Pitha J, Pitha P M
Science. 1971 Jun 11;172(3988):1146-8. doi: 10.1126/science.172.3988.1146.
The antiviral activities of analogs of the double-stranded complex of polyinosinic and polycytidylic acids [poly(I).poly(C)], which is a potent interferon inducer, have been studied. Structural changes that modify the polymer backbone substantially, such as loops or 2' --> 5' phosphodiester bonds, lead to decreased antiviral activity. Unexpectedly, however, the complex of polyinosinic acid and poly(1-vinylcytosine), which is only a much more distantly related analog of poly(I) . poly(C), shows high activity. It is postulated that the high activity is related to the reduction of the charge/mass ratio and to the existence of this complex in an aggregated state; these are two factors that generally enhance the uptake of compo unds by cells.
聚肌苷酸和聚胞苷酸双链复合物[聚(I)·聚(C)]是一种有效的干扰素诱导剂,对其类似物的抗病毒活性进行了研究。对聚合物主链进行实质性修饰的结构变化,如环或2'→5'磷酸二酯键,会导致抗病毒活性降低。然而,出乎意料的是,聚肌苷酸和聚(1-乙烯基胞嘧啶)的复合物,它只是与聚(I)·聚(C)关系更为疏远的类似物,却表现出高活性。据推测,高活性与电荷/质量比的降低以及该复合物以聚集状态的存在有关;这是两个通常会增强细胞对化合物摄取的因素。