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Goricanec, D. ; Stehle, R. ; Egloff, P.* ; Grigoriu, S.* ; Plückthun, A.* ; Wagner, G.* ; Hagn, F.

Conformational dynamics of a G-protein α subunit is tightly regulated by nucleotide binding.

Proc. Natl. Acad. Sci. U.S.A. 113, E3629-E3638 (2016)
Verlagsversion Anhang DOI PMC
Heterotrimeric G proteins play a pivotal role in the signal-transduction pathways initiated by G-protein-coupled receptor (GPCR) activation. Agonist-receptor binding causes GDP-to-GTP exchange and dissociation of the Gα subunit from the heterotrimeric G protein, leading to downstream signaling. Here, we studied the internal mobility of a G-protein α subunit in its apo and nucleotide-bound forms and characterized their dynamical features at multiple time scales using solution NMR, small-angle X-ray scattering, and molecular dynamics simulations. We find that binding of GTP analogs leads to a rigid and closed arrangement of the Gα subdomain, whereas the apo and GDP-bound forms are considerably more open and dynamic. Furthermore, we were able to detect two conformational states of the Gα Ras domain in slow exchange whose populations are regulated by binding to nucleotides and a GPCR. One of these conformational states, the open state, binds to the GPCR; the second conformation, the closed state, shows no interaction with the receptor. Binding to the GPCR stabilizes the open state. This study provides an in-depth analysis of the conformational landscape and the switching function of a G-protein α subunit and the influence of a GPCR in that landscape.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Gpcr ; Nmr ; Saxs ; Signaling ; Structure; Heterotrimeric G-protein; Phospholipid-bilayer Nanodiscs; Crystal-structure; Relaxation Dispersion; Molecular-dynamics; Directed Evolution; Escherichia-coli; Coupled Receptor; Nmr Data; Activation
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Zeitschrift Proceedings of the National Academy of Sciences of the United States of America
Quellenangaben Band: 113, Heft: 26, Seiten: E3629-E3638 Artikelnummer: , Supplement: ,
Verlag National Academy of Sciences
Verlagsort Washington
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Structural Biology (STB)