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Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate

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 k...

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Autores principales: Adelabu, Isaiah, Chowdhury, Md Raduanul H., Nantogma, Shiraz, Oladun, Clementinah, Ahmed, Firoz, Stilgenbauer, Lukas, Sadagurski, Marianna, Theis, Thomas, Goodson, Boyd M., Chekmenev, Eduard Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963635/
https://www.ncbi.nlm.nih.gov/pubmed/36837820
http://dx.doi.org/10.3390/metabo13020200
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author Adelabu, Isaiah
Chowdhury, Md Raduanul H.
Nantogma, Shiraz
Oladun, Clementinah
Ahmed, Firoz
Stilgenbauer, Lukas
Sadagurski, Marianna
Theis, Thomas
Goodson, Boyd M.
Chekmenev, Eduard Y.
author_facet Adelabu, Isaiah
Chowdhury, Md Raduanul H.
Nantogma, Shiraz
Oladun, Clementinah
Ahmed, Firoz
Stilgenbauer, Lukas
Sadagurski, Marianna
Theis, Thomas
Goodson, Boyd M.
Chekmenev, Eduard Y.
author_sort Adelabu, Isaiah
collection PubMed
description 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.
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spelling pubmed-99636352023-02-26 Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate Adelabu, Isaiah Chowdhury, Md Raduanul H. Nantogma, Shiraz Oladun, Clementinah Ahmed, Firoz Stilgenbauer, Lukas Sadagurski, Marianna Theis, Thomas Goodson, Boyd M. Chekmenev, Eduard Y. Metabolites Article 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. MDPI 2023-01-29 /pmc/articles/PMC9963635/ /pubmed/36837820 http://dx.doi.org/10.3390/metabo13020200 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Adelabu, Isaiah
Chowdhury, Md Raduanul H.
Nantogma, Shiraz
Oladun, Clementinah
Ahmed, Firoz
Stilgenbauer, Lukas
Sadagurski, Marianna
Theis, Thomas
Goodson, Boyd M.
Chekmenev, Eduard Y.
Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate
title Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate
title_full Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate
title_fullStr Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate
title_full_unstemmed Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate
title_short Efficient SABRE-SHEATH Hyperpolarization of Potent Branched-Chain-Amino-Acid Metabolic Probe [1-(13)C]ketoisocaproate
title_sort efficient sabre-sheath hyperpolarization of potent branched-chain-amino-acid metabolic probe [1-(13)c]ketoisocaproate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963635/
https://www.ncbi.nlm.nih.gov/pubmed/36837820
http://dx.doi.org/10.3390/metabo13020200
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