Molecular dynamics in multidimensional space explains how mutations affect the association path of neomycin to a riboswitch

• Published in: Proceedings of the National Academy of Sciences - PNAS 2024-04, Vol.121 (15), p.e2317197121
• Main Authors: Chyży, Piotr, Kulik, Marta, Shinobu, Ai, Re, Suyong, Sugita, Yuji, Trylska, Joanna
• Format: Article
• Language: English
• Subjects: Binding sites; Biological Sciences; Conformation; Free energy; Gene expression; Ligands; Molecular Conformation; Molecular dynamics; Molecular Dynamics Simulation; Mutants; Mutation; Neomycin; Neomycin - metabolism; Neomycin - pharmacology; Nucleic Acid Conformation; Physical Sciences; Reporter gene; Ribonucleic acid; Riboswitch - genetics; Riboswitches; RNA; Yeasts
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.2317197121

Riboswitches are messenger RNA (mRNA) fragments binding specific small molecules to regulate gene expression. A synthetic N1 riboswitch, inserted into yeast mRNA controls the translation of a reporter gene in response to neomycin. However, its regulatory activity is sensitive to single-point RNA mutations, even those distant from the neomycin binding site. While the association paths of neomycin to N1 and its variants remain unknown, recent fluorescence kinetic experiments indicate a two-step process driven by conformational selection. This raises the question of which step is affected by mutations. To address this, we performed all-atom two-dimensional replica-exchange molecular dynamics simulations for N1 and U14C, U14C[Formula: see text], U15A, and A17G mutants, ensuring extensive conformational sampling of both RNA and neomycin. The obtained neomycin association and binding paths, along with multidimensional free-energy profiles, revealed a two-step binding mechanism, consisting of conformational selection and induced fit. Neomycin binds to a preformed N1 conformation upon identifying a stable upper stem and U-turn motif in the riboswitch hairpin. However, the positioning of neomycin in the binding site occurs at different RNA-neomycin distances for each mutant, which may explain their different regulatory activities. The subsequent induced fit arises from the interactions of the neomycin's N3 amino group with RNA, causing the G9 backbone to rearrange. In the A17G mutant, the critical C6-A17/G17 stacking forms at a closer RNA-neomycin distance compared to N1. These findings together with estimated binding free energies coincide with experiments and elucidate why the A17G mutation decreases and U15A enhances N1 activity in response to neomycin.