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2',5'-寡腺苷酸对病毒逆转录酶的抑制作用。

Inhibition of viral reverse transcriptase by 2',5'-oligoadenylates.

作者信息

Liu D K, Owens G F

出版信息

Biochem Biophys Res Commun. 1987 May 29;145(1):291-7. doi: 10.1016/0006-291x(87)91319-2.

Abstract

Viral reverse transcriptase activity was inhibited in a concentration dependent manner by 2',5'-oligoadenylate. Kinetically this inhibition was of a mixed type where 2',5'-oligoadenylate was not strictly competitive with dTTP. The potency of inhibition was more marked in the absence than in the presence of sulfhydryl agents. 2',5'-oligoadenylate had no effect on DNA-dependent E. coli DNA polymerase and was much less active against mammalian DNA polymerases. This is the first report of reverse transcriptase inhibition by an inducible constitutive natural ligand.

摘要

2',5'-寡腺苷酸以浓度依赖性方式抑制病毒逆转录酶活性。从动力学角度来看,这种抑制属于混合型,其中2',5'-寡腺苷酸与dTTP并非严格竞争关系。在不存在巯基试剂的情况下,抑制效力比存在时更为显著。2',5'-寡腺苷酸对依赖DNA的大肠杆菌DNA聚合酶没有影响,对哺乳动物DNA聚合酶的活性也低得多。这是关于诱导性组成型天然配体抑制逆转录酶的首次报道。

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