Schröder H C, Kelve M, Müller W E
Abteilung Angewandte Molekularbiologie, Johannes Gutenberg-Universität, Mainz, Germany.
Prog Mol Subcell Biol. 1994;14:176-97. doi: 10.1007/978-3-642-78549-8_10.
2',5'-Oligoadenylates (2-5A) have an essential role in the establishment of the antiviral state of a cell exposed to virus infection. The key enzymes of the 2-5A system are the 2-5A forming 2',5'-oligoadenylate synthetase (2-5OAS), the activity of which depends on the presence of viral or cellular double-stranded RNA (dsRNA), and the 2-5A-activated ribonuclease (RNase L). Basic research in recent years has shown that the 2-5A system is a promising target for anti-HIV chemotherapy, particularly due to its interaction with double-stranded segments within HIV RNA. Two new strategies have been developed which yield a selective antiviral effect of 2-5A against HIV-1 infection: (1) development of 2-5A analogues displaying a dual mode of action (activation of RNase L and inhibition of HIV-1 RT) and (2) intracellular immunization of cells against HIV-1 infection by application of the HIV-1-LTR--2-5OAS hybrid gene. A further strategy is the inhibition of DNA topoisomerase I by longer 2-5A oligomers.
2',5'-寡腺苷酸(2-5A)在细胞建立针对病毒感染的抗病毒状态过程中发挥着重要作用。2-5A系统的关键酶是形成2-5A的2',5'-寡腺苷酸合成酶(2-5OAS),其活性取决于病毒或细胞双链RNA(dsRNA)的存在,以及2-5A激活的核糖核酸酶(RNase L)。近年来的基础研究表明,2-5A系统是抗HIV化疗的一个有前景的靶点,特别是因为它与HIV RNA中的双链片段相互作用。已经开发出两种新策略,可使2-5A对HIV-1感染产生选择性抗病毒作用:(1)开发具有双重作用模式(激活RNase L和抑制HIV-1逆转录酶)的2-5A类似物,以及(2)通过应用HIV-1-LTR-2-5OAS杂交基因对细胞进行针对HIV-1感染的细胞内免疫。另一种策略是用更长的2-5A寡聚物抑制DNA拓扑异构酶I。