Faculty Opinions recommendation of A set of BEST triple-resonance experiments for time-optimized protein resonance assignment.

2010 ◽  
Author(s):  
Linda Ball ◽  
Victoria Ann Higman
Keyword(s):  
Resonance Assignment ◽  
Triple Resonance ◽  
Triple Resonance Experiments ◽  
Protein Resonance Assignment

Impact of Transverse Relaxation Optimized Spectroscopy (TROSY) on NMR as a technique in structural biology

2000 ◽  
Vol 33 (2) ◽  
pp. 161-197 ◽  
Author(s):  
Konstantin Pervushin
Keyword(s):  
Resonance Assignment ◽  
Structure Determination ◽  
Isotope Labeling ◽  
Molecular Size ◽  
Coupling Constants ◽  
Scalar Coupling ◽  
Triple Resonance ◽  
Single Quantum ◽  
Triple Resonance Experiments ◽  
Transverse Relaxation

1. Transverse relaxation and the molecular size limit in liquid state NMR 1612. TROSY: how does it work? 1632.1 Transverse relaxation in coupled spin systems 1632.2 The TROSY effect, relaxation due to remote protons and 2H isotope labeling 1653. Direct heteronuclear chemical shift correlations 1683.1 Single-Quantum [15N,1H]-TROSY 1683.2 Zero-Quantum [15N,1H]-TROSY 1713.3 Single-Quantum TROSY with aromatic 13C–1H moieties 1764. Resonance assignment and NOE spectroscopy of large biomolecules 1804.1 TROSY-based triple resonance experiments for 13C, 15N and 1HN backbone resonance assignment in uniformly 2H, 13C, 15N labeled proteins 1804.2 TROSY-type NOE spectroscopy 1865. Scalar coupling across hydrogen bonds observed by TROSY 1876. The use of TROSY for measurements of residual dipolar coupling constants 1907. Conclusions 1918. Acknowledgements 1919. References 191The application of nuclear magnetic resonance (NMR) spectroscopy for structure determination of proteins and nucleic acids (Wüthrich, 1986) with molecular mass exceeding 30 kDa is largely constrained by two factors, fast transverse relaxation of spins of interest and complexity of NMR spectra, both of which increase with increasing molecular size (Wagner, 1993b; Clore & Gronenborn, 1997, 1998b; Kay & Gardner, 1997). The good news is that neither of these factors represent a fundamental limit for the application of NMR techniques to protein structure determination in solution (Clore & Gronenborn, 1998a; Wüthrich, 1998; Wider & Wüthrich, 1999). In fact, in the past few years the size limitations imposed by these factors have been pushed up to 50–70 kDa by the use of 13C, 15N and 2H isotope labeling combined with selective reprotonation of individual chemical groups in conjunction with the use of triple-resonance experiments (Bax, 1994; Gardner et al. 1997; Gardner & Kay, 1998) and heteronuclear-resolved NMR (Fesik & Zuiderweg, 1988; Marion et al. 1989a; Otting & Wüthrich, 1990). Among the largest biomolecules whose 3D structure was solved by NMR are the 44 kDa trimeric ectodomain of simian immunodeficiency virus (SIV) gp41 (Caffrey et al. 1998) and 40–60 kDa particles of the elongation initiation factor 4E solubilized in CHAPS micelles (Matsuo et al. 1997; McGuire et al. 1998).

scholarly journals Signs of proton–proton and proton–fluorine spin–spin coupling constants in 2-fluoro-3-methylpyridine. Sigma and pi contributions to coupling in a nitrogen heterocycle

1969 ◽  
Vol 47 (9) ◽  
pp. 1507-1514 ◽  
Author(s):  
T. Schaefer ◽  
S. S. Danyluk ◽  
C. L. Bell
Keyword(s):  
Nitrogen Atom ◽  
Long Range ◽  
Coupling Constants ◽  
Spin Coupling ◽  
Nitrogen Heterocycle ◽  
Triple Resonance ◽  
Triple Resonance Experiments ◽  
Proton Proton ◽  
Spin Coupling Constants ◽  
Spin Spin Coupling

The signs of all proton–proton and proton–fluorine spin–spin coupling constants in 2-fluoro-3-methylpyridine have been determined by double and triple resonance experiments. The signs of the longrange coupling constants, JH,CH3 and JF,CH3 are the same as in fluorotoluene derivatives. Their magnitudes are consistent with the assumption that the nitrogen atom primarily polarizes the σ bonds in the molecule, leaving the π contribution to the long-range coupling relatively unaffected.

Collisional Transfer of Energy in Ammonia; Some Triple Resonance Experiments

1973 ◽  
Vol 28 (10) ◽  
pp. 1703-1706 ◽  
Author(s):  
Harold Jones ◽  
Achim Eyer
Keyword(s):  
Microwave Power ◽  
Triple Resonance ◽  
Population Changes ◽  
Triple Resonance Experiments ◽  
Collisional Transitions

Infrared-microwave-microwave triple resonance experiments in ammonia are reported. The power modulated P13 line of a N2O laser was used to pump the ν2[Q(8,7)] transition of ammonia. The dependance of the intensity of the collisionally induced signals produced at the (7,7), (6,6), (5,5) and (4,4) microwave transitions on c. w. microwave power applied to the (8,7) transition was measured. From the null signal observed for the (7,7) transition when the (8,7) transition was saturated, it was concluded that population changes produced in the (7,7) levels occur predominently via direct collisional transitions which are strongly parity sensitive and that other processes have little contribution. The signals observed for the (6,6), (5,5) and (4,4) are produced by processes which are largely insensitive to parity.

ESR and ENDOR Investigations of Adrenochrome Semiquinone and Related Amino-1,2-Benzosemiquinone Radicals

1985 ◽  
Vol 40 (7-8) ◽  
pp. 531-534 ◽  
Author(s):  
Hartmut B. Stegmann ◽  
Hoang Dao-Ba ◽  
Klaus Scheffler ◽  
Martin G. Peter
Keyword(s):  
Hyperfine Structure ◽  
Spin Density ◽  
Ethanol Solution ◽  
Coupling Constants ◽  
Triple Resonance ◽  
Triple Resonance Experiments ◽  
Proton Coupling ◽  
Endor Spectroscopy ◽  
Nitrogen Coupling

Abstract Dimethyl or diethylamine reacts very smoothly in ethanol solution with catechols to the corresponding aminoquinones. The paramagnetic intermediates, the semiquinones, are investigated by ESR and ENDOR spectroscopy using the spin stabilisation technique with diarylthallium cations. The spectra of these radicals show clearly the thallium and nitrogen coupling and the hydrogen hyperfine structure. For some examples the signs of the proton coupling constants are determined by TRIPLE resonance experiments. The results indicate a negative spin density in one position of the unsymmetrically substituted radical 3. With the results obtained for the monocyclic aminosemiquinones the hyperfine structure of the adrenochrome semiquinone is analysed.

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