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Göbl, C.* ; Madl, T. ; Simon, B.* ; Sattler, M.

NMR approaches for structural analysis of multidomain proteins and complexes in solution.

Prog. Nucl. Magn. Reson. Spectrosc. 80, 26-63 (2014)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
NMR spectroscopy is a key method for studying the structure and dynamics of (large) multidomain proteins and complexes in solution. It plays a unique role in integrated structural biology approaches as especially information about conformational dynamics can be readily obtained at residue resolution. Here, we review NMR techniques for such studies focusing on state-of-the-art tools and practical aspects. An efficient approach for determining the quaternary structure of multidomain complexes starts from the structures of individual domains or subunits. The arrangement of the domains/subunits within the complex is then defined based on NMR measurements that provide information about the domain interfaces combined with (long-range) distance and orientational restraints. Aspects discussed include sample preparation, specific isotope labeling and spin labeling; determination of binding interfaces and domain/subunit arrangements from chemical shift perturbations (CSP), nuclear Overhauser effects (NOEs), isotope editing/filtering, cross-saturation, and differential line broadening; and based on paramagnetic relaxation enhancements (PRE) using covalent and soluble spin labels. Finally, the utility of complementary methods such as small-angle X-ray or neutron scattering (SAXS, SANS), electron paramagnetic resonance (EPR) or fluorescence spectroscopy techniques is discussed. The applications of NMR techniques are illustrated with studies of challenging (high molecular weight) protein complexes.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Integrated Structural Biology ; Multidomain Proteins ; Nmr Methods ; Paramagnetic Relaxation Enhancements ; Protein Complexes; Residual Dipolar Couplings; Nuclear-magnetic-resonance; Molecular-weight Proteins; X-ray-scattering; Paramagnetic Relaxation Enhancement; Small-angle Scattering; Model-free Approach; Rotational Diffusion Anisotropy; N-terminal Domain; Malate-synthase-g
Sprache englisch
Veröffentlichungsjahr 2014
HGF-Berichtsjahr 2014
ISSN (print) / ISBN 0079-6565
e-ISSN 1873-3301
Zeitschrift Progress in Nuclear Magnetic Resonance Spectroscopy
Quellenangaben Band: 80, Heft: , Seiten: 26-63 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort Oxford
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Structural Biology (STB)
POF Topic(s) 30203 - Molecular Targets and Therapies
30505 - New Technologies for Biomedical Discoveries
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-503000-001
G-552800-001
PubMed ID 24924266
DOI 10.1016/j.pnmrs.2014.05.003
WOS ID WOS:000338820800003
Scopus ID 84901800224
Erfassungsdatum 2014-06-15
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