Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1- 13 C]ketoisocaproate.
Isaiah AdelabuMd Raduanul H ChowdhuryShiraz NantogmaClementinah OladunFiroz AhmedLukas StilgenbauerMarianna SadagurskiThomas TheisBoyd M GoodsonEduard Y ChekmenevPublished in: Metabolites (2023)
Efficient 13 C hyperpolarization of ketoisocaproate is demonstrated in natural isotopic abundance and [1- 13 C]enriched forms via SABRE-SHEATH (Signal Amplification By Reversible Exchange in SHield Enables Alignment Transfer to Heteronuclei). Parahydrogen, as the source of nuclear spin order, and ketoisocaproate undergo simultaneous chemical exchange with an Ir-IMes-based hexacoordinate complex in CD 3 OD. SABRE-SHEATH enables spontaneous polarization transfer from parahydrogen-derived hydrides to the 13 C nucleus of transiently bound ketoisocaproate. 13 C polarization values of up to 18% are achieved at the 1- 13 C site in 1 min in the liquid state at 30 mM substrate concentration. The efficient polarization build-up becomes possible due to favorable relaxation dynamics. Specifically, the exponential build-up time constant (14.3 ± 0.6 s) is substantially lower than the corresponding polarization decay time constant (22.8 ± 1.2 s) at the optimum polarization transfer field (0.4 microtesla) and temperature (10 °C). The experiments with natural abundance ketoisocaproate revealed polarization level on the 13 C-2 site of less than 1%-i.e., one order of magnitude lower than that of the 1- 13 C site-which is only partially due to more-efficient relaxation dynamics in sub-microtesla fields. We rationalize the overall much lower 13 C-2 polarization efficiency in part by less favorable catalyst-binding dynamics of the C-2 site. Pilot SABRE experiments at pH 4.0 (acidified sample) versus pH 6.1 (unaltered sodium [1- 13 C]ketoisocaproate) reveal substantial modulation of SABRE-SHEATH processes by pH, warranting future systematic pH titration studies of ketoisocaproate, as well as other structurally similar ketocarboxylate motifs including pyruvate and alpha-ketoglutarate, with the overarching goal of maximizing 13 C polarization levels in these potent molecular probes. Finally, we also report on the pilot post-mortem use of HP [1- 13 C]ketoisocaproate in a euthanized mouse, demonstrating that SABRE-hyperpolarized 13 C contrast agents hold promise for future metabolic studies.