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组织培养细胞分级分离。通过碳酸氢盐诱导裂解对125I/乳过氧化物酶标记的Lettrée细胞匀浆后的细胞膜进行分级分离:通过区带离心以及在蔗糖和甲泛葡胺梯度中分离细胞膜。

Tissue-culture cell fractionation. Fractionation of cellular membranes from 125I/lactoperoxidase-labelled Lettrée cells homogenized by bicarbonate-induced lysis: resolution of membranes by zonal centrifugation and in sucrose and metrizamide gradients.

作者信息

Graham J M, Coffey K H

出版信息

Biochem J. 1979 Jul 15;182(1):173-80. doi: 10.1042/bj1820173.

Abstract
  1. Lettrée cells were grown intraperitoneally in MF-1 mice and labelled extrinsically by the 125I/lactoperoxidase technique. 2. The cells were swollen in 1 mM-NaHCO3 and disrupted in a Dounce homogenizer. 3. Crude fractions of endoplasmic reticulum, plasma membrane and mitochondria were separated from a post-nuclear supernatant by sedimentation-rate gradient centrifugation in a BXIV zonal rotor. 4. Further resolution of these membranes was carried out in isopycnic sucrose gradients. 5. Bands of material from the latter were subfractionated in gradients of metrizamide. Some very pure subfractions of plasma membrane and endoplasmic reticulum were obtained. In addition, one subfraction containing 125I and NADPH-cytochrome c reductase but no Na++K+-stimulated adenosine triphosphatase and another containing these two enzymes but no 125I were resolved.
摘要
  1. 将已分化细胞接种于MF-1小鼠腹腔内生长,并用¹²⁵I/乳过氧化物酶技术进行体外标记。2. 细胞在1 mM碳酸氢钠中肿胀,然后在玻璃匀浆器中破碎。3. 通过在BXIV区带转子中进行沉降速率梯度离心,从核后上清液中分离出内质网、质膜和线粒体的粗提组分。4. 这些膜在等密度蔗糖梯度中进一步分离。5. 后者的物质条带在甲泛葡胺梯度中进行亚分级分离。获得了一些非常纯的质膜和内质网亚组分。此外,还分离出了一个含有¹²⁵I和NADPH-细胞色素c还原酶但没有钠钾刺激的三磷酸腺苷酶的亚组分,以及另一个含有这两种酶但没有¹²⁵I的亚组分。

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1
Isolation of plasma membrane glycoprotein from bovine thymocytes.
Biochim Biophys Acta. 1977 Mar 1;465(2):341-52. doi: 10.1016/0005-2736(77)90083-9.
3
Exposed protein on the intact human erythrocyte.完整人类红细胞上暴露的蛋白质。
Biochemistry. 1971 May 11;10(10):1766-71. doi: 10.1021/bi00786a006.
4
The enzymatic iodination of the red cell membrane.红细胞膜的酶促碘化作用。
J Cell Biol. 1972 Nov;55(2):390-405. doi: 10.1083/jcb.55.2.390.

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