Kellenberger E, Dürrenberger M, Villiger W, Carlemalm E, Wurtz M
J Histochem Cytochem. 1987 Sep;35(9):959-69. doi: 10.1177/35.9.3302020.
The surface of thin sections of aldehyde-fixed biological material shows a specimen-related relief of 2-6 nm with Lowicryl. Epon sections are about three times smoother. The relief is the consequence of thin-sectioning being in reality a cleavage. Epitopes are supposed to be laid open (or set free) because cleavage follows the interfaces between protein and Lowicryl. We have developed a simple theory on this basis and have theoretically estimated the efficiency of on-section labeling and compared it with experimental data. For randomly dispersed proteins in cytoplasm, Lowicryl sections will yield significant label only when the concentration of the antigen is about 10 microM or more. The complex situation of more compact proteins, as represented by fibers, sheets, and biological membranes is discussed and the difficulty of significant calculations is explained. Pre-embedding labeling and melted cryosections should give 10-30 times more label. The possible reasons for the observed much smaller gain of not more than two to three times are discussed.
经醛固定的生物材料薄片表面,用Lowicryl包埋时会呈现出与标本相关的2 - 6纳米起伏。环氧树脂包埋的切片则要光滑约三倍。这种起伏是因为实际上薄切片是一种切割过程。表位被认为是由于切割沿着蛋白质与Lowicryl之间的界面进行而被暴露(或释放)出来。我们在此基础上建立了一个简单理论,并从理论上估计了切片上标记的效率,并将其与实验数据进行了比较。对于细胞质中随机分散的蛋白质,只有当抗原浓度约为10微摩尔或更高时,Lowicryl切片才会产生显著的标记。文中讨论了由纤维、薄片和生物膜所代表的更为紧密的蛋白质的复杂情况,并解释了进行显著计算的困难。预包埋标记和融化的冰冻切片应该能产生多10 - 30倍的标记。文中还讨论了观察到的不超过两到三倍的小得多的增益的可能原因。