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来自大肠杆菌的首个茎环鸟苷-II核糖开关的H、C、N和P化学位移归属

H, C, N and P chemical shift assignment of the first stem-loop Guanidine-II riboswitch from Escherichia coli.

作者信息

Koob Tatjana, Döpp Silas, Schwalbe Harald

机构信息

Institute for Organic Chemistry and Chemical Biology, Johann Wolfgang Goethe-University Frankfurt, Max‑von‑Laue‑Str. 7, 60438, Frankfurt/M, Germany.

Center for Biomolecular Magnetic Resonance (BMRZ), Johann Wolfgang Goethe-University Frankfurt, Max‑von‑Laue‑Str. 9, 60438, Frankfurt/M, Germany.

出版信息

Biomol NMR Assign. 2025 Jun;19(1):53-58. doi: 10.1007/s12104-025-10217-6. Epub 2025 Feb 1.

Abstract

A comprehensive understanding of RNA-based gene regulation is a fundamental aspect for the development of innovative therapeutic options in medicine and for a more targeted response to environmental problems. Within the different mechanisms of RNA-based gene regulation, riboswitches are particularly interesting as they change their structure in response to the interaction with a low molecular weight ligand, often a well-known metabolite. Four distinct classes of riboswitches recognize the very small guanidinium cation. We are focused on the Guanidine-II riboswitch with the mini-ykkC motif. We report here the assignment of the H, C, N and P chemical shifts of the 23 nucleotide-long sequence of the first stem-loop of the Guanidine-II riboswitch aptamer from Escherichia coli. Despite its small size, the assignment of the NMR signals of this RNA proved to be challenging as it has symmetrical base pairs and palindromic character.

摘要

全面理解基于RNA的基因调控是医学中开发创新治疗方案以及更有针对性地应对环境问题的一个基本方面。在基于RNA的基因调控的不同机制中,核糖开关特别有趣,因为它们会根据与低分子量配体(通常是一种知名代谢物)的相互作用而改变其结构。四类不同的核糖开关识别非常小的胍阳离子。我们专注于具有mini-ykkC基序的胍-II核糖开关。我们在此报告了来自大肠杆菌的胍-II核糖开关适体第一个茎环23个核苷酸长序列的H、C、N和P化学位移的归属。尽管其尺寸较小,但该RNA的NMR信号归属却具有挑战性,因为它具有对称碱基对和回文特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2e6/12117010/b8a0e536c676/12104_2025_10217_Fig1_HTML.jpg

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