基于自旋继电器脉冲sabre -鞘的[15N3]甲硝唑抗生素高效15N超极化

IF 2.624
Shiraz Nantogma , Shannon L. Eriksson , Thomas Theis , Warren S. Warren , Boyd M. Goodson , Eduard Y. Chekmenev
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引用次数: 0

摘要

在微特斯拉磁场中,对氢和待超极化分子在极化转移催化剂的金属中心上同时交换,从而实现了一种核磁共振超极化技术。直到最近,这种方法已经被理解为通过在对氢衍生的氢化物(作为超极化源)和底物的核自旋之间建立水平反交叉来实现超极化。最近,预测应用高度非直观的脉冲序列(包括微特斯拉直流场脉冲)比规范的(静态场)SABRE-SHEATH方法更有效地超极化核自旋。本研究表明,通过使用矩形微特斯拉脉冲的基本“开-关”脉冲序列,可以提高[15N3]甲硝唑的SABRE-SHEATH的超极化效率,[15N3]甲硝唑是fda批准的抗生素(非富集和非超极化形式)和潜在的缺氧传感分子。具体来说,我们证明了在含有20 mM [15N3]甲硝唑的溶液中,对氢鼓泡80秒内可以获得18.5%的15N极化。在实践中,与静态场技术相比,脉冲法获得了(1.32±0.14)倍的P15N改善。这些结果表明,脉冲SABRE-SHEATH成功地应用于15n标记的生物相关分子。此外,我们还证明,虽然脉冲sabre -鞘序列被设计用于从对氢衍生氢化物到甲硝唑的15N催化结合位点的极化转移,但[15N3]甲硝唑的所有三个15N位点都达到了超极化状态。自旋-自旋j型耦合建立的15N中继网络使这种自旋中继极化转移成为可能。本文首次证明了脉冲SABRE-SHEATH(与之前报道的静态场SABRE-SHEATH相反)自旋中继极化转移的可行性,为该技术的广泛应用铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficient 15N hyperpolarization of [15N3]metronidazole antibiotic via spin-relayed pulsed SABRE-SHEATH

Efficient 15N hyperpolarization of [15N3]metronidazole antibiotic via spin-relayed pulsed SABRE-SHEATH
Signal Amplification by Reversible Exchange in SHield Enables Alignment Transfer to Heteronuclei (SABRE-SHEATH) is an NMR hyperpolarization technique that relies of the simultaneous exchange of parahydrogen and a to-be-hyperpolarized molecule on the metal center of a polarization-transfer catalyst in a microtesla magnetic field. Until recently, this method has been understood to perform hyperpolarization by establishing level anti-crossings between the nuclear spins of the parahydrogen derived hydrides (acting as a source of hyperpolarization) and those of the substrate. Recently, the application of highly non-intuitive pulse sequences (comprising pulses of microtesla DC fields) was predicted to hyperpolarize nuclear spins more efficiently than the canonical (static-field) SABRE-SHEATH approach. Here we show that by employing a basic “on-off” pulse sequence of rectangular microtesla pulses, it is possible to improve the hyperpolarization efficiency for SABRE-SHEATH of [15N3]metronidazole, an FDA-approved antibiotic (in non-enriched and non-hyperpolarized form) and potential hypoxia sensing molecule. Specifically, we demonstrate that 15N polarization of 18.5 % can be obtained in 80 s of parahydrogen bubbling parahydrogen through a solution containing 20 mM [15N3]metronidazole. In practice, (1.32 ± 0.14)-fold improvements in P15N was obtained with the pulsed method described here compared to static field technique variant. These results show that pulsed SABRE-SHEATH was successfully applied to 15N-labeled biologically relevant molecule. Moreover, we also demonstrate that although the pulsed SABRE-SHEATH sequence was designed for polarization transfer from parahydrogen derived hydrides to the metronidazole’s 15N catalyst-binding site, all three 15N sites of [15N3]metronidazole attained the hyperpolarized state. This spin-relayed polarization transfer becomes possible due to the 15N relay network established by their spin-spin J-couplings. The feasibility of the spin-relayed polarization transfer is demonstrated here for the first time for pulsed SABRE-SHEATH (as opposed to the static-field SABRE-SHEATH reported previously) and it paves the way to broad applicability of the technique.
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