首页> 美国卫生研究院文献>Biochemical Journal >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.
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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.

机译:组织培养细胞分级分离。由碳酸氢盐诱导的裂解作用使均化的125 I /内酯过氧化物酶标记的Lettrée细胞的细胞膜分级分离:通过区域离心以及蔗糖和甲氨amide呤梯度分离膜。

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摘要

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.
机译:1.Lettrée细胞在MF-1小鼠中腹膜内生长,并通过125I /乳过氧化物酶技术进行外在标记。 2.细胞在1 mM-NaHCO3中溶胀,并在Dounce匀浆器中破碎。 3.通过在BXIV带状转子中的沉降速率梯度离心,从后核上清液中分离出内质网,质膜和线粒体的粗级分。 4.这些膜的进一步分离是在等渗蔗糖梯度中进行的。 5.将来自后者的材料带以甲硝酰胺的梯度细分。获得了质膜和内质网的一些非常纯的亚组分。此外,解决了一个包含125I和NADPH-细胞色素c还原酶但不包含Na ++ K +刺激的腺苷三磷酸酶的亚组分,另一个包含这两种酶但不包含125I的亚组分。

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