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DNA介导的人黑素瘤细胞表面糖蛋白gp130的转移:通过红细胞花环法鉴定转染子。

DNA-mediated transfer of human melanoma cell surface glycoprotein gp130: identification of transfectants by erythrocyte rosetting.

作者信息

Albino A P, Graf L H, Kantor R R, McLean W, Silagi S, Old L J

出版信息

Mol Cell Biol. 1985 Apr;5(4):692-7. doi: 10.1128/mcb.5.4.692-697.1985.

Abstract

DNA sequences encoding a human melanoma membrane-bound sialoglycoprotein of 130,000 molecular weight (gp130) were introduced into a clonal derivative of mouse B-16 melanoma cells with the selectable neomycin resistance gene (aminoglycoside phosphotransferase). Mouse transfectants were identified by a rapid and precise screening method with mouse monoclonal antibodies and erythrocyte rosetting. The frequency of gp130 transfectants was approximately 1 in 2,000 to 5,000 colonies with neo+ cells. Analysis of secondary mouse transfectants has revealed that the transfected gp130 has a molecular weight, isoelectric point, intracellular processing, peptide map, and spatial orientation of surface-exposed epitopes indistinguishable from those seen with gp130 from human melanoma cells. In contrast to primary transfectants, secondary transfectants expressing gp130 lack demonstrable human repetitive sequences.

摘要

将编码分子量为130,000的人黑色素瘤膜结合唾液糖蛋白(gp130)的DNA序列与可选择的新霉素抗性基因(氨基糖苷磷酸转移酶)一起导入小鼠B - 16黑色素瘤细胞的克隆衍生物中。通过使用小鼠单克隆抗体和红细胞花环形成的快速精确筛选方法鉴定小鼠转染子。gp130转染子的频率约为每2000至5000个带有neo +细胞的菌落中有1个。对第二代小鼠转染子的分析表明,转染的gp130的分子量、等电点、细胞内加工、肽图谱以及表面暴露表位的空间取向与人黑色素瘤细胞的gp130所见的那些无法区分。与原代转染子相反,表达gp130的第二代转染子缺乏可证明的人重复序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c00/366771/9ebbc8abf3d9/molcellb00100-0107-a.jpg

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