Evaluation of enzymatic and magnetic properties of γ-glutamyl-[1-13C]glycine and its deuteration toward longer retention of the hyperpolarized state. Issue 59 (17th November 2021)
- Record Type:
- Journal Article
- Title:
- Evaluation of enzymatic and magnetic properties of γ-glutamyl-[1-13C]glycine and its deuteration toward longer retention of the hyperpolarized state. Issue 59 (17th November 2021)
- Main Title:
- Evaluation of enzymatic and magnetic properties of γ-glutamyl-[1-13C]glycine and its deuteration toward longer retention of the hyperpolarized state
- Authors:
- Kondo, Yohei
Saito, Yutaro
Elhelaly, Abdelazim Elsayed
Hyodo, Fuminori
Nishihara, Tatsuya
Itoda, Marino
Nonaka, Hiroshi
Matsuo, Masayuki
Sando, Shinsuke - Abstract:
- Abstract : By examining enzymatic and magnetic properties, γ-Glu-[1- 13 C]Gly- d 2 was developed as a long-lived DNP molecular probe for detecting γ-glutamyl transpeptidase. Abstract : Dynamic nuclear polarization (DNP) is an emerging cutting-edge method of acquiring metabolic and physiological information in vivo . We recently developed γ-glutamyl-[1- 13 C]glycine (γ-Glu-[1- 13 C]Gly) as a DNP nuclear magnetic resonance (NMR) molecular probe to detect γ-glutamyl transpeptidase (GGT) activity in vivo . However, the detailed enzymatic and magnetic properties of this probe remain unknown. Here, we evaluate a γ-Glu–Gly scaffold and develop a deuterated probe, γ-Glu-[1- 13 C]Gly- d 2, that can realize a longer lifetime of the hyperpolarized signal. We initially evaluated the GGT-mediated enzymatic conversion of γ-Glu–Gly and the magnetic properties of 13 C-enriched γ-Glu–Gly (γ-Glu-[1- 13 C]Gly and γ-[5- 13 C]Glu–Gly) to support the validity of γ-Glu-[1- 13 C]Gly as a DNP NMR molecular probe for GGT. We then examined the spin-lattice relaxation time ( T 1 ) of γ-Glu-[1- 13 C]Gly and γ-Glu-[1- 13 C]Gly- d 2 under various conditions (D2 O, PBS, and serum) and confirmed that the T 1 of γ-Glu-[1- 13 C]Gly and γ-Glu-[1- 13 C]Gly- d 2 was maintained for 30 s (9.4 T) and 41 s (9.4 T), respectively, even in serum. Relaxation analysis of γ-Glu-[1- 13 C]Gly revealed a significant contribution of the dipole–dipole interaction and the chemical shift anisotropy relaxation pathway (71% of theAbstract : By examining enzymatic and magnetic properties, γ-Glu-[1- 13 C]Gly- d 2 was developed as a long-lived DNP molecular probe for detecting γ-glutamyl transpeptidase. Abstract : Dynamic nuclear polarization (DNP) is an emerging cutting-edge method of acquiring metabolic and physiological information in vivo . We recently developed γ-glutamyl-[1- 13 C]glycine (γ-Glu-[1- 13 C]Gly) as a DNP nuclear magnetic resonance (NMR) molecular probe to detect γ-glutamyl transpeptidase (GGT) activity in vivo . However, the detailed enzymatic and magnetic properties of this probe remain unknown. Here, we evaluate a γ-Glu–Gly scaffold and develop a deuterated probe, γ-Glu-[1- 13 C]Gly- d 2, that can realize a longer lifetime of the hyperpolarized signal. We initially evaluated the GGT-mediated enzymatic conversion of γ-Glu–Gly and the magnetic properties of 13 C-enriched γ-Glu–Gly (γ-Glu-[1- 13 C]Gly and γ-[5- 13 C]Glu–Gly) to support the validity of γ-Glu-[1- 13 C]Gly as a DNP NMR molecular probe for GGT. We then examined the spin-lattice relaxation time ( T 1 ) of γ-Glu-[1- 13 C]Gly and γ-Glu-[1- 13 C]Gly- d 2 under various conditions (D2 O, PBS, and serum) and confirmed that the T 1 of γ-Glu-[1- 13 C]Gly and γ-Glu-[1- 13 C]Gly- d 2 was maintained for 30 s (9.4 T) and 41 s (9.4 T), respectively, even in serum. Relaxation analysis of γ-Glu-[1- 13 C]Gly revealed a significant contribution of the dipole–dipole interaction and the chemical shift anisotropy relaxation pathway (71% of the total relaxation rate at 9.4 T), indicating the potential of deuteration and the use of a lower magnetic field for realizing a longer T 1 . In fact, by using γ-Glu-[1- 13 C]Gly- d 2 as a DNP probe, we achieved longer retention of the hyperpolarized signal at 1.4 T. … (more)
- Is Part Of:
- RSC advances. Volume 11:Issue 59(2021)
- Journal:
- RSC advances
- Issue:
- Volume 11:Issue 59(2021)
- Issue Display:
- Volume 11, Issue 59 (2021)
- Year:
- 2021
- Volume:
- 11
- Issue:
- 59
- Issue Sort Value:
- 2021-0011-0059-0000
- Page Start:
- 37011
- Page End:
- 37018
- Publication Date:
- 2021-11-17
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1ra07343e ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19989.xml