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1
Antiviral activity of polynucleotides: copolymers of inosinic acid and N2-dimethylguanylic of 2-methylthioinosinic acid.多核苷酸的抗病毒活性:肌苷酸与2-甲硫基肌苷酸的N2-二甲基鸟苷酸共聚物。
Nucleic Acids Res. 1975 Jan;2(1):121-9. doi: 10.1093/nar/2.1.121.
2
Antiviral activity of polynucleotides: poly(2'-fluoro-2'-deoxyuridylic acid).多核苷酸的抗病毒活性:聚(2'-氟-2'-脱氧尿苷酸)。
Biochim Biophys Acta. 1973 Sep 28;324(1):50-6. doi: 10.1016/0005-2787(73)90249-9.
3
A potent interferon inducer derived from poly (7-deazainosinic acid).一种源自聚(7-脱氮肌苷酸)的强效干扰素诱导剂。
Biochemistry. 1974 Oct 8;13(21):4400-8. doi: 10.1021/bi00718a025.
4
Interferon induction by synthetic polynucleotides: importance of purine N-7 and strandwise rearrangement.合成多核苷酸诱导干扰素:嘌呤N-7和链间重排的重要性
Proc Natl Acad Sci U S A. 1974 Jan;71(1):182-6. doi: 10.1073/pnas.71.1.182.
5
Influence of 2'-O-acetylation on the antiviral activity of polyribonucleotides.2'-O-乙酰化对多核糖核苷酸抗病毒活性的影响。
Biochim Biophys Acta. 1972 Mar 14;262(2):227-32. doi: 10.1016/0005-2787(72)90237-7.
6
Antiviral activity of partially thiolated polynucleotides.部分硫醇化多核苷酸的抗病毒活性。
Mol Pharmacol. 1975 Jan;11(1):61-9.
7
Antiviral activity of polynucleotides: role of the 2'-hydroxyl and a pyrimidine 5-methyl.多核苷酸的抗病毒活性:2'-羟基和嘧啶5-甲基的作用。
FEBS Lett. 1972 Jul 15;24(1):137-40. doi: 10.1016/0014-5793(72)80845-7.
8
Polynucleotide displacement reactions: detection by interferon induction.多核苷酸置换反应:通过干扰素诱导进行检测
Biochemistry. 1976 Feb 24;15(4):717-24. doi: 10.1021/bi00649a001.
9
[Biological activity of the polyribonucleotide complex (poly-G)-(poly-C) in relation to the structural characteristics of the original polyribonucleotides].
Vopr Virusol. 1974 Jan-Feb(1):45-9.
10
Mechanism of the antiviral activity resulting from sequential administration of complementary homopolyribonucleotides to cell cultures.向细胞培养物顺序给予互补同聚核糖核苷酸产生抗病毒活性的机制。
J Virol. 1972 May;9(5):721-31. doi: 10.1128/JVI.9.5.721-731.1972.

引用本文的文献

1
Interferon induction: a conformational hypothesis.干扰素诱导:一种构象假说。
Proc Natl Acad Sci U S A. 1979 Mar;76(3):1018-21. doi: 10.1073/pnas.76.3.1018.
2
Inhibition of oncornavirus functions by poly (2-methylthioinosinic acid).聚(2-甲硫基肌苷酸)对肿瘤病毒功能的抑制作用
Nucleic Acids Res. 1975 Dec;2(12):2305-13. doi: 10.1093/nar/2.12.2305.

