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静止和分裂的艾氏腹水瘤细胞中非组蛋白染色体蛋白的标记模式。

Labelling pattern of the nonhistone chromosomal proteins in quiescent and dividing Ehrlich ascites tumour cells.

作者信息

Anachkova B, Russev G

出版信息

Int J Biochem. 1983;15(8):1093-4. doi: 10.1016/0020-711x(83)90050-2.

Abstract

Upon pulse-labelling with [14C]protein hydrolizate both in dividing and quiescent Ehrlich ascites tumour (EAT) cells the nonhistone chromosomal (NHC) proteins had uniform specific radioactivity with few exceptions: Both in quiescent and dividing EAT cells a polypeptide with molecular weight of about 200 kdalton had specific radioactivity 2-3 times lower than that of the most of the NHC proteins. In the actively proliferating cells a group of proteins with molecular weights between 45 and 65 kdalton had 2-3 times higher specific radioactivity than most of the NHC proteins. In quiescent cells the specific radioactivity of a group of proteins with molecular weights in the range 18-25 kdalton was 3-4 times higher than that of the rest of the NHC proteins.

摘要

在用[14C]蛋白水解物对分裂期和静止期的艾氏腹水瘤(EAT)细胞进行脉冲标记后,非组蛋白染色体(NHC)蛋白具有均匀的比放射性,只有少数例外:在静止期和分裂期的EAT细胞中,一种分子量约为200千道尔顿的多肽的比放射性比大多数NHC蛋白低2至3倍。在活跃增殖的细胞中,一组分子量在45至65千道尔顿之间的蛋白的比放射性比大多数NHC蛋白高2至3倍。在静止期细胞中,一组分子量在18至25千道尔顿范围内的蛋白的比放射性比其余NHC蛋白高3至4倍。

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