Smith G P, MacGregor R R, Peters T J
Biochim Biophys Acta. 1982 Dec 17;719(3):532-8. doi: 10.1016/0304-4165(82)90243-4.
Polymorphonuclear leukocytes were isolated from the peripheral blood of rabbits by Ficoll-Hypaque centrifugation followed by dextran sedimentation. The granulocytes were homogenized in isotonic sucrose and subjected to analytical subcellular fractionation by sucrose density gradient centrifugation. Leucine aminopeptidase, when assayed with L-leucine-7-amido-4-methyl-coumarin as substrate, showed a similar distribution to N-acetyl-beta-glucosaminidase and thus is localized to the tertiary granules. There was no leucine aminopeptidase associated with the plasma membrane of these cells. Further experiments with purified plasma membranes and inhibitor studies using diazotized sulphanilic acid further confirmed that leucine aminopeptidase had a purely intracellular localization. Vitamin B-12 binding protein showed a similar localization to alkaline phosphatase indicating that, as in human polymorphonuclear leukocytes, vitamin B-12 binding protein is located to the specific granules.
通过Ficoll-Hypaque离心法继以葡聚糖沉降从兔外周血中分离出多形核白细胞。将粒细胞在等渗蔗糖中匀浆,并通过蔗糖密度梯度离心进行分析性亚细胞分级分离。以L-亮氨酸-7-氨基-4-甲基香豆素为底物进行测定时,亮氨酸氨肽酶显示出与N-乙酰-β-葡萄糖苷酶相似的分布,因此定位于三级颗粒。这些细胞的质膜未发现有亮氨酸氨肽酶。使用纯化的质膜进行的进一步实验以及利用重氮化磺胺酸的抑制剂研究进一步证实亮氨酸氨肽酶完全定位于细胞内。维生素B12结合蛋白显示出与碱性磷酸酶相似的定位,表明与人类多形核白细胞一样,维生素B12结合蛋白定位于特异性颗粒。