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从10号线肝癌细胞和质膜中提取肿瘤特异性抗原。

Extraction of tumor-specific antigen from cells and plasma membranes of line-10 hepatoma.

作者信息

Leonard E J, Richardson A K, Hardy A S, Rapp H J

出版信息

J Natl Cancer Inst. 1975 Jul;55(1):73-9. doi: 10.1093/jnci/55.1.73.

Abstract

Tumor-specific antigen was extracted with 3 M KCl from line-10 guinea pig hepatoma cells. The yield of antigenic activity, estimated by production of delayed cutaneous hypersensitivity reactions in line-10 immune guinea pigs, was 10-30% of the antigen present in intact cells. By ultracentrifugation criteria, the extracted antigen was soluble. Gel filtration, ion exchange chromatography, and salting-out studies showed that the antigen was heterogeneous in size and net charge. The possibility that 3 M KCl extracted a homogeneous population of molecules associating into polymers of various sizes at low ionic strength was ruled out by heterogeneity on Sephadex G-200 chromatography at high ionic strength. After osmotic lysis of sucrose-loaded line-10 cells, whole plasma membranes or large membrane fragments were obtained in a yield of about 20%. The isolation procedure did not cause detectable loss of membrane antigenic activity. The membranes had 33 skin test U/mg membrane protein, compared to the intact cell value of 1.7 skin test U/mg cell protein. Extracts of plasma membranes had 10-20% of the antigenic activity of the starting membrane material. In contrast to the wide variety of proteins liberated from intact cells, much of the protein extracted from the membranes was in the molecular weight range above 250,000.

摘要

用3M氯化钾从10号线豚鼠肝癌细胞中提取肿瘤特异性抗原。通过在10号线免疫豚鼠中产生迟发型皮肤超敏反应来估计抗原活性产量,其为完整细胞中抗原的10%-30%。根据超速离心标准,提取的抗原是可溶的。凝胶过滤、离子交换色谱和盐析研究表明,该抗原在大小和净电荷方面是异质的。高离子强度下在葡聚糖凝胶G-200色谱上的异质性排除了3M氯化钾提取了在低离子强度下缔合成各种大小聚合物的同质分子群体的可能性。在对加载蔗糖的10号线细胞进行渗透裂解后,获得了全细胞膜或大的膜片段,产量约为20%。分离过程未导致膜抗原活性的可检测损失。这些膜具有33皮肤试验单位/毫克膜蛋白,而完整细胞的值为1.7皮肤试验单位/毫克细胞蛋白。质膜提取物具有起始膜材料抗原活性的10%-20%。与从完整细胞中释放的多种蛋白质相比,从膜中提取的大部分蛋白质的分子量范围在250,000以上。

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