ih-RIDME:一种探测异质核环境的脉冲EPR实验。

Q3 Physics and Astronomy
Magnetic resonance (Gottingen, Germany) Pub Date : 2025-03-10 eCollection Date: 2025-01-01 DOI:10.5194/mr-6-93-2025
Sergei Kuzin, Victoriya N Syryamina, Mian Qi, Moritz Fischer, Miriam Hülsmann, Adelheid Godt, Gunnar Jeschke, Maxim Yulikov
{"title":"ih-RIDME:一种探测异质核环境的脉冲EPR实验。","authors":"Sergei Kuzin, Victoriya N Syryamina, Mian Qi, Moritz Fischer, Miriam Hülsmann, Adelheid Godt, Gunnar Jeschke, Maxim Yulikov","doi":"10.5194/mr-6-93-2025","DOIUrl":null,"url":null,"abstract":"<p><p>The intermolecular hyperfine relaxation-induced dipolar modulation enhancement experiment (ih-RIDME) is a pulse electron paramagnetic resonance (EPR) experiment that can be used to probe the properties of a nuclear spin bath in the vicinity of an unpaired electron. The underlying mechanism is the hyperfine spectral diffusion of the electron spin during the mixing block. A quantitative description of the diffusion kinetics being applied to establish the ih-RIDME data model allows one to extend this method to systems with heterogeneous nuclear arrangements assuming a distribution of the local nuclear densities. The heterogeneity can stem from the solvent or the intrinsic nuclei of a structurally flexible (macro)molecule. Therefore, the fitted distribution function can further serve as a method for heterogeneity characterization, quantification and structure-based analysis. Here, we present a detailed introduction to the principles of ih-RIDME application to heterogeneous systems. We discuss the spectral resolution, determination of the spectral diffusion parameters and influence of noise in the experimental data. We further demonstrate the application of the ih-RIDME method to a model spin-labelled macromolecule with unstructured domains. The fitted distribution of local proton densities was reproduced with the help of a conformational ensemble generated using the Monte Carlo approach. Finally, we discuss several pulse sequences exploiting the HYperfine Spectral Diffusion Echo MOdulatioN (HYSDEMON) effect with an improved signal-to-noise ratio.</p>","PeriodicalId":93333,"journal":{"name":"Magnetic resonance (Gottingen, Germany)","volume":"6 1","pages":"93-112"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12247092/pdf/","citationCount":"0","resultStr":"{\"title\":\"ih-RIDME: a pulse EPR experiment to probe the heterogeneous nuclear environment.\",\"authors\":\"Sergei Kuzin, Victoriya N Syryamina, Mian Qi, Moritz Fischer, Miriam Hülsmann, Adelheid Godt, Gunnar Jeschke, Maxim Yulikov\",\"doi\":\"10.5194/mr-6-93-2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The intermolecular hyperfine relaxation-induced dipolar modulation enhancement experiment (ih-RIDME) is a pulse electron paramagnetic resonance (EPR) experiment that can be used to probe the properties of a nuclear spin bath in the vicinity of an unpaired electron. The underlying mechanism is the hyperfine spectral diffusion of the electron spin during the mixing block. A quantitative description of the diffusion kinetics being applied to establish the ih-RIDME data model allows one to extend this method to systems with heterogeneous nuclear arrangements assuming a distribution of the local nuclear densities. The heterogeneity can stem from the solvent or the intrinsic nuclei of a structurally flexible (macro)molecule. Therefore, the fitted distribution function can further serve as a method for heterogeneity characterization, quantification and structure-based analysis. Here, we present a detailed introduction to the principles of ih-RIDME application to heterogeneous systems. We discuss the spectral resolution, determination of the spectral diffusion parameters and influence of noise in the experimental data. We further demonstrate the application of the ih-RIDME method to a model spin-labelled macromolecule with unstructured domains. The fitted distribution of local proton densities was reproduced with the help of a conformational ensemble generated using the Monte Carlo approach. Finally, we discuss several pulse sequences exploiting the HYperfine Spectral Diffusion Echo MOdulatioN (HYSDEMON) effect with an improved signal-to-noise ratio.</p>\",\"PeriodicalId\":93333,\"journal\":{\"name\":\"Magnetic resonance (Gottingen, Germany)\",\"volume\":\"6 1\",\"pages\":\"93-112\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12247092/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Magnetic resonance (Gottingen, Germany)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5194/mr-6-93-2025\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"Physics and Astronomy\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Magnetic resonance (Gottingen, Germany)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5194/mr-6-93-2025","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Physics and Astronomy","Score":null,"Total":0}
引用次数: 0

摘要

分子间超精细弛豫诱导的偶极调制增强实验(ih-RIDME)是一种脉冲电子顺磁共振(EPR)实验,可用于探测未配对电子附近核自旋浴的性质。其基本机制是混合块过程中电子自旋的超精细光谱扩散。用于建立ih-RIDME数据模型的扩散动力学的定量描述允许人们将该方法扩展到具有异质核排列的系统,假设局部核密度分布。这种非均质性可能源于溶剂或结构柔性(宏观)分子的内在核。因此,拟合的分布函数可以进一步作为异质性表征、量化和基于结构的分析方法。在这里,我们详细介绍了ih-RIDME在异构系统中的应用原理。讨论了光谱分辨率、光谱扩散参数的确定以及实验数据中噪声的影响。我们进一步证明了ih-RIDME方法在具有非结构域的自旋标记模型大分子中的应用。利用蒙特卡罗方法生成的构象系综,再现了局部质子密度的拟合分布。最后,我们讨论了几种利用超精细光谱扩散回波调制(HYSDEMON)效应的脉冲序列,这些脉冲序列具有改进的信噪比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ih-RIDME: a pulse EPR experiment to probe the heterogeneous nuclear environment.

The intermolecular hyperfine relaxation-induced dipolar modulation enhancement experiment (ih-RIDME) is a pulse electron paramagnetic resonance (EPR) experiment that can be used to probe the properties of a nuclear spin bath in the vicinity of an unpaired electron. The underlying mechanism is the hyperfine spectral diffusion of the electron spin during the mixing block. A quantitative description of the diffusion kinetics being applied to establish the ih-RIDME data model allows one to extend this method to systems with heterogeneous nuclear arrangements assuming a distribution of the local nuclear densities. The heterogeneity can stem from the solvent or the intrinsic nuclei of a structurally flexible (macro)molecule. Therefore, the fitted distribution function can further serve as a method for heterogeneity characterization, quantification and structure-based analysis. Here, we present a detailed introduction to the principles of ih-RIDME application to heterogeneous systems. We discuss the spectral resolution, determination of the spectral diffusion parameters and influence of noise in the experimental data. We further demonstrate the application of the ih-RIDME method to a model spin-labelled macromolecule with unstructured domains. The fitted distribution of local proton densities was reproduced with the help of a conformational ensemble generated using the Monte Carlo approach. Finally, we discuss several pulse sequences exploiting the HYperfine Spectral Diffusion Echo MOdulatioN (HYSDEMON) effect with an improved signal-to-noise ratio.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.50
自引率
0.00%
发文量
0
审稿时长
14 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信