77Se核的溶解动力学核极化

IF 3.4 Q2 CHEMISTRY, ANALYTICAL Analysis & sensing Pub Date : 2022-10-31 DOI:10.1002/anse.202200086
Dr. Eul Hyun Suh, Dr. James Ratnakar, Dr. Jaspal Singh, Prof. Zoltan Kovacs
{"title":"77Se核的溶解动力学核极化","authors":"Dr. Eul Hyun Suh,&nbsp;Dr. James Ratnakar,&nbsp;Dr. Jaspal Singh,&nbsp;Prof. Zoltan Kovacs","doi":"10.1002/anse.202200086","DOIUrl":null,"url":null,"abstract":"<p><sup>77</sup>Se is a spin <math>\n \n <semantics>\n \n <mrow>\n <mn>1</mn>\n <mo>/</mo>\n <mn>2</mn>\n </mrow>\n \n <annotation>\n ${{ 1/2 }}$\n</annotation>\n </semantics>\n </math>\n, low sensitivity nucleus with a natural abundance of 7.6 %. Although <sup>77</sup>Se NMR is very useful in the characterization of selenium containing molecules including seleno-proteins, the detection of <sup>77</sup>Se is challenging in biological samples without enrichment. Therefore, the goal of this work was to establish whether the <sup>77</sup>Se signal could be enhanced in the liquid state by dissolution dynamic nuclear polarization (DNP) NMR without the need of enrichment. The dominant spin-lattice relaxation mechanism for <sup>77</sup>Se is via chemical shift anisotropy, which is highly dependent on the molecular symmetry. Here we tested three selenium compounds (sodium selenate, sodium selenite and selenocystine) with different molecular symmetries in dissolution DNP experiments and demonstrated that <sup>77</sup>Se DNP using commercially available hardware is feasible but the achieved NMR signal enhancements (1368-fold for selenate, 125-fold for selenite and no enhancement for selenocystine at 9.4 T) were strongly dependent on molecular symmetry.</p>","PeriodicalId":72192,"journal":{"name":"Analysis & sensing","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2022-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dissolution Dynamic Nuclear Polarization of the 77Se Nucleus\",\"authors\":\"Dr. Eul Hyun Suh,&nbsp;Dr. James Ratnakar,&nbsp;Dr. Jaspal Singh,&nbsp;Prof. Zoltan Kovacs\",\"doi\":\"10.1002/anse.202200086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><sup>77</sup>Se is a spin <math>\\n \\n <semantics>\\n \\n <mrow>\\n <mn>1</mn>\\n <mo>/</mo>\\n <mn>2</mn>\\n </mrow>\\n \\n <annotation>\\n ${{ 1/2 }}$\\n</annotation>\\n </semantics>\\n </math>\\n, low sensitivity nucleus with a natural abundance of 7.6 %. Although <sup>77</sup>Se NMR is very useful in the characterization of selenium containing molecules including seleno-proteins, the detection of <sup>77</sup>Se is challenging in biological samples without enrichment. Therefore, the goal of this work was to establish whether the <sup>77</sup>Se signal could be enhanced in the liquid state by dissolution dynamic nuclear polarization (DNP) NMR without the need of enrichment. The dominant spin-lattice relaxation mechanism for <sup>77</sup>Se is via chemical shift anisotropy, which is highly dependent on the molecular symmetry. Here we tested three selenium compounds (sodium selenate, sodium selenite and selenocystine) with different molecular symmetries in dissolution DNP experiments and demonstrated that <sup>77</sup>Se DNP using commercially available hardware is feasible but the achieved NMR signal enhancements (1368-fold for selenate, 125-fold for selenite and no enhancement for selenocystine at 9.4 T) were strongly dependent on molecular symmetry.</p>\",\"PeriodicalId\":72192,\"journal\":{\"name\":\"Analysis & sensing\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2022-10-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analysis & sensing\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/anse.202200086\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analysis & sensing","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anse.202200086","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

77Se是一个自旋为1/2${{1/2}$的低灵敏度原子核,自然丰度为7.6 %. 尽管77Se NMR在包括硒蛋白在内的含硒分子的表征中非常有用,但在没有富集的生物样品中检测77Se是具有挑战性的。因此,这项工作的目标是确定在不需要富集的情况下,是否可以通过溶解动态核极化(DNP)NMR在液态下增强77Se信号。77Se的主要自旋晶格弛豫机制是通过化学位移各向异性,这高度依赖于分子对称性。在这里,我们在溶解DNP实验中测试了三种具有不同分子对称性的硒化合物(硒酸钠、亚硒酸钠和硒代胱氨酸),并证明使用市售硬件的77Se DNP是可行的,但在9.4时实现了NMR信号增强(硒酸盐1368倍,亚硒酸盐125倍,硒代胱胺没有增强 T) 强烈依赖于分子对称性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Dissolution Dynamic Nuclear Polarization of the 77Se Nucleus

77Se is a spin 1 / 2 ${{ 1/2 }}$ , low sensitivity nucleus with a natural abundance of 7.6 %. Although 77Se NMR is very useful in the characterization of selenium containing molecules including seleno-proteins, the detection of 77Se is challenging in biological samples without enrichment. Therefore, the goal of this work was to establish whether the 77Se signal could be enhanced in the liquid state by dissolution dynamic nuclear polarization (DNP) NMR without the need of enrichment. The dominant spin-lattice relaxation mechanism for 77Se is via chemical shift anisotropy, which is highly dependent on the molecular symmetry. Here we tested three selenium compounds (sodium selenate, sodium selenite and selenocystine) with different molecular symmetries in dissolution DNP experiments and demonstrated that 77Se DNP using commercially available hardware is feasible but the achieved NMR signal enhancements (1368-fold for selenate, 125-fold for selenite and no enhancement for selenocystine at 9.4 T) were strongly dependent on molecular symmetry.

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
2.60
自引率
0.00%
发文量
0
期刊最新文献
Front Cover: Anal. Sens. 5/2024) Pioneering Sensing Technologies Using Borophene-Based Composite/Hybrid Electrochemical Biosensors for Health Monitoring: A Perspective Front Cover: (Anal. Sens. 4/2024) Biomarker Multiplexing with Rational Design of Nucleic Acid Probe Complex Unimolecular Cucurbit[7]uril-Based Indicator Displacement Assay with Dual Signal-Readout for the Detection of Drugs
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1