本文引用的文献

1
A displacement reaction between a polynucleotide Helix and a random coil.
J Mol Biol. 1962 Dec;5:709-17. doi: 10.1016/s0022-2836(62)80097-7.
2
Purification and properties of a potassium-activated phosphodiesterase (RNAase II) from Escherichia coli.来自大肠杆菌的钾激活磷酸二酯酶(核糖核酸酶II)的纯化及特性
Biochemistry. 1965 Jul;4(7):1319-30. doi: 10.1021/bi00883a016.
3
Relationship of biological activities of poly I-poly C to homopolymer molecular weights.聚肌苷酸-聚胞苷酸的生物活性与均聚物分子量的关系。
Nat New Biol. 1971 Sep 8;233(36):52-3. doi: 10.1038/newbio233052a0.
4
Regulation of cellular interferon production: enhancement by antimetabolites.细胞干扰素产生的调节:抗代谢物的增强作用。
Proc Natl Acad Sci U S A. 1970 Sep;67(1):464-71. doi: 10.1073/pnas.67.1.464.
5
Structural requirements of the rI n -rC n complex for induction of human interferon.人干扰素诱导中rI n -rC n复合物的结构要求
J Mol Biol. 1972 Oct 14;70(3):567-87. doi: 10.1016/0022-2836(72)90560-8.
6
Synthesis and properties of poly(2-methylthioinosinic acid).聚(2-甲硫基肌苷酸)的合成与性质
Biochim Biophys Acta. 1972 Apr 26;269(1):27-36. doi: 10.1016/0005-2787(72)90070-6.
7
Interferon required for viral resistance induced by poly I.poly C.聚肌苷酸-聚胞苷酸诱导的病毒抗性所需的干扰素。
Nature. 1970 May 2;226(5244):449-50. doi: 10.1038/226449a0.
8
Antiviral activity of polynucleotides: poly 2'-O-ethyladenylic acid and poly 2'-O-ethyluridylic acid.多核苷酸的抗病毒活性:聚2'-O-乙基腺苷酸和聚2'-O-乙基尿苷酸。
FEBS Lett. 1974 Jun 15;42(3):331-4. doi: 10.1016/0014-5793(74)80758-1.
9
Necessity for the 2'-hydroxyl group for the antiviral activity of synthetic polynucleotides.合成多核苷酸抗病毒活性中2'-羟基的必要性。
J Gen Virol. 1974 Jun;23(3):331-3. doi: 10.1099/0022-1317-23-3-331.
10
Relationship of cytotoxicity and interferon-inducing activity of polyriboinosinic acid. Polyribocytidylic acid to the molecular weights of the homopolymers.
J Gen Virol. 1974 Apr;23(1):83-9. doi: 10.1099/0022-1317-23-1-83.

多核苷酸的抗病毒活性:肌苷酸与2-甲硫基肌苷酸的N2-二甲基鸟苷酸共聚物。

Antiviral activity of polynucleotides: copolymers of inosinic acid and N2-dimethylguanylic of 2-methylthioinosinic acid.

作者信息

De Clercq E, Hattori M, Ikehara M

出版信息

Nucleic Acids Res. 1975 Jan;2(1):121-9. doi: 10.1093/nar/2.1.121.

DOI:10.1093/nar/2.1.121
PMID:165469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC342816/
Abstract

Complexes of poly(C) with copolymers of inosinic acid containing various amounts of mismatched bases (see journal for formula) have been examined for direct resistance to virus infection, interferon induction and toxicity in two different cell cultures (primary rabbit kidney cells and mouse L-929 cells). Complexes in which 20% of the hypoxanthine bases were replaced by (see journal for formula) or ms-2I were partially active whereas complexes in which 40% or more of the hypoxanthine bases were replaced by the odd bases were entirely inactive. The decrease in biological activity observed upon intrusion of (see journal for formula) or ms-2I in the poly(I) strand of poly(I) with poly(C) closely paralleled the amount of odd bases introduced irrespective of the system employed to assess the biological activity (resistance to virus infection, interferon induction or toxicity).

摘要

已对聚(C)与含有不同数量错配碱基的肌苷酸共聚物形成的复合物(化学式见期刊)在两种不同细胞培养物(原代兔肾细胞和小鼠L-929细胞)中进行了病毒感染直接抗性、干扰素诱导和毒性的检测。其中20%的次黄嘌呤碱基被(化学式见期刊)或ms-2I取代的复合物具有部分活性,而40%或更多次黄嘌呤碱基被这些奇碱基取代的复合物则完全无活性。在聚(I)与聚(C)形成的复合物中,当(化学式见期刊)或ms-2I插入聚(I)链时观察到的生物活性下降与引入的奇碱基数量密切相关,无论用于评估生物活性的系统(病毒感染抗性、干扰素诱导或毒性)如何。