的甲醇,然后通过浸入液氮中冷冻并劈开。在进行旋转或单向投影及复制之后,将盖玻片溶解于氢氟酸中。除了避免在旋转投影时空气干燥标本所遇到的问题外,该技术还能可重复地提供适当冷冻干燥所需的薄层溶液,而不管样品的疏水性如何。“玻璃夹层”技术允许对玻璃基板进行改性(用碳使其疏水或通过将其浸泡在阿尔辛蓝中使其亲水),这明显改变了诸如肌球蛋白丝和装饰细丝等大分子聚集体的形状。