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多核苷酸诱导干扰素:结构-功能关系

Interferon induction by polynucleotides: structure-function relationship.

作者信息

De Clercq E

出版信息

Tex Rep Biol Med. 1977;35:29-38.

PMID:358456
Abstract

In view of recent developments, the structural determinants of the interferon inducing activity of polynucleotides have been (re)evaluated. To induce interferon, the polynucleotide should be sufficiently large and double-stranded, although not necessarily double-stranded over its whole length. It should be sufficiently stable to both thermal denaturation and hydrolysis by nucleases. It should also contain a particular steric conformation. This conformation is most regularly ensured by the presence of 2'-hydroxyl in the ribose moieties and intact purine-pyrimidine base pairs in the interior of the double helix. Other biologic activities of polynucleotides, such as anti-complement activity and inhibition of reverse transcriptase (RNA-directed DNA polymerase) activity, depend on structural requirements which are rather antagonistic to those governing the interferon response.

摘要

鉴于最近的研究进展,人们对多核苷酸诱导干扰素活性的结构决定因素进行了(重新)评估。为了诱导干扰素,多核苷酸应足够大且为双链,尽管不一定在其整个长度上都是双链。它应具有足够的稳定性,以抵抗热变性和核酸酶的水解。它还应包含特定的空间构象。这种构象最常通过核糖部分中2'-羟基的存在以及双螺旋内部完整的嘌呤-嘧啶碱基对来确保。多核苷酸的其他生物活性,如抗补体活性和逆转录酶(RNA指导的DNA聚合酶)活性的抑制,取决于与控制干扰素反应的结构要求相当对立的结构要求。

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