CocoRNA is a cooperative multi-agent reinforcement learning framework that tackles RNA inverse design by breaking the problem into smaller sub‑problems solved collaboratively by multiple agents. A centralized critic provides global structural guidance during training, allowing the agents to jointly optimize their design strategies. Experiments on the Rfam dataset show that CocoRNA outperforms state‑of‑the‑art methods in both success rate and design speed, and additional tests on other biological sequence design tasks demonstrate its broad effectiveness.
arXiv:2610.20277v1 Announce Type: new Abstract: Designing RNA sequences that satisfy target tertiary-structure objectives is an important problem in RNA engineering, with broad applications in synthe...
arXiv:2609.36885v1 Announce Type: cross Abstract: RNA design aims to identify sequences that fold into specified secondary structures. Existing methods formulate the task as target-specific search or...
arXiv:2510.03811v2 Announce Type: replace Abstract: We develop an approach for the de novo synthesis of messenger RNA (mRNA) sequences encoding target proteins. This requires optimizing multiple biol...
MORAD is an online reinforcement learning framework that trains a single shared policy for backbone‑conditioned RNA diffusion models, enabling structure‑conditioned RNA inverse design across diverse target backbones. It integrates backbone‑conditioned group sampling, group‑relative reward normalization, and a forward‑process diffusion objective, jointly optimizing six measurements—including tertiary geometry, base pairing, ensemble behavior, and sequence composition—by mapping each to a bounded desirability score and combining them with a weighted geometric mean. Compared to a tertiary‑structure‑only reward, MORAD improves 10 of 11 evaluation metrics, achieving significant gains in GDT‑TS, pairing MCC, and normalized ensemble defect, and surpasses existing methods such as RiboDiffusion, gRNAde, and RDesign on tertiary structural accuracy, secondary‑structure pairing, and thermodynamic quality.
arXiv:2506. 07459v4 Announce Type: replace Abstract: Protein generative models have shown remarkable promise in protein design, yet their success rates remain constrained by reliance on curated sequence-structure datasets and by misalignment between supervised objectives and real design goals.
arXiv:2605.01513v2 Announce Type: replace Abstract: Designing therapeutic messenger RNA (mRNA) requires generating full-length transcripts that optimally balance intracellular stability and translati...
The paper introduces MCTH (Monte Carlo Tree Hallucination), an inference-only framework that performs all‑atom biomolecular sequence‑structure co‑design by treating pretrained folding and inverse‑folding models as black‑box operators. MCTH uses Monte Carlo Tree Search to allocate a fixed inference budget across competing design trajectories, incorporating model confidence, uncertainty, and cross‑expert consensus. Experiments across protein‑RNA, protein‑DNA, protein‑protein, and protein‑ligand design show that adaptive search outperforms simpler sampling strategies, and evaluations with AlphaFold3 and Chai‑1 demonstrate transferability beyond the search‑time oracle.
arXiv:2610.19123v1 Announce Type: new Abstract: Generating novel molecules with desired properties is a central challenge in drug discovery. Although foundational work focused on de novo generation,...
La‑Ribo is a generative framework that jointly designs RNA nucleotide sequences and their three‑dimensional structures using geometry‑latent flow matching. It preserves a sparse phosphate‑sugar‑base scaffold while encoding nucleotide identity and local conformation in residue‑wise latent variables, which a shared flow network generates before an RNA‑specific decoder reconstructs all heavy atoms. The authors also built a large, quality‑controlled corpus of 168,561 RNA structures—combining experimental data with predictions from three folding models—to expand supervision, and demonstrate that La‑Ribo outperforms baselines in designability and co‑designability across sampling budgets and refolding models, while also enabling scaffold‑conditioned inverse folding without extra training.
PGFS++ is a synthesis‑aware reinforcement learning framework that improves molecular properties such as drug‑likeness or binding affinity while ensuring the resulting molecules can be synthesized and remain structurally similar to the input. It builds on PGFS+ by using trainable embedding lookup tables for reaction templates and second reactants, a more effective scoring function, and a refined RL algorithm. The method addresses a reward‑hacking failure mode by treating each input molecule as the start of a forward‑synthesis trajectory, applying learned reaction templates with in‑stock building blocks, and producing diverse, high‑quality outputs with explicit synthesis routes.
arXiv:2606. 07562v1 Announce Type: cross Abstract: RNA design consists of discovering a nucleotide sequence that optimizes predefined criteria, such as secondary structure.
arXiv:2607. 19044v1 Announce Type: new Abstract: Leveraging large language models (LLMs) for molecular generation has shown remarkable potential in chemical and drug design.