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博来霉素水解酶在两种中国仓鼠细胞系中的细胞内降解及其与培普利霉素敏感性的关系。

Intracellular degradation of bleomycin hydrolase in two Chinese hamster cell lines in relation to their peplomycin susceptibility.

作者信息

Nishimura C, Suzuki H, Tanaka N, Yamaguchi H

机构信息

Institute of Applied Microbiology, University of Tokyo, Japan.

出版信息

Biochim Biophys Acta. 1989 Jun 15;1012(1):29-35. doi: 10.1016/0167-4889(89)90007-4.

Abstract

The Chinese hamster lung (V79) cell was intrinsically 10-times more resistant to peplomycin, a bleomycin-related antitumor antibiotic, than the Chinese hamster ovary (CHO) cell. This may be associated with the 3-times higher levels of recovery of bleomycin hydrolase activity of the V79 cell. The degradation of bleomycin hydrolase molecules in both V79 and CHO cells was examined using a monoclonal antibody specific for the enzyme. Labelling experiments showed that the bleomycin hydrolase in CHO cells was less stable than the comparable enzyme in V79 cells, and that 48 kDa subunits comprising bleomycin hydrolase (a homohexameric enzyme) molecules were degraded into 31 kDa forms in both cell lines. The 105,000 X g pellet (microsomes) fraction obtained after subcellular fractionation of CHO cells contained both 48 kDa subunit and 31 kDa forms of bleomycin hydrolase, while the 105,000 X g supernatant cytosol fraction yielded only 48 kDa subunit forms of the enzyme. Moreover, bleomycin hydrolase activity of both V79 and CHO cells was almost entirely recovered from the cytosol fraction. These results suggest that degradation of the 48 kDa subunit form of bleomycin hydrolase in these two lines of cultured cells into the 31 kDa form occurs on the plasma membrane or the endoplasmic reticulum, with which the resulting large number of bleomycin hydrolase molecules or degraded forms of the enzyme that have lost enzymatic activity are associated.

摘要

中国仓鼠肺(V79)细胞对博来霉素相关的抗肿瘤抗生素培普利霉素的内在抗性比中国仓鼠卵巢(CHO)细胞高10倍。这可能与V79细胞中博来霉素水解酶活性的恢复水平高3倍有关。使用对该酶具有特异性的单克隆抗体检测了V79和CHO细胞中博来霉素水解酶分子的降解情况。标记实验表明,CHO细胞中的博来霉素水解酶比V79细胞中的同类酶更不稳定,并且在这两种细胞系中,构成博来霉素水解酶(一种同六聚体酶)分子的48 kDa亚基都降解为31 kDa形式。CHO细胞亚细胞分级分离后获得的105,000×g沉淀(微粒体)部分同时含有48 kDa亚基和31 kDa形式的博来霉素水解酶,而105,000×g上清液胞质溶胶部分仅产生48 kDa亚基形式的该酶。此外,V79和CHO细胞的博来霉素水解酶活性几乎完全从胞质溶胶部分中恢复。这些结果表明,在这两种培养细胞系中,博来霉素水解酶的48 kDa亚基形式降解为31 kDa形式发生在质膜或内质网上,由此产生大量与博来霉素水解酶分子或已失去酶活性的酶降解形式相关的物质。

相似文献

2
Mechanisms affecting peplomycin sensitivity of Chinese hamster cell lines.
J Antibiot (Tokyo). 1985 Sep;38(9):1257-65. doi: 10.7164/antibiotics.38.1257.

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