Hohenberg H, Mannweiler K, Müller M
Heinrich-Pette-Institute for Experimental Virology and Immunology, University of Hamburg, Germany.
J Microsc. 1994 Jul;175(Pt 1):34-43. doi: 10.1111/j.1365-2818.1994.tb04785.x.
A procedure for efficient cryoimmobilization of large volumes of cell suspensions or micro-organisms by high-pressure freezing is described. This procedure uses transparent, porous cellulose capillary tubes with an inner diameter of 200 microns, into which the suspensions are drawn by capillary action. The tubes are processed by high-pressure freezing and freeze-substitution as if they were tissue samples. Centrifugation of suspensions at low temperatures is no longer necessary and cryopreparation is greatly facilitated. A very high yield of adequately frozen specimens is obtained due to the constant, defined sample geometry. This approach can also be used to process suspensions by conventional chemical fixation, eliminating the need to embed pellets in low-melting-point agarose, for example, prior to chemical fixation. The preparation procedure is demonstrated with suspensions of nematodes, paramecia and bacteria.
描述了一种通过高压冷冻对大量细胞悬液或微生物进行高效冷冻固定的方法。该方法使用内径为200微米的透明多孔纤维素毛细管,通过毛细管作用将悬液吸入其中。这些管子像组织样本一样经过高压冷冻和冷冻置换处理。不再需要在低温下对悬液进行离心,极大地简化了冷冻制备过程。由于样本几何形状恒定且明确,可获得高产率的充分冷冻标本。这种方法也可用于通过传统化学固定处理悬液,例如无需在化学固定前将沉淀颗粒包埋在低熔点琼脂糖中。用线虫、草履虫和细菌的悬液展示了制备过程。