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腺病毒感染会提高细胞拓扑异构酶I的水平。

Adenovirus infection elevates levels of cellular topoisomerase I.

作者信息

Chow K C, Pearson G D

出版信息

Proc Natl Acad Sci U S A. 1985 Apr;82(8):2247-51. doi: 10.1073/pnas.82.8.2247.

Abstract

We have developed a specific, sensitive, and quantitative assay for topoisomerase I, which is based on the formation of a covalent enzyme-DNA intermediate. Our assay measures the quantitative transfer of 32P radioactivity from 32P-labeled DNA to topoisomerase I. Since 32P-labeled topoisomerase molecules are resolved by NaDodSO4/PAGE, HeLa topoisomerase I (100 kDa) and calf thymus topoisomerase I (82 kDa) can be quantitatively assayed in the same reaction mixture. The assay can detect at least 0.3 ng (3 fmol) of topoisomerase I. We have used our assay to measure the levels of topoisomerase I activity in crude extracts of nuclei prepared from uninfected, adenovirus-infected, and adenovirus-transformed human cells. The evidence suggests that an adenovirus early gene product, presumably a protein encoded in early region 1A (E1A), increases cellular topoisomerase I activity at least 10-fold. Immunoblotting analysis with antiserum against calf thymus topoisomerase I shows that the increase in activity is due to an increase in the amount of enzyme.

摘要

我们基于共价酶 - DNA中间体的形成,开发了一种针对拓扑异构酶I的特异性、灵敏且定量的检测方法。我们的检测方法测量了32P放射性从32P标记的DNA到拓扑异构酶I的定量转移。由于32P标记的拓扑异构酶分子通过NaDodSO4/PAGE进行分离,因此可以在同一反应混合物中对HeLa拓扑异构酶I(100 kDa)和小牛胸腺拓扑异构酶I(82 kDa)进行定量检测。该检测方法至少能检测到0.3 ng(3 fmol)的拓扑异构酶I。我们已使用该检测方法来测量从未感染、腺病毒感染和腺病毒转化的人类细胞制备的细胞核粗提物中拓扑异构酶I的活性水平。证据表明,一种腺病毒早期基因产物,可能是早期区域1A(E1A)编码的一种蛋白质,可使细胞拓扑异构酶I的活性至少增加10倍。用抗小牛胸腺拓扑异构酶I的抗血清进行免疫印迹分析表明,活性的增加是由于酶量的增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2edf/397534/1c760192449d/pnas00348-0059-a.jpg

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