The Kink-Turn 7 Motif: An Additional Test for RNA Force Field Performance

The kink-turn is a recurrent RNA structural motif that induces a sharp bend (kink) in the A-form RNA helix. It is defined by key structural features, including consecutive sheared AG base pairs, an A-minor interaction, and multiple base-sugar interactions. An accurate representation of these densely packed noncanonical interactions by molecular dynamics simulations poses a significant challenge for contemporary force fields (FFs). Here, we present extended simulations of the ribosomal kink-turn 7 (Kt-7) from <i>H.m.</i>, the so-called "consensual" kink-turn, using a broad spectrum of pair-additive and polarizable RNA FFs. None of the tested FFs manage to flawlessly describe all of the structural features of the Kt-7 although several FFs provide rather acceptable results and should not cause problems in simulations of larger RNAs containing a kink-turn. On aggregate, the widely used OL3 (ff99bsc0χ<sub>OL3</sub>) and polarizable AMOEBA FFs achieve the best performance for this motif. Interestingly, some more recently parametrized FF variants struggle to describe the Kt-7's tertiary A-minor interaction - a ubiquitous tertiary contact in RNA. This raises some concerns about the broader applicability of these FFs and suggests that they may be overfitted to small model systems, such as RNA tetranucleotides. In some cases, irreversible unkinking of the entire kink-turn motif can also be observed. The kink-turn motif is highly sensitive to variations in RNA FFs, and we strongly recommend its inclusion in training and benchmarking data sets as an important regression test to improve the robustness and accuracy of RNA FF parametrization.

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Publication Details

Journal
Journal of Chemical Theory and Computation
Published
2025-12-08
DOI
https://doi.org/10.1021/acs.jctc.5c00776
Citations
2
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
1.61
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article

The Kink-Turn 7 Motif: An Additional Test for RNA Force Field Performance

Miroslav Krepl, Jiřı́ Šponer, Michal Otyepka, Vojtěch Mlýnský et al.
2 citations
Journal of Chemical Theory and Computation
RNA and protein synthesis mechanisms
1.61
article

The Kink-Turn 7 Motif: An Additional Test for RNA Force Field Performance

Miroslav Krepl, Jiřı́ Šponer, Michal Otyepka, Vojtěch Mlýnský, Pavel Banáš, Martin Pykal, Toon Lemmens
article en
2 citations

Abstract

The kink-turn is a recurrent RNA structural motif that induces a sharp bend (kink) in the A-form RNA helix. It is defined by key structural features, including consecutive sheared AG base pairs, an A-minor interaction, and multiple base-sugar interactions. An accurate representation of these densely packed noncanonical interactions by molecular dynamics simulations poses a significant challenge for contemporary force fields (FFs). Here, we present extended simulations of the ribosomal kink-turn 7 (Kt-7) from <i>H.m.</i>, the so-called "consensual" kink-turn, using a broad spectrum of pair-additive and polarizable RNA FFs. None of the tested FFs manage to flawlessly describe all of the structural features of the Kt-7 although several FFs provide rather acceptable results and should not cause problems in simulations of larger RNAs containing a kink-turn. On aggregate, the widely used OL3 (ff99bsc0χ<sub>OL3</sub>) and polarizable AMOEBA FFs achieve the best performance for this motif. Interestingly, some more recently parametrized FF variants struggle to describe the Kt-7's tertiary A-minor interaction - a ubiquitous tertiary contact in RNA. This raises some concerns about the broader applicability of these FFs and suggests that they may be overfitted to small model systems, such as RNA tetranucleotides. In some cases, irreversible unkinking of the entire kink-turn motif can also be observed. The kink-turn motif is highly sensitive to variations in RNA FFs, and we strongly recommend its inclusion in training and benchmarking data sets as an important regression test to improve the robustness and accuracy of RNA FF parametrization.

Journal of Chemical Theory and ComputationVol. 21(24)
VSB - Technical University of Ostrava (CZ), Masaryk University (CZ), Czech Academy of Sciences, Institute of Biophysics (CZ), Regional Centre of Advanced Technologies and Materials (CZ), Palacký University Olomouc (CZ)
Openalex Percentile: Top 14%
RNA and protein synthesis mechanisms
1.61
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