Crossref journal-article
Cambridge University Press (CUP)
Quarterly Reviews of Biophysics (56)
Abstract

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).

Bibliography

Pervushin, K. (2000). Impact of Transverse Relaxation Optimized Spectroscopy (TROSY) on NMR as a technique in structural biology. Quarterly Reviews of Biophysics, 33(2), 161–197.

Authors 1
  1. Konstantin Pervushin (first)
References 0 Referenced 141

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Dates
Type When
Created 23 years, 1 month ago (July 27, 2002, 9:36 a.m.)
Deposited 6 years, 5 months ago (March 29, 2019, 3 p.m.)
Indexed 1 month, 4 weeks ago (July 7, 2025, 8:04 a.m.)
Issued 25 years, 4 months ago (May 1, 2000)
Published 25 years, 4 months ago (May 1, 2000)
Published Online 24 years, 7 months ago (Jan. 16, 2001)
Published Print 25 years, 4 months ago (May 1, 2000)
Funders 0

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@article{Pervushin_2000, title={Impact of Transverse Relaxation Optimized Spectroscopy (TROSY) on NMR as a technique in structural biology}, volume={33}, ISSN={1469-8994}, url={http://dx.doi.org/10.1017/s0033583500003619}, DOI={10.1017/s0033583500003619}, number={2}, journal={Quarterly Reviews of Biophysics}, publisher={Cambridge University Press (CUP)}, author={Pervushin, Konstantin}, year={2000}, month=may, pages={161–197} }