Bayesian Approximation of RNA Folding Times

RNA is a dynamic biomolecule with its function largely determined by its folding into complex structures. During the folding process, an RNA traverses through a series of intermediate structural states, with each transition occurring at variable rates that collectively influence the time required to reach the functional form. Understanding these folding kinetics is vital for predicting RNA behavior and optimizing applications in synthetic biology and drug discovery. While in silico kinetic RNA folding simulators are often computationally intensive and time-consuming, accurate approximations of the folding times can already be very informative to assess the efficiency of the folding process. Here, we present KinPFN, a novel approach that leverages prior-data fitted networks to directly model the posterior predictive distribution of RNA folding times. Trained on synthetic data representing arbitrary prior folding times, KinPFN efficiently approximates the cumulative distribution function of RNA folding times in a single forward pass, given only a few initial folding time examples. Our method offers a modular extension to RNA kinetics algorithms, promising significant computational speed-ups orders of magnitude faster, while achieving comparable results.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-03-05
DOI
https://doi.org/10.5281/zenodo.15228716
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
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article

Bayesian Approximation of RNA Folding Times

Zenodo (CERN European Organization for Nuclear Research)
RNA and protein synthesis mechanisms
article

Bayesian Approximation of RNA Folding Times

article en

Abstract

RNA is a dynamic biomolecule with its function largely determined by its folding into complex structures. During the folding process, an RNA traverses through a series of intermediate structural states, with each transition occurring at variable rates that collectively influence the time required to reach the functional form. Understanding these folding kinetics is vital for predicting RNA behavior and optimizing applications in synthetic biology and drug discovery. While in silico kinetic RNA folding simulators are often computationally intensive and time-consuming, accurate approximations of the folding times can already be very informative to assess the efficiency of the folding process. Here, we present KinPFN, a novel approach that leverages prior-data fitted networks to directly model the posterior predictive distribution of RNA folding times. Trained on synthetic data representing arbitrary prior folding times, KinPFN efficiently approximates the cumulative distribution function of RNA folding times in a single forward pass, given only a few initial folding time examples. Our method offers a modular extension to RNA kinetics algorithms, promising significant computational speed-ups orders of magnitude faster, while achieving comparable results.

Zenodo (CERN European Organization for Nuclear Research)
University of Vienna (AT), University of Freiburg (DE), Health Forecasting (US), Institute for Forecasting of the Slovak Academy of Sciences (SK)
Openalex Percentile: Top 60%
RNA and protein synthesis mechanisms
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