Contributions and competition of Mg²⁺and K⁺in folding and stabilization of the Twister Ribozyme

Abstract

Native folded and compact intermediate states of RNA typically involve tertiary structuresin the presence of divalent ions such as Mg 2+ in a background of monovalent ions. In a recent study we showed how the presence of Mg 2+ impacts the transition from partially unfolded to folded states through a "push-pull" mechanism where the ion both favors and disfavors the sampling of specific phosphate-phosphate interactions. To better understand the ion atmosphere of RNA in folded and partially folded states results from atomistic Umbrella Sampling and oscillating chemical potential Grand Canonical Monte Carlo/Molecular Dynamics (GCMC/MD) simulations are used to obtain atomic-level details of the distributions of Mg 2+ and K + ions around Twister RNA. Results show the presence of 100 mM Mg 2+ to lead to increased charge neutralization over that predicted by counterion condensation theory. Upon going from partially unfolded to folded states overall charge neutralization increases at all studied ion concentrations that, while associated with an increase in the number of direct ion-phosphate interactions, is fully accounted for by the monovalent K + ions. Furthermore, K + preferentially interacts with purine N7 atoms of helical regions in partially unfolded states thereby potentially stabilizing them. Thus, both secondary helical structures and formation of tertiary structures leads to increased counterion condensation, thereby stabilizing those structural features of Twister. Notably, it is shown that K + can act as a surrogate for Mg 2+ by participating in specific interactions with non-sequential phosphate pairs that occur in the folded state, explaining the ability of Twister to self-cleave at sub-millimolar Mg 2+ concentrations. Kognole and MacKerell-3 -