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来自完整细胞的2-5A及相关寡核苷酸的放射免疫、放射结合和高效液相色谱分析。

Radioimmune, radiobinding and HPLC analysis of 2-5A and related oligonucleotides from intact cells.

作者信息

Knight M, Cayley P J, Silverman R H, Wreschner D H, Gilbert C S, Brown R E, Kerr I M

出版信息

Nature. 1980 Nov 13;288(5787):189-92. doi: 10.1038/288189a0.

Abstract

The enzyme (2-5A synthetase) which synthesizes ppp(A2'p)nA where n=2 to 4 (collectively referred to as 2-5A) is widely distributed in a variety of cells and tissues in amounts which increase response to interferon and vary with growth and hormone status. 2-5A activates a nuclease which inhibits protein synthesis. The non-phosphorylated 'core' of 2-5A ((A2'p)nA, n=2 to 4) can inhibit DNA synthesis and cell growth. Here we describe convenient and sensitive radioimmune (RI) and radiobinding (RB) assays for core and 2-5A. In combination with more satisfactory high performance liquid chromatography (HPCL) methods using reverse-phase C18 columns, these assays have been used to detect core and 2-5A in crude extracts from interferon-treated cells. The novel 2-5A synthetase products NAD2'p5' A2'p5'A and A5'p45'A2'p5'A2'p5'A (ref. 13), which can also be detected using the RB assay, were not found in significant amounts. The natural occurrence of core has not been described previously.

摘要

合成三磷酸腺苷(A2'p)nA(其中n = 2至4,统称为2-5A)的酶(2-5A合成酶)广泛分布于多种细胞和组织中,其含量会随着对干扰素的反应增加而升高,并随生长和激素状态而变化。2-5A激活一种抑制蛋白质合成的核酸酶。2-5A的非磷酸化“核心”((A2'p)nA,n = 2至4)可抑制DNA合成和细胞生长。在此,我们描述了针对核心2-5A的简便且灵敏的放射免疫(RI)和放射结合(RB)测定法。与使用反相C18柱的更令人满意的高效液相色谱(HPCL)方法相结合,这些测定法已用于检测经干扰素处理的细胞粗提物中的核心2-5A。通过RB测定法也可检测到的新型2-5A合成酶产物NAD2'p5'A2'p5'A和A5'p45'A2'p5'A2'p5'A(参考文献13),其含量并不显著。核心2-5A的天然存在此前尚未见报道。

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