mlsanityData to 7 Oct 2026

Bio2Token: All-atom tokenization of any biomolecular structure with Mamba

arXiv 2410.19110 ↗First posted 24 Oct 2024cs.LG cs.AIcited by 5

On the map: State-space sequence models (S4, Mamba) → Core SSM architectures for language

Abstract (arXiv)

Efficient encoding and representation of large 3D molecular structures with high fidelity is critical for biomolecular design applications. Despite this, many representation learning approaches restrict themselves to modeling smaller systems or use coarse-grained approximations of the systems, for example modeling proteins at the resolution of amino acid residues rather than at the level of individual atoms. To address this, we develop quantized auto-encoders that learn atom-level tokenizations of complete proteins