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Direct and cost-efficient hyperpolarization of long-lived nuclear spin states on universal 15 N 2 -diazirine molecular tags
Author(s) -
Thomas Theis,
Gerardo X. Ortiz,
Angus W. J. Logan,
Kevin Claytor,
Yesu Feng,
William Huhn,
Volker Blüm,
Steven J. Malcolmson,
Eduard Y. Chekmenev,
Qiu Wang,
Warren S. Warren
Publication year - 2016
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1501438
Subject(s) - hyperpolarization (physics) , diazirine , biomolecule , spin isomers of hydrogen , singlet state , nuclear magnetic resonance , polarization (electrochemistry) , spin (aerodynamics) , molecule , chemistry , physics , chemical physics , atomic physics , nanotechnology , nuclear magnetic resonance spectroscopy , materials science , photochemistry , excited state , thermodynamics , organic chemistry , hydrogen
Conventional magnetic resonance (MR) faces serious sensitivity limitations which can be overcome by hyperpolarization methods, but the most common method (dynamic nuclear polarization) is complex and expensive, and applications are limited by short spin lifetimes (typically seconds) of biologically relevant molecules. We use a recently developed method, SABRE-SHEATH, to directly hyperpolarize (15)N2 magnetization and long-lived (15)N2 singlet spin order, with signal decay time constants of 5.8 and 23 minutes, respectively. We find >10,000-fold enhancements generating detectable nuclear MR signals that last for over an hour. (15)N2-diazirines represent a class of particularly promising and versatile molecular tags, and can be incorporated into a wide range of biomolecules without significantly altering molecular function

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