实时核磁共振检测使用超极化[1-13C]酸盐的酶活动
James Eills1, Eleonora Cavallari2, Carla Carrera3
1Helmholtz Institute , Johannes Gutenberg University of Mainz , Mainz 55099 , Germany.
Journal of the American Chemical Society
|November 26, 2019
概括
研究人员开发了一种更快,更便宜的方法,使用对诱导极化 (PHIP) 来产生超极化[1-13C] fumarate. 这项技术可以实时进行体内代谢成像,加速使用烟酸作为生物标志物的临床前研究.
科学领域:
- 磁共振成像技术
- 代谢成像
- 生物标志物开发
背景情况:
- 超极化烟酸是使用碳-13磁共振成像进行实时体内代谢的关键探针.
- 目前的生产方法,如溶解动态核极化,
- 假诱导极化 (PHIP) 提供了一个潜在的更容易获得的替代方案.
研究的目的:
- 使用PHIP开发一种高效且快速的超极化[1-13C]酸盐生产方法.
- 为了证明PHIP生成的高极化烟酸对跟踪细胞代谢的有用性.
- 确定烟酸作为一个加速的临床前生物标志物.
主要方法:
- 通过在水中使用商业催化剂对[1-13C]乙二酸进行转.
- 通过恒定电场循环将质子极化转换为C磁化.
- 在细胞悬浮中注射高极化[1-13C] fumarate以进行代谢跟踪.
主要成果:
- 超极化酸产量为89%,而酸作为副产品产量为11%.
- 通过使用86%缩气实现了24%的高极化水平.
- 在细胞悬浮剂中成功跟踪烟酸代谢.
结论:
- PHIP提供了一种高效和经济的途径,
- 这种方法显著加快了代谢研究中的超极化烟酸盐的产生.
- 这些发现为使用基于烟酸的代谢成像的快速临床前研究铺平了道路.
相关概念视频
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
1.6K
When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
1.6K
¹³C NMR: ¹H–¹³C Decoupling
1.6K
The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
1.6K
Other Nuclides: 31P, 19F, 15N NMR
696
Many organic, inorganic, and biological molecules contain spin-half nuclei such as nitrogen-15, fluorine-19, and phosphorus-31. As a result, NMR studies of these nuclei have found extensive applications in chemical and biological research.
While fluorine-19 and phosphorous-31 have high natural abundances (100%) and positive gyromagnetic ratios, nitrogen-15 has a low natural abundance and a negative gyromagnetic ratio. However, nitrogen-15 is still preferred over nitrogen-14 (which has a...
While fluorine-19 and phosphorous-31 have high natural abundances (100%) and positive gyromagnetic ratios, nitrogen-15 has a low natural abundance and a negative gyromagnetic ratio. However, nitrogen-15 is still preferred over nitrogen-14 (which has a...
696
Carbon-13 (¹³C) NMR: Overview
7.5K
Carbon-13 is a naturally occurring NMR-active isotope of carbon with a low natural abundance of 1.1%. In contrast, carbon-12 is the most abundant isotope of carbon with zero nuclear spin. Therefore, it is NMR inactive. The gyromagnetic ratio of carbon-13 is smaller than that of protons. As a result, carbon-13 resonance is about 6000 times weaker than proton resonance. For a given magnetic field strength, the resonance frequency of carbon-13 is about one-fourth of the resonance frequency for...
7.5K
Double Resonance Techniques: Overview
644
Double resonance techniques in Nuclear Magnetic Resonance (NMR) spectroscopy involve the simultaneous application of two different frequencies or radiofrequency pulses to manipulate and observe two distinct nuclear spins. One important application of double resonance is spin decoupling, which selectively suppresses coupling with one type of nucleus while observing the NMR signal from another nucleus, simplifying the spectrum and enhancing resolution.
Spin decoupling is usually achieved by...
Spin decoupling is usually achieved by...
644


