Improved TROSY-HNCA experiment with suppression of conformational exchange induced relaxation |
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Authors: | Konstantin Pervushin Veniamin Gallius Christiane Ritter |
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Affiliation: | (1) Laboratorium für Physikalische Chemie, Switzerland;(2) Eidgenössische Technische Hochschule Hönggerberg, Institute of Biochemistry, CH-8092 Zürich, Switzerland |
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Abstract: | A general method for improving of the sensitivity of the TROSY-type triple resonance experiments in the presence of conformational exchange-induced (CSX) relaxation is proposed based on the use of CPMG-INEPT (Müller et al., J. Am. Chem. Soc., 1995, 117, 11043–11048) during the N–C polarization transfer periods. Significantly improved sensitivity is demonstrated for the majority of cross-peaks in the new [15N,1H]-TROSY-XY-HNCA experiment, measured with partially folded RNase AS-Protein, with negligible loss of sensitivity for resonances unaffected by CSX relaxation. In addition, a comparison of cross-peak amplitudes in [15N,1N]-TROSY-XY-HNCA and conventional [15N,1H]-TROSY-HNCA spectra provides a quick and sensitive estimation of the CSX relaxation contribution. |
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Keywords: | conformational exhange CPMG-INEPT RNase AS-Protein TROSY XY16 |
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