将8-甲基腺苷引入2',5'-寡聚腺苷酸(2- 5a) 2'端可引起RNase L结合位点的剧烈移位。

Kumi Nagaoka, Seiya Kito, Yoshiaki Kitamura, Yoshihito Ueno, Yukio Kitade
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引用次数: 1

摘要

2',5'-寡聚腺苷酸(2- 5a)系统是干扰素(IFN)调控的RNA衰变途径,提供抗病毒感染的先天免疫。2-5A系统的生物学作用是由核糖核酸内切酶RNase L介导的,RNase L与2-5A结合后具有酶活性。据报道,2-5A的5'-磷酸化基团是RNase L激活所必需的。然而,我们发现在2'端具有8-甲基腺苷的5'- o -去磷酸化2- 5a四聚体类似物作为RNase L的激活剂比亲本2- 5a (p5'A2'p5'A2'p5'A2'p5'A2' p5' a2 ')更有效。8-甲基腺苷的引入被认为会引起RNase L结合位点的剧烈变化。
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Introduction of 8-methyladenosine into 2', 5'-oligoadenylate (2-5A) 2'-terminus induces dramatic shift in binding site of RNase L.

The 2',5'-oligoadenylate (2-5A) system is an interferon (IFN)-regulated RNA decay pathway that provides innate immunity against viral infections. The biological action of the 2-5A system is mediated by RNase L, an endoribonuclease that becomes enzymatically active after binding to 2-5A. It has been reported that the 5'-phosphoryl group of 2-5A is required for RNase L activation. However, we have found that 5'-O-dephosphorylated 2-5A tetramer analogs with 8-methyladenosine at the 2'-terminus were more effective as an activator of RNase L than the parent 2-5A (p5'A2'p5'A2'p5'A2'p5'A2'). Introduction of 8-methyladenosine is thought to induce a dramatic shift in the binding site of RNase L.

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