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学術論文

Homonuclear Simplified Preservation of Equivalent Pathways Spectroscopy

MPS-Authors
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Nimerovsky,  Evgeny
Department of NMR Based Structural Biology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

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Becker,  Stefan
Department of NMR Based Structural Biology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

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Andreas,  Loren B.
Department of NMR Based Structural Biology, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;
Research Group of Solid State NMR Spectroscopy-2, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society;

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引用

Nimerovsky, E., Kosteletos, S., Lange, S., Becker, S., Lange, A., & Andreas, L. B. (2024). Homonuclear Simplified Preservation of Equivalent Pathways Spectroscopy. The Journal of Physical Chemistry Letters, 15(24), 6272-6278. doi:10.1021/acs.jpclett.4c00991.


引用: https://hdl.handle.net/21.11116/0000-000F-7910-7
要旨
Recently developed homonuclear transverse mixing optimal control pulses (hTROP) revealed an elegant way to enhance the detected signal in multidimensional magic-angle spinning (MAS) nuclear magnetic resonance experiments. Inspired by their work, we present two homonuclear simplified preservation of equivalent pathways spectroscopy (hSPEPS) sequences for recoupling CA–CO and CA–CB dipolar couplings under fast and ultrafast MAS rates, theoretically enabling a √2 improvement in sensitivity for each indirect dimension. The efficiencies of hSPEPS are evaluated for non-deuterated samples of influenza A M2 and bacterial rhomboid protease GlpG under two different external magnetic fields (600 and 1200 MHz) and MAS rates (55 and 100 kHz). Three-dimensional (H)CA(CO)NH, (H)CO(CA)NH, and (H)CB(CA)NH spectra demonstrate the high robustness of hSPEPS elements to excite carbon–carbon correlations, especially in the (H)CB(CA)NH spectrum, where hSPEPS outperforms the J-based sequence by a factor of, on average, 2.85.