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含硫代嘧啶的多聚核糖核苷酸对干扰素的诱导作用。

Induction of interferon by polyribonucleotides containing thiopyrimidines.

作者信息

Reuss K, Scheit K H, Saiko O

出版信息

Nucleic Acids Res. 1976 Oct;3(10):2861-75. doi: 10.1093/nar/3.10.2861.

Abstract

The influence of thioketo substitution in pyrimidine bases of double-stranded polynucleotides on interferon induction was investigated. The stabilizing effect of 2-thioketo substitution was reflected in the increased interferon inducing activity of poly(A-s2U) over that of poly(A-U). Poly(A-s2U) and poly(I)-poly(s2C) were as effective as poly(I)-Poly(C) in rabbit cells. Poly(I)-poly(C) and poly(I)-poly(s2C) were compared in several animal species. No differences in biological effects were observed in rabbits and dogs. In rodents, poly(I)-poly(s2C) was less effective and less toxic.Poly(I)-poly(s2C) was highly resistant against degradation by human serum. Further investigations seem to be justified to elucidate whether this property offers any advantages for the potential clinical utilization of poly(I)-poly(s2C).

摘要

研究了双链多核苷酸嘧啶碱基中的硫酮取代对干扰素诱导的影响。2-硫酮取代的稳定作用体现在聚(A-s2U)的干扰素诱导活性高于聚(A-U)。聚(A-s2U)和聚(I)-聚(s2C)在兔细胞中与聚(I)-聚(C)一样有效。在几种动物物种中比较了聚(I)-聚(C)和聚(I)-聚(s2C)。在兔和狗中未观察到生物学效应的差异。在啮齿动物中,聚(I)-聚(s2C)效果较差且毒性较小。聚(I)-聚(s2C)对人血清降解具有高度抗性。进一步的研究似乎有必要阐明该特性是否为聚(I)-聚(s2C)的潜在临床应用提供任何优势。

相似文献

2
Interferon inducing activity of polyinosinic acid.聚肌苷酸的干扰素诱导活性
J Gen Virol. 1978 Jul;40(1):203-12. doi: 10.1099/0022-1317-40-1-203.

本文引用的文献

7
A new polynucleotide complex poly(s 2 C)-poly(I).一种新的多核苷酸复合物聚(s2C)-聚(I)。
Eur J Biochem. 1972 May;27(1):109-15. doi: 10.1111/j.1432-1033.1972.tb01816.x.
8
Synthesis and properties of poly(s 2 C), a new poly(C) analog.新型聚(C)类似物聚(s2C)的合成与性质
Eur J Biochem. 1971 Dec;24(2):385-92. doi: 10.1111/j.1432-1033.1971.tb19697.x.
10

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