4.8 Article

3D TEDOR NMR experiments for the simultaneous measurement of multiple carbon-nitrogen distances in uniformly 13C, 15N-labeled solids

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 124, Issue 36, Pages 10728-10742

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja026385y

Keywords

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Funding

  1. NCRR NIH HHS [RR 00995] Funding Source: Medline
  2. NIGMS NIH HHS [GM 23289, GM 23403] Funding Source: Medline

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We describe three-dimensional magic-angle-spinning NMR experiments for the simultaneous measurement of multiple carbon-nitrogen distances in uniformly C-13,N-15-labeled solids. The approaches employ transferred echo double resonance (TEDOR) for C-13-N-15 coherence transfer and N-15 and C-13 frequency labeling for site-specific resolution, and build on several previous 3D TEDOR techniques. The novel feature of the 3D TEDOR pulse sequences presented here is that they are specifically designed to circumvent the detrimental effects of homonuclear C-13-C-13 J-couplings on the measurement of weak C-13-N-15 dipolar couplings. In particular, homonuclear J-couplings lead to two undesirable effects: (I) they generate anti-phase and multiple-quantum (MQ) spin coherences, which lead to spurious cross-peaks and phase-twisted lines in the 2D N-15-C-13 correlation spectra, and thus degrade the spectral resolution and prohibit the extraction of reliable cross-peak intensities, and (ii) they significantly reduce cross-peak intensities for strongly J-coupled C-13 sites (e.g., CO and C-alpha). The first experiment employs z-filter periods to suppress the anti-phase and MQ coherences and generates 2D spectra with purely absorptive peaks for all TEDOR mixing times. The second approach uses band-selective C-13 pulses to refocus J-couplings between C-13 spins within the selective pulse bandwidth and C-13 spins outside the bandwidth. The internuclear distances are extracted by using a simple analytical model, which accounts explicitly for multiple spin-spin couplings contributing to cross-peak buildup. The experiments are demonstrated in two U-C-13,N-15-labeled peptides, N-acetyl-L-Val-L-Leu (N-ac-VL) and N-formyl-L-Met-L-Leu-L-Phe (N-f-MLF), where 20 and 26 C-13-N-15 distances up to similar to5-6 Angstrom were measured, respectively. Of the measured distances, 10 in N-ac-VL and 13 in N-f-MLF are greater than 3 Angstrom and provide valuable structural constraints.

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