Integrative Biosciences, Department of Chemistry Karmanos Cancer Institute, Wayne State University, 5101 Cass Ave, Detroit, MI, 48202, USA.
Department of Chemistry, North Carolina State University, Raleigh, North Carolina, 27695-8204, USA.
Chemphyschem. 2022 Jan 19;23(2):e202100839. doi: 10.1002/cphc.202100839. Epub 2021 Dec 9.
Signal Amplification By Reversible Exchange in SHield Enabled Alignment Transfer (SABRE-SHEATH) is investigated to achieve rapid hyperpolarization of C spins of [1- C]pyruvate, using parahydrogen as the source of nuclear spin order. Pyruvate exchange with an iridium polarization transfer complex can be modulated via a sensitive interplay between temperature and co-ligation of DMSO and H O. Order-unity C (>50 %) polarization of catalyst-bound [1- C]pyruvate is achieved in less than 30 s by restricting the chemical exchange of [1- C]pyruvate at lower temperatures. On the catalyst bound pyruvate, 39 % polarization is measured using a 1.4 T NMR spectrometer, and extrapolated to >50 % at the end of build-up in situ. The highest measured polarization of a 30-mM pyruvate sample, including free and bound pyruvate is 13 % when using 20 mM DMSO and 0.5 M water in CD OD. Efficient C polarization is also enabled by favorable relaxation dynamics in sub-microtesla magnetic fields, as indicated by fast polarization buildup rates compared to the T spin-relaxation rates (e. g., ∼0.2 s versus ∼0.1 s , respectively, for a 6 mM catalyst-[1- C]pyruvate sample). Finally, the catalyst-bound hyperpolarized [1- C]pyruvate can be released rapidly by cycling the temperature and/or by optimizing the amount of water, paving the way to future biomedical applications of hyperpolarized [1- C]pyruvate produced via comparatively fast and simple SABRE-SHEATH-based approaches.
在屏蔽交换增强对齐转移(SABRE-SHEATH)的作用下,通过将 parahydrogen 作为核自旋序的来源,研究了信号放大,以实现 [1-13C]丙酮酸的 C 自旋的快速极化。通过温度和 DMSO 与 H2O 的共配位之间的敏感相互作用,可以调节丙酮酸与铱极化转移配合物的交换。通过在较低温度下限制 [1-13C]丙酮酸的化学交换,在不到 30s 的时间内实现了催化剂结合的 [1-13C]丙酮酸的 C 大于 50%的有序性(order-unity)极化。在催化剂结合的丙酮酸上,使用 1.4T NMR 光谱仪测量到 39%的极化率,并在原位积累结束时外推到 >50%。在包括游离和结合的丙酮酸的 30mM 丙酮酸样品中,当使用 20mM DMSO 和 0.5M CD3OD 时,测量到的最高极化率为 13%。在亚微特斯拉磁场中,有利的弛豫动力学也能实现有效的 C 极化,这表现为与 T 自旋弛豫率相比,极化快速积累速率更快(例如,对于 6mM 催化剂-[1-13C]丙酮酸样品,分别为 0.2s 与 0.1s)。最后,通过循环温度和/或优化水的量,可以快速释放催化剂结合的高极化 [1-13C]丙酮酸,为未来基于 SABRE-SHEATH 的相对快速和简单方法生产的高极化 [1-13C]丙酮酸的生物医学应用铺平了道路。