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Molecular insights on CALX-CBD12 interdomain dynamics from MD simulations, RDCs, and SAXS

Authors :
Layara A. Abiko
Phelipe Augusto Mariano Vitale
Michael Sattler
Martin Zacharias
Roberto Kopke Salinas
Cristiano L. P. Oliveira
Maximilia F. S. Degenhardt
Source :
Biophys J
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Na(+)/Ca(2+) exchangers (NCXs) are secondary active transporters that couple the translocation of Na(+) with the transport of Ca(2+) in the opposite direction. The exchanger is an essential Ca(2+) extrusion mechanism in excitable cells. It consists of a transmembrane domain and a large intracellular loop that contains two Ca(2+)-binding domains, CBD1 and CBD2. The two CBDs are adjacent to each other and form a two-domain Ca(2+) sensor called CBD12. Binding of intracellular Ca(2+) to CBD12 activates the NCX but inhibits the NCX of Drosophila, CALX. NMR spectroscopy and SAXS studies showed that CALX and NCX CBD12 constructs display significant interdomain flexibility in the apo state but assume rigid interdomain arrangements in the Ca(2+)-bound state. However, detailed structure information on CBD12 in the apo state is missing. Structural characterization of proteins formed by two or more domains connected by flexible linkers is notoriously challenging and requires the combination of orthogonal information from multiple sources. As an attempt to characterize the conformational ensemble of CALX-CBD12 in the apo state, we applied molecular dynamics (MD) simulations, NMR ((1)H-(15)N residual dipolar couplings), and small-angle x-ray scattering (SAXS) data in a combined strategy to select an ensemble of conformations in agreement with the experimental data. This joint approach demonstrated that CALX-CBD12 preferentially samples closed conformations, whereas the wide-open interdomain arrangement characteristic of the Ca(2+)-bound state is less frequently sampled. These results are consistent with the view that Ca(2+) binding shifts the CBD12 conformational ensemble toward extended conformers, which could be a key step in the NCXs’ allosteric regulation mechanism. This strategy, combining MD with NMR and SAXS, provides a powerful approach to select ensembles of conformations that could be applied to other flexible multidomain systems.

Details

ISSN :
00063495
Volume :
120
Database :
OpenAIRE
Journal :
Biophysical Journal
Accession number :
edsair.doi.dedup.....80acd19d340fbdbfbb7ef7cef62a9664