Literature DB >> 19886687

Higher sensitivity through selective (13)C excitation in solid-state NMR spectroscopy.

Jakob J Lopez1, Christoph Kaiser, Sam Asami, Clemens Glaubitz.   

Abstract

A notable drawback of NMR spectroscopy is its inherently low sensitivity: 95% of the measuring time consists solely of idle delays during which nuclei regain their Boltzmann equilibrium. Here, a strategy for solid-state (13)C NMR experiments is presented that allows the user to acquire spectra in time periods that are notably shorter than previously necessary. Experiments that are band-selective in nature may utilize the cooling potential of unperturbed nuclei to lower the spin temperature of their excited neighbors. As we demonstrate, it becomes possible to replace the recycle delay in a series of scans by a time period during which proton-driven spin diffusion causes relaxation enhancement by a lower spin temperature of adjacent spins (RELOAD). Typically, a duration of approximately 200 ms suffices for this step, and for 1D (13)C NMR experiments, it is shown that the omission of recycle delays (typically of 2 s length) reduces the measuring time substantially. RELOAD is applied to 2D homonuclear (13)C NMR experiments, and it is demonstrated that for experiments in which correlations between (13)C backbone atoms are detected, the measurement time is reduced by a factor of 10 through a time-saving combination of a smaller number of increments in the indirect dimension and RELOAD.

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Year:  2009        PMID: 19886687     DOI: 10.1021/ja904963n

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  6 in total

1.  Perspectives for sensitivity enhancement in proton-detected solid-state NMR of highly deuterated proteins by preserving water magnetization.

Authors:  Veniamin Chevelkov; ShengQi Xiang; Karin Giller; Stefan Becker; Adam Lange; Bernd Reif
Journal:  J Biomol NMR       Date:  2015-01-30       Impact factor: 2.835

2.  A suite of pulse sequences based on multiple sequential acquisitions at one and two radiofrequency channels for solid-state magic-angle spinning NMR studies of proteins.

Authors:  Kshama Sharma; Perunthiruthy K Madhu; Kaustubh R Mote
Journal:  J Biomol NMR       Date:  2016-06-30       Impact factor: 2.835

3.  Determination of structural topology of a membrane protein in lipid bilayers using polarization optimized experiments (POE) for static and MAS solid state NMR spectroscopy.

Authors:  Kaustubh R Mote; T Gopinath; Gianluigi Veglia
Journal:  J Biomol NMR       Date:  2013-08-21       Impact factor: 2.835

4.  Utilizing afterglow magnetization from cross-polarization magic-angle-spinning solid-state NMR spectroscopy to obtain simultaneous heteronuclear multidimensional spectra.

Authors:  James R Banigan; Nathaniel J Traaseth
Journal:  J Phys Chem B       Date:  2012-05-31       Impact factor: 2.991

5.  Paramagnetic doping of a 7TM membrane protein in lipid bilayers by Gd³⁺-complexes for solid-state NMR spectroscopy.

Authors:  Sandra J Ullrich; Soraya Hölper; Clemens Glaubitz
Journal:  J Biomol NMR       Date:  2013-12-04       Impact factor: 2.835

6.  Enhancing NMR Sensitivity of Natural-Abundance Low-γ Nuclei by Ultrafast Magic-Angle-Spinning Solid-State NMR Spectroscopy.

Authors:  Rongchun Zhang; Yitian Chen; Nair Rodriguez-Hornedo; Ayyalusamy Ramamoorthy
Journal:  Chemphyschem       Date:  2016-07-22       Impact factor: 3.102

  6 in total

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