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Code for: Informing NMR experiments with molecular dynamics simulations to characterize the dominant open state of KcsA. https://doi.org/10.1101/2020.12.14.422800

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Informing NMR experiments with molecular dynamics simulations to characterize the dominant open state of KcsA


Sergio Pérez-Conesa,$^{1,a)}$ Eric G. Keeler,$^{2,a)}$ Dongyu Zhang,$^{2,a)}$ Lucie Delemotte,$^{2,a)}$ and Ann E. McDermott$^{2,b)}$

$^1$ KTH Royal Institute of Technology, Science for Life Laboratory, Stockholm,Sweden

$^2$ Department of Chemistry, Columbia University, New York, New York 10027,United States

$^{a)}$ These three authors contributed equally

$^{b)}$ Correspondance to: lucied@kth.se, aem5@columbia.edu

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This github repository contains the code and files for Informing NMR experiments with molecular dynamics simulations to characterize the dominant open state of KcsA which can be found as a article or preprint. Data files including inference models and MD trajectories can be found at https://osf.io/6h2z5/

Abstract

As the first potassium channel with a X-ray structure determined, and given its homology to eukaryotic channels, the pH-gated prokaryotic channel KcsA has been extensively studied. Nevertheless, questions related in particular to the allosteric coupling between its gates remain open. The many currently available X-ray crystallography structures appear to correspond to various stages of activation and inactivation, offering insights into the molecular basis of these mechanisms. Since these studies have required mutations, complexation with antibodies, and substitution of detergents for lipids, examining the channel under more native conditions is desirable. Solid-state NMR (SSNMR) can be used to study the wild-type protein under activating conditions (low pH), at room temperature, and in bacteriomimetic liposomes. In this work, we sought to structurally assign the activated state present in SSNMR experiments. We used a combination of molecular dynamics (MD) simulations, chemical shift prediction algorithms, and Bayesian inference techniques to determine which of the most plausible X-ray structures resolved to date best represents the activated state captured in SSNMR. We first identified specific nuclei with simulated NMR chemical shifts that differed significantly when comparing partially open vs. fully open ensembles from MD simulations. The simulated NMR chemical shifts for those specific nuclei were then compared to experimental ones, revealing that the simulation of the partially open state was in good agreement with the SSNMR data. Nuclei that discriminate effectively between partially and fully open states belong to residues spread over the sequence and provide a molecular level description of the conformational change.

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Code for: Informing NMR experiments with molecular dynamics simulations to characterize the dominant open state of KcsA. https://doi.org/10.1101/2020.12.14.422800

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