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Improved detection of long-range residual dipolar couplings in weakly aligned samples by Lee–Goldburg decoupling of homonuclear dipolar truncation

Abstract

Homonuclear 1H residual dipolar couplings (RDCs) truncate the evolution of transverse 1H magnetization of weakly aligned molecules in high-resolution NMR experiments. This leads to losses in sensitivity or resolution in experiments that require extended 1H evolution times. Lee–Goldburg decoupling schemes have been shown to remove the effects of homonuclear dipolar couplings, while preserving chemical shift evolution in a number of solid-state NMR applications. Here, it is shown that the Lee-Goldburg sequence can be effectively incorporated into INEPT- or HMQC-type transfer schemes in liquid state weak alignment experiments in order to increase the efficiency of the magnetization transfer. The method is applied to the sensitive detection of 1HN13C long-range RDCs in a three-dimensional HCN experiment. As compared to a conventional HCN experiment, an average sensitivity increase by a factor of 2.4 is obtained for a sample of weakly aligned protein G. This makes it possible to detect 170 long-range 1HN13C RDCs for distances up to 4.9 Å

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Correspondence to Stephan Grzesiek.

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Jensen, P., Sass, HJ. & Grzesiek, S. Improved detection of long-range residual dipolar couplings in weakly aligned samples by Lee–Goldburg decoupling of homonuclear dipolar truncation. J Biomol NMR 30, 443–450 (2004). https://doi.org/10.1007/s10858-004-5318-0

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  • DOI: https://doi.org/10.1007/s10858-004-5318-0

Keywords

  • NMR
  • protein
  • structure
  • weak alignment