Magnetization Transfer to Enhance NOE Cross‐Peaks among Labile Protons: Applications to Imino–Imino Sequential Walks in SARS‐CoV‐2‐Derived RNAs
Autor: | Andreas Oxenfarth, Mihajlo Novakovic, Robbin Schnieders, Eriks Kupče, Tali Scherf, Harald Schwalbe, J Tassilo Grün, Julia Wirmer-Bartoschek, Christian Richter, Lucio Frydman |
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Rok vydání: | 2021 |
Předmět: |
2019-20 coronavirus outbreak
2D NMR spectroscopy Resolution (mass spectrometry) Stereochemistry Forschungsartikel Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) NMR Spectroscopy | Very Important Paper 010402 general chemistry 01 natural sciences Catalysis Magnetization transfer Nuclear Magnetic Resonance Biomolecular Research Articles Chemistry SARS-CoV-2 010405 organic chemistry Magnetic Phenomena RNA General Medicine Nuclear magnetic resonance spectroscopy General Chemistry 0104 chemical sciences Nucleic acid RNA Viral Protons Two-dimensional nuclear magnetic resonance spectroscopy CEST Research Article NOESY |
Zdroj: | Angewandte Chemie International Edition Angewandte Chemie (International Ed. in English) Angewandte Chemie (Weinheim an Der Bergstrasse, Germany) |
ISSN: | 1433-7851 |
DOI: | 10.1002/anie.202015948 |
Popis: | 2D NOESY plays a central role in structural NMR spectroscopy. We have recently discussed methods that rely on solvent‐driven exchanges to enhance NOE correlations between exchangeable and non‐exchangeable protons in nucleic acids. Such methods, however, fail when trying to establish connectivities within pools of labile protons. This study introduces an alternative that also enhances NOEs between such labile sites, based on encoding a priori selected peaks by selective saturations. The resulting selective magnetization transfer (SMT) experiment proves particularly useful for enhancing the imino–imino cross‐peaks in RNAs, which is a first step in the NMR resolution of these structures. The origins of these enhancements are discussed, and their potential is demonstrated on RNA fragments derived from the genome of SARS‐CoV‐2, recorded with better sensitivity and an order of magnitude faster than conventional 2D counterparts. An approach to enhance the sensitivity of 2D NOESY correlations among labile protons is introduced and exemplified with experiments on RNA fragments derived from the SARS‐CoV‐2 genome and with other samples. The approach leads to experiments that are ca. 10‐fold faster and 3‐fold more sensitive than conventional counterparts. The mechanism of this sensitivity boost is explained, and its strengths and limitations are analyzed. |
Databáze: | OpenAIRE |
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