Vollenweider H J, Sogo J M, Koller T
Proc Natl Acad Sci U S A. 1975 Jan;72(1):83-7. doi: 10.1073/pnas.72.1.83.
A protein-free nucleic acid preparation method for electron microscopy is described. The basic procedure is very similar to the classical protein monolayer spreading techniques. The carrier protein (usually cytochrome c) is replaced by benzyldimethylalkylammonium chloride. Both the hypophase method and the microdiffusion or droplet method can be applied with this compound. Unlike cytochrome c, benzyldimethylalkylammonium chloride does not lead to any apparent thickening of the nucleic acid strands. Partially denatured DNA spread with this reagent shows a loosened structure with a foamy appearance in the regions previously considered to be "unmelted," which open up locally into melted loops of different size. Specifically bound proteins, such as RNA polymerase on bacteriophage T7 DNA, can be detected unambiguously.
描述了一种用于电子显微镜的无蛋白质核酸制备方法。基本程序与经典的蛋白质单层铺展技术非常相似。载体蛋白(通常是细胞色素c)被苄基二甲基烷基氯化铵取代。这种化合物可应用下相法和微扩散或液滴法。与细胞色素c不同,苄基二甲基烷基氯化铵不会导致核酸链有任何明显的增厚。用这种试剂铺展的部分变性DNA在以前被认为是“未熔解”的区域呈现出结构疏松且有泡沫外观,这些区域会局部打开形成不同大小的熔解环。可以明确检测到特异性结合的蛋白质,如噬菌体T7 DNA上的RNA聚合酶。