Evidence map›Paper›PMID 40662826›Full record

ArticleBioinformatics (Oxford, England)2025

EnsembleDesign: messenger RNA design minimizing ensemble free energy via probabilistic lattice parsing.

Ning Dai, Tianshuo Zhou, Wei Yu Tang, David H Mathews, Liang Huang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Gradient-based optimization for mRNA sequence design.Bioinformatics (Oxford, England) · 2026
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ning DaiSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97330, United States.ORCID 0009-0000-9925-7874
Tianshuo ZhouSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97330, United States.ORCID 0009-0008-4804-0825
Wei Yu TangSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97330, United States.ORCID 0009-0008-1141-9479
David H MathewsDepartment of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, NY 14642, United States.ORCID 0000-0002-2907-6557
Liang HuangSchool of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR 97330, United States.ORCID 0000-0001-6444-7045

Funding

NSF 2009071NSF 2330737
6 · The paper itself

Abstract

motivationThe task of designing optimized messenger RNA (mRNA) sequences has received much attention in recent years, thanks to breakthroughs in mRNA vaccines during the COVID-19 pandemic. Because most previous work aimed to minimize the minimum free energy (MFE) of the mRNA in order to improve stability and protein expression, which only considers one particular structure per mRNA sequence, millions of alternative conformations in equilibrium are neglected. More importantly, we prefer an mRNA to populate multiple stable structures and be flexible among them during translation when the ribosome unwinds it.

resultsTherefore, we consider a new objective to minimize the ensemble free energy of an mRNA, which includes all possible structures in its Boltzmann ensemble. However, this new problem is much harder to solve than the original MFE optimization. To address the increased complexity of this problem, we introduce EnsembleDesign, a novel algorithm that employs continuous relaxation to optimize the expected ensemble free energy over a distribution of candidate sequences. EnsembleDesign extends both the lattice representation of the design space and the dynamic programming algorithm from LinearDesign to their probabilistic counterparts. Our algorithm consistently outperforms LinearDesign in terms of ensemble free energy, especially on long sequences. Interestingly, as byproducts, our designs also enjoy lower average unpaired probabilities (which correlates with degradation) and flatter Boltzmann ensembles (more flexibility between conformations). AVAILABILITY AND IMPLEMENTATION: Our code is available on: https://github.com/LinearFold/EnsembleDesign.

Indexed as

RNA, MessengerAlgorithmsCOVID-19HumansNucleic Acid ConformationSARS-CoV-2SoftwareThermodynamicsRNA, Messenger

Identifiers

PMID40662826
PMCPMC12261492

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.