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Increasing the chemical-shift dispersion of unstructured proteins with a covalent lanthanide shift reagent.
Angew. Chem.-Int. Edit. 55, 14847-14851 (2016)
The study of intrinsically disordered proteins (IDPs) by NMR often suffers from highly overlapped resonances that prevent unambiguous chemical-shift assignments, and data analysis that relies on well-separated resonances. We present a covalent paramagnetic lanthanide-binding tag (LBT) for increasing the chemical-shift dispersion and facilitating the chemical-shift assignment of challenging, repeat-containing IDPs. Linkage of the DOTA-based LBT to a cysteine residue induces pseudo-contact shifts (PCS) for resonances more than 20 residues from the spin-labeling site. This leads to increased chemical-shift dispersion and decreased signal overlap, thereby greatly facilitating chemical-shift assignment. This approach is applicable to IDPs of varying sizes and complexity, and is particularly helpful for repeat-containing IDPs and low-complexity regions. This results in improved efficiency for IDP analysis and binding studies.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
11.709
2.178
15
21
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Nmr ; Chemical-shift Dispersion ; Intrinsically Disordered Proteins ; Lanthanides ; Pseudo-contact Shifts; Intrinsically Disordered Proteins; Backbone Resonance Assignment; Nmr-spectroscopy; Unfolded Proteins; Biomolecular Nmr; Low-complexity; Regions; Binding; Fus; Transportin
Sprache
Veröffentlichungsjahr
2016
HGF-Berichtsjahr
2016
ISSN (print) / ISBN
1433-7851
e-ISSN
1521-3773
Zeitschrift
Angewandte Chemie - Internationale Edition
Quellenangaben
Band: 55,
Heft: 47,
Seiten: 14847-14851
Verlag
Wiley
Verlagsort
Weinheim
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Structural Biology (STB)
POF Topic(s)
30505 - New Technologies for Biomedical Discoveries
30203 - Molecular Targets and Therapies
30203 - Molecular Targets and Therapies
Forschungsfeld(er)
Enabling and Novel Technologies
PSP-Element(e)
G-552800-001
G-503000-001
G-503000-001
PubMed ID
27763708
WOS ID
WOS:000388252700067
Scopus ID
84995562570
Erfassungsdatum
2016-10-24