Max E E, Goodman D B, Rasmussen H
Biochim Biophys Acta. 1978 Aug 4;511(2):224-39. doi: 10.1016/0005-2736(78)90316-4.
A new technique has been developed for the isolation of membrane vesicles from the vitamin D-deficient and vitamin D-treated chick intestinal brush border membrane. The technique involves removal of nuclei from a low speed pellet by discontinuous sucrose gradient centrifugation. The resulting intact brush borders are then homogenized in 0.5 M Tris and the membrane fragments purified on a glycerol gradient. This preparation represents a 20-fold purification of the brush border marker sucrase. After 1alpha-hydroxyvitamin D3 treatment there is a significant increase in membrane phospholipid phosphorous, an alteration in the fatty acid composition of the phosphatidylcholine fraction of membrane phospholipid, and a decrease in sucrase specific activity.
已开发出一种新技术,用于从维生素D缺乏和经维生素D处理的雏鸡肠道刷状缘膜中分离膜泡。该技术包括通过不连续蔗糖梯度离心从低速沉淀中去除细胞核。然后将得到的完整刷状缘在0.5 M Tris中匀浆,并在甘油梯度上纯化膜片段。这种制备物代表刷状缘标记蔗糖酶的20倍纯化。经1α-羟基维生素D3处理后,膜磷脂磷显著增加,膜磷脂磷脂酰胆碱部分的脂肪酸组成发生改变,蔗糖酶比活性降低。