Persechini P M, Liu C C, Detmers P A, Young J D
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY 10021.
J Immunol Methods. 1989 Nov 13;124(1):7-15. doi: 10.1016/0022-1759(89)90179-8.
A separation procedure based on Percoll gradient centrifugation is described here that allows enrichment for two main populations of granules, with average densities of 1.05 and 1.1 g/ml. The heavy-density granules, which comprise 5-20% of the total amount of membrane-lytic activity, are morphologically and biochemically more homogeneous than the light-density granules, which are contaminated with other subcellular organelles. A trypsin-like serine esterase activity, used in the past as a granule marker, was mainly found in the free cytosol and in the light-density fractions, while a small portion of this activity was associated with the heavy-density fractions. This enzyme marker is therefore not exclusively associated with granules and should not be used as the only granule marker.
本文描述了一种基于Percoll梯度离心的分离方法,该方法可富集两种主要的颗粒群体,其平均密度分别为1.05和1.1 g/ml。重密度颗粒占膜溶解活性总量的5%-20%,在形态和生化方面比被其他亚细胞器污染的轻密度颗粒更均匀。过去用作颗粒标记物的胰蛋白酶样丝氨酸酯酶活性主要存在于游离胞质溶胶和轻密度组分中,而该活性的一小部分与重密度组分相关。因此,这种酶标记物并非仅与颗粒相关,不应仅用作颗粒标记物。