Room-temperature dynamic nuclear polarization enhanced NMR spectroscopy of small biological molecules in water

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作者
Danhua Dai
Xianwei Wang
Yiwei Liu
Xiao-Liang Yang
Clemens Glaubitz
Vasyl Denysenkov
Xiao He
Thomas Prisner
Jiafei Mao
机构
[1] Goethe University Frankfurt,Institute of Physical and Theoretical Chemistry
[2] Goethe University Frankfurt,Center for Biomolecular Magnetic Resonance
[3] East China Normal University,Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering
[4] Zhejiang University of Technology,College of Science
[5] Nanjing University,Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering
[6] Nanjing University,State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering
[7] Goethe University Frankfurt,Institute of Biophysical Chemistry
[8] NYU-ECNU Center for Computational Chemistry at NYU Shanghai,undefined
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Nature Communications | / 12卷
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摘要
Nuclear magnetic resonance (NMR) spectroscopy is a powerful and popular technique for probing the molecular structures, dynamics and chemical properties. However the conventional NMR spectroscopy is bottlenecked by its low sensitivity. Dynamic nuclear polarization (DNP) boosts NMR sensitivity by orders of magnitude and resolves this limitation. In liquid-state this revolutionizing technique has been restricted to a few specific non-biological model molecules in organic solvents. Here we show that the carbon polarization in small biological molecules, including carbohydrates and amino acids, can be enhanced sizably by in situ Overhauser DNP (ODNP) in water at room temperature and at high magnetic field. An observed connection between ODNP 13C enhancement factor and paramagnetic 13C NMR shift has led to the exploration of biologically relevant heterocyclic compound indole. The QM/MM MD simulation underscores the dynamics of intermolecular hydrogen bonds as the driving force for the scalar ODNP in a long-living radical-substrate complex. Our work reconciles results obtained by DNP spectroscopy, paramagnetic NMR and computational chemistry and provides new mechanistic insights into the high-field scalar ODNP.
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