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5'-三磷酸阿糖腺苷对通透化小鼠P815肥大细胞中DNA合成的抑制作用。

Inhibition of DNA synthesis in permeabilized mouse P815 mast cells by arabinofuranosyladenine 5'-triphosphate.

作者信息

Geurtsen W, Zahn R K, Maidhof A, Schmidseder R, Müller W E

出版信息

Chemotherapy. 1981;27(1):61-7. doi: 10.1159/000237956.

Abstract

P815 mast cells (mouse leukemic cells) have been successfully permeabilized to 9-beta-arabinofuranosyladenine 5'-triphosphate (araATP) using lysolecithin. The permeabilized cells remained viable according to the following criteria: (a) exclusion of trypan blue after replacing the lysolecithin with culture medium; (b) cell growth rate identical to control cultures, and (c) intact DNA-synthesizing complex in permeable cells. It was shown that permeabilized cells incorporate [3H]thymidine and [3H]deoxyadenosine-triphosphate (dATP) into DNA when the suspension is supplied with the appropriate substrates and cofactors. Permeable cells break down araATP to 9-beta-D-arabinofuranosyladenine 5'-diphosphate only slightly after incubation for 60 min; no further dephosphorylation to 9-beta-D-arabinofuranosyladenine 5'-monophosphate or 9-beta-D-arabinofuranosyladenine occurs. In kinetic experiments it was shown that the DNA-replicating complex of permeabilized cells is competitively inhibited by araATP with respect to dATP; Ki(araATP) was determined to be 0.6 microM and the Km(dATP), 0.9 microM.

摘要

已使用溶血卵磷脂成功使P815肥大细胞(小鼠白血病细胞)对9-β-阿拉伯呋喃糖基腺嘌呤5'-三磷酸(araATP)通透。根据以下标准,通透后的细胞仍保持活力:(a)用培养基替换溶血卵磷脂后台盼蓝拒染;(b)细胞生长速率与对照培养物相同;(c)通透细胞中的DNA合成复合物完整。结果表明,当向悬浮液中提供适当的底物和辅因子时,通透细胞会将[3H]胸腺嘧啶核苷和[3H]脱氧腺苷三磷酸(dATP)掺入DNA。通透细胞在孵育60分钟后仅将araATP少量分解为9-β-D-阿拉伯呋喃糖基腺嘌呤5'-二磷酸;没有进一步去磷酸化为9-β-D-阿拉伯呋喃糖基腺嘌呤5'-单磷酸或9-β-D-阿拉伯呋喃糖基腺嘌呤。在动力学实验中表明,通透细胞的DNA复制复合物在dATP方面受到araATP的竞争性抑制;Ki(araATP)测定为0.6微摩尔,Km(dATP)为0.9微摩尔。

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