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在缺少大激活模块的情况下,生物源三胺和四胺激活了嗜热四膜虫I组核酶的核心催化能力。

Biogenic triamine and tetraamine activate core catalytic ability of Tetrahymena group I ribozyme in the absence of its large activator module.

作者信息

Gulshan Mst Ara, Rahman Md Motiar, Matsumura Shigeyoshi, Higuchi Tsunehiko, Umezawa Naoki, Ikawa Yoshiya

机构信息

Department of Chemistry, Graduate School of Science and Engineering, University of Toyama, Gofuku 3190, Toyama, 930-8555, Japan; Graduate School of Innovative Life Science, University of Toyama, Gofuku 3190, Toyama, 930-8555, Japan.

Department of Chemistry, Graduate School of Science and Engineering, University of Toyama, Gofuku 3190, Toyama, 930-8555, Japan.

出版信息

Biochem Biophys Res Commun. 2018 Feb 5;496(2):594-600. doi: 10.1016/j.bbrc.2018.01.085. Epub 2018 Jan 12.

Abstract

Group I intron ribozymes share common core elements that form a three-dimensional structure responsible for their catalytic activity. This core structure is unstable without assistance from additional factors that stabilize its tertiary structure. We examined biogenic triamine and tetraamine and also their fragments for their abilities to stabilize a structurally unstable group I ribozyme, ΔP5 ribozyme, derived from the Tetrahymena group I intron ribozyme by deleting its large activator module. Biogenic triamine (spermidine) and tetraamine (spermine) efficiently activated the ΔP5 ribozyme under conditions where the ribozyme was virtually inactive. These observations suggested that polyamines are promising small molecule modulators to activate and possibly inhibit the core catalytic ability of group I ribozymes.

摘要

I 组内含子核酶具有共同的核心元件,这些元件形成一种三维结构,负责其催化活性。在没有其他稳定其三级结构的因子的协助下,这种核心结构是不稳定的。我们研究了生物源三胺和四胺及其片段稳定一种结构不稳定的 I 组核酶(ΔP5 核酶)的能力,该核酶是通过删除其大型激活模块从嗜热四膜虫 I 组内含子核酶衍生而来的。生物源三胺(亚精胺)和四胺(精胺)在核酶几乎无活性的条件下有效地激活了 ΔP5 核酶。这些观察结果表明,多胺有望成为激活并可能抑制 I 组核酶核心催化能力的小分子调节剂。

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