BeeRNA: tertiary structure-based RNA inverse folding using Artificial Bee Colony

Fuente: arXiv
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Autori principali: Mlaweh, Mehyar, Cazenave, Tristan, Alaya, Ines
Natura: Preprint
Pubblicazione: 2025
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author Mlaweh, Mehyar
Cazenave, Tristan
Alaya, Ines
author_facet Mlaweh, Mehyar
Cazenave, Tristan
Alaya, Ines
contents The Ribonucleic Acid (RNA) inverse folding problem, designing nucleotide sequences that fold into specific tertiary structures, is a fundamental computational biology problem with important applications in synthetic biology and bioengineering. The design of complex three-dimensional RNA architectures remains computationally demanding and mostly unresolved, as most existing approaches focus on secondary structures. In order to address tertiary RNA inverse folding, we present BeeRNA, a bio-inspired method that employs the Artificial Bee Colony (ABC) optimization algorithm. Our approach combines base-pair distance filtering with RMSD-based structural assessment using RhoFold for structure prediction, resulting in a two-stage fitness evaluation strategy. To guarantee biologically plausible sequences with balanced GC content, the algorithm takes thermodynamic constraints and adaptive mutation rates into consideration. In this work, we focus primarily on short and medium-length RNAs ($<$ 100 nucleotides), a biologically significant regime that includes microRNAs (miRNAs), aptamers, and ribozymes, where BeeRNA achieves high structural fidelity with practical CPU runtimes. The lightweight, training-free implementation will be publicly released for reproducibility, offering a promising bio-inspired approach for RNA design in therapeutics and biotechnology.
format Preprint
id arxiv_https___arxiv_org_abs_2511_21781
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle BeeRNA: tertiary structure-based RNA inverse folding using Artificial Bee Colony
Mlaweh, Mehyar
Cazenave, Tristan
Alaya, Ines
Biomolecules
Artificial Intelligence
The Ribonucleic Acid (RNA) inverse folding problem, designing nucleotide sequences that fold into specific tertiary structures, is a fundamental computational biology problem with important applications in synthetic biology and bioengineering. The design of complex three-dimensional RNA architectures remains computationally demanding and mostly unresolved, as most existing approaches focus on secondary structures. In order to address tertiary RNA inverse folding, we present BeeRNA, a bio-inspired method that employs the Artificial Bee Colony (ABC) optimization algorithm. Our approach combines base-pair distance filtering with RMSD-based structural assessment using RhoFold for structure prediction, resulting in a two-stage fitness evaluation strategy. To guarantee biologically plausible sequences with balanced GC content, the algorithm takes thermodynamic constraints and adaptive mutation rates into consideration. In this work, we focus primarily on short and medium-length RNAs ($<$ 100 nucleotides), a biologically significant regime that includes microRNAs (miRNAs), aptamers, and ribozymes, where BeeRNA achieves high structural fidelity with practical CPU runtimes. The lightweight, training-free implementation will be publicly released for reproducibility, offering a promising bio-inspired approach for RNA design in therapeutics and biotechnology.
title BeeRNA: tertiary structure-based RNA inverse folding using Artificial Bee Colony
topic Biomolecules
Artificial Intelligence
url https://arxiv.org/abs/2511.21781