Publication details

Insights into Stability and Folding of GNRA and UNCG Tetra loops Revealed by Microsecond Molecular Dynamics and Well-Tempered Metadynamics

Authors

HALDAR Susanta KUHROVÁ Petra BANÁŠ Pavel SPIWOK Vojtěch ŠPONER Jiří HOBZA Pavel OTYEPKA Michal

Year of publication 2015
Type Article in Periodical
Magazine / Source Journal of Chemical Theory and Computation
MU Faculty or unit

Central European Institute of Technology

Citation
web http://pubs.acs.org/doi/pdf/10.1021/acs.jctc.5b00010
Doi http://dx.doi.org/10.1021/acs.jctc.5b00010
Field Physical chemistry and theoretical chemistry
Keywords FREE-ENERGY LANDSCAPE; DI-GMP RIBOSWITCH; RNA HAIRPINS; DISTINCTIVE FEATURES; ANGSTROM RESOLUTION; HAMMERHEAD RIBOZYME; BACTERIAL RIBOSOME; REPLICA-EXCHANGE; SIMULATIONS; KINETICS
Description RNA hairpins capped by 5'-GNRA-3' or 5'-UNCG-3' tetraloops (TLs) are prominent RNA structural motifs. Despite their small size, a wealth of experimental data, and recent progress in theoretical simulations of their structural dynamics and folding, our understanding of the folding and unfolding processes of these small RNA elements is still limited. Theoretical description of the folding and unfolding processes requires robust sampling, which can be achieved by either an exhaustive time scale in standard molecular dynamics simulations or sophisticated enhanced sampling methods, using temperature acceleration or biasing potentials. Here, we study structural dynamics of 5'-GNRA-3' and 5'-UNCG-3' TLs by 15,us-long standard simulations and a series of well-tempered metadynamics, attempting to accelerate sampling by bias in a few chosen collective variables (CVs). Both methods provide useful insights. The unfolding and refolding mechanisms of the GNRA TL observed by well-tempered metadynamics agree with the (reverse) folding mechanism suggested by recent replica exchange molecular dynamics simulations. The orientation of the glycosidic bond of the G(L4) nudeobase is critical for the UUCG TL folding pathway, and our data strongly support the hypothesis that G(L4)-anti forms a kinetic trap along the folding pathway. Along with giving useful insight, our study also demonstrates that using only a few CVs apparently does not capture the full folding landscape of the RNA TLs. Despite using several sophisticated selections of the CVs, formation of the loop appears to remain a hidden variable, preventing a full convergence of the metadynamics. Finally, our data suggest that the unfolded state might be overstabilized by the force fields used.

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