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利用 APB Northern 印迹分析 Queuosine tRNA 修饰。

Analysis of Queuosine tRNA Modification Using APB Northern Blot Assay.

机构信息

Division of Epigenetics, German Cancer Research Center (DKFZ), Heidelberg, Germany and Faculty of Biosciences, University of Heidelberg, Heidelberg, Germany.

Division of Biochemistry, Mannheim Institute for Innate Immunoscience (MI3), Medical Faculty Mannheim, Heidelberg University, Mannheim, and Center for Molecular Biology of Heidelberg University (ZMBH), Heidelberg, Germany.

出版信息

Methods Mol Biol. 2021;2298:217-230. doi: 10.1007/978-1-0716-1374-0_14.

Abstract

Queuosine (Q) is a hypermodified base that occurs at the wobble position of transfer RNAs (tRNAs) with a GUN anticodon. Q-tRNA modification is widespread among eukaryotes, yet bacteria are the original source of Q. Eukaryotes acquire Q from their diet, or from the gut microbiota (in multicellular organisms). Despite decades of study, the detailed roles of Q-tRNA modification remain to be elucidated, especially regarding its specific mechanisms of action. Here, we describe a method for the fast and reliable detection of Q-tRNA modification levels in individual tRNAs using a few micrograms of total RNA as starting material. The methodology is based on the co-polymerization of boronic acid (N-acryloyl-3-aminophenylboronic acid (APB)) in polyacrylamide gels, and on the interplay between this derivative and free cis-diol groups of the tRNA. During electrophoresis, the cis-diol groups slow down the Q-modified tRNA, which then can be separated from unmodified tRNA and quantified using Northern blot analysis.

摘要

Queuosine (Q) 是一种超修饰碱基,存在于具有 GUN 反密码子的转移 RNA(tRNA)的摆动位置。Q-tRNA 修饰在真核生物中广泛存在,而细菌是 Q 的原始来源。真核生物从饮食中或从肠道微生物群(在多细胞生物中)获得 Q。尽管经过几十年的研究,Q-tRNA 修饰的详细作用仍有待阐明,特别是其特定的作用机制。在这里,我们描述了一种使用少量微克总 RNA 作为起始材料快速可靠地检测单个 tRNA 中 Q-tRNA 修饰水平的方法。该方法基于硼酸(N-丙烯酰基-3-氨基苯硼酸(APB))在聚丙烯酰胺凝胶中的共聚,以及该衍生物与 tRNA 中游离顺式二醇基团之间的相互作用。在电泳过程中,顺式二醇基团会减缓 Q 修饰的 tRNA,然后可以将其与未修饰的 tRNA 分离,并使用 Northern blot 分析进行定量。

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