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以氧为中心和以碳为中心的自由基物种的定量³¹P核磁共振检测。

Quantitative 31P NMR detection of oxygen-centered and carbon-centered radical species.

作者信息

Argyropoulos Dimitris S, Li Hongyang, Gaspar Armindo R, Smith Kamilah, Lucia Lucian A, Rojas Orlando J

机构信息

Forest Biomaterials Laboratory, College of Natural Resources, North Carolina State University, Raleigh, NC 27695-8005, USA.

出版信息

Bioorg Med Chem. 2006 Jun 15;14(12):4017-28. doi: 10.1016/j.bmc.2006.02.009. Epub 2006 Feb 28.

Abstract

Quantitative 31P NMR spin trapping techniques can be used as effective tools for the detection and quantification of many free radical species. Free radicals react with a nitroxide phosphorus compound, 5-diisopropoxy-phosphoryl-5-methyl-1-pyrroline-N-oxide (DIPPMPO), to form stable radical adducts, which are suitably detected and accurately quantified using (31)P NMR in the presence of phosphorus containing internal standards. Initially, the 31P NMR signals for the radical adducts of oxygen-centered (OH, O2-) and carbon-centered (*CH3, CH2OH, CH2CH2OH) radicals were assigned. Subsequently, the quantitative reliability of the developed technique was demonstrated under a variety of experimental conditions. The 31P NMR chemical shifts for the hydroxyl and superoxide reaction adducts with DIPPMPO were found to be 25.3, 16.9, and 17.1 ppm (in phosphate buffer), respectively. The 31P NMR chemical shifts for *CH3, *CH2OH, *CH(OH)CH3, and *C(O)CH3 spin adducts were 23.1, 22.6, 27.3, and 30.2 ppm, respectively. Overall, this effort forms the foundations for a targeted understanding of the nature, identity, and mechanisms of radical activity in a variety of biomolecular processes.

摘要

定量³¹P核磁共振自旋捕获技术可作为检测和定量多种自由基种类的有效工具。自由基与一种氮氧化物磷化合物5 - 二异丙氧基磷酰基 - 5 - 甲基 - 1 - 吡咯啉 - N - 氧化物(DIPPMPO)反应,形成稳定的自由基加合物,在含磷内标的存在下,使用³¹P核磁共振对其进行适当检测和准确定量。最初,确定了以氧为中心的自由基(*OH、O₂⁻)和以碳为中心的自由基(*CH₃、CH₂OH、CH₂CH₂OH)的自由基加合物的³¹P核磁共振信号。随后,在各种实验条件下证明了所开发技术的定量可靠性。发现羟基和超氧化物与DIPPMPO反应加合物的³¹P核磁共振化学位移分别为25.3、16.9和17.1 ppm(在磷酸盐缓冲液中)。*CH₃、*CH₂OH、CH(OH)CH₃和C(O)CH₃自旋加合物的³¹P核磁共振化学位移分别为23.1、22.6、27.3和30.2 ppm。总体而言,这项工作为有针对性地理解各种生物分子过程中自由基活性的性质、特征和机制奠定了基础。

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