Liu D K, Owens G F
Biochem Biophys Res Commun. 1987 May 29;145(1):291-7. doi: 10.1016/0006-291x(87)91319-2.
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.
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。