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一种人类癌细胞的新标志物。1. Ca抗原和Ca1抗体。

A new marker for human cancer cells. 1 The Ca antigen and the Ca1 antibody.

作者信息

Ashall F, Bramwell M E, Harris H

出版信息

Lancet. 1982 Jul 3;2(8288):1-6. doi: 10.1016/s0140-6736(82)91150-3.

Abstract

In a search for antibodies that might distinguish between malignant and non-malignant cells a panel of matched pairs of hybrid cells produced by fusion of diploid fibroblasts with malignant cells originating from a cervical carcinoma was used as a screen. Each pair consisted of a hybrid in which malignancy was suppressed and a malignant segregant derived from this hybrid. A monoclonal antibody, designated Ca1, was found that discriminated absolutely between the hybrids in which malignancy was suppressed and the malignant segregants. This antibody detected an antigen present in the cell membranes of a wide variety of malignant human cells lines but not of diploid human cell strains. The antigen was found in very low concentrations, if at all, in homogenates of normal adult or fetal tissues. It could be immunoprecipitated by the Ca1 antibody from extracts of malignant cells but not from extracts of non-malignant cells. After reduction, the immunoprecipitated antigen separated in sodium dodecyl sulphate acrylamide gels as two bands with proximate molecular masses of 390 000 and 350 000. These two components had a properties of glycoproteins with a high carbohydrate content; both bound the Ca1 antibody. The antigenic determinant resisted boiling at 100 degrees C and extraction by range of organic solvents. The binding of the Ca1 antibody to the antigen was substantially reduced by treatment of the antigen with neuraminidase, and the antigenic determinant was largely destroyed by certain endoglycosidases and by extensive proteolysis. Pending its further characterisation, this antigen had been called the Ca antigen.

摘要

为了寻找能够区分恶性细胞和非恶性细胞的抗体,一组由二倍体成纤维细胞与源自宫颈癌的恶性细胞融合产生的配对杂交细胞被用作筛选对象。每一对包括一个恶性被抑制的杂交细胞和一个源自该杂交细胞的恶性分离体。发现了一种名为Ca1的单克隆抗体,它能绝对地区分恶性被抑制的杂交细胞和恶性分离体。这种抗体能检测到多种恶性人类细胞系细胞膜上存在的一种抗原,但在二倍体人类细胞株的细胞膜上则检测不到。在正常成人或胎儿组织的匀浆中,即使有这种抗原,其浓度也非常低。它能被Ca1抗体从恶性细胞提取物中免疫沉淀出来,但不能从非恶性细胞提取物中免疫沉淀出来。还原后,免疫沉淀的抗原在十二烷基硫酸钠聚丙烯酰胺凝胶中分离为两条带,其近似分子量分别为390 000和350 000。这两种成分具有高碳水化合物含量的糖蛋白特性;两者都能与Ca1抗体结合。抗原决定簇能抵抗100℃煮沸和多种有机溶剂的提取。用神经氨酸酶处理抗原后,Ca1抗体与抗原的结合显著减少,某些内切糖苷酶和广泛的蛋白水解作用能大大破坏抗原决定簇。在对其进行进一步鉴定之前,这种抗原被称为Ca抗原。

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