Transition Metal Binding Drives Folding of a Metalloregulatory Riboswitch by Modulating Conformational Flexibility at Helical Junctions

Abstract

Transition metal ions are crucial for bacterias survival. Bacteria employ metalloregulatory riboswitches to respond to varying metal ion concentrations. The czcD (NiCo) transcription riboswitch specifically senses Co2+, Ni2+, and Fe2+ ions at micromolar concentrations amid millimolar Mg2+. We used computer simulations with multi-resolution RNA models to understand how global conformational changes in the NiCo riboswitch are coupled to the remarkable specific binding of Co2+. We show that the riboswitch folds through an intermediate state, where a partially folded four-way junction (4WJ) creates an anionic pocket large enough to accommodate the binding of solvated divalent ions. The binding of Co2+ is coupled to the stability of the weak non-canonical G{middle dot}A base pairs at the helical junction that drive the formation of native-like coaxial stacking of four helices. The Co2+ binding further twists the 4WJ, which locks the ions in the bound state. Electronic structure calculations show that enhanced orbital interactions between conserved guanines in the 4WJ and Co2+ are responsible for the high specificity of the riboswitch in binding to Co2+ over Mg2+. We provide a framework for understanding and engineering tunable RNA-based biosensors and developing antimicrobials, as metal intoxication is an evolutionary strategy to inhibit bacterial growth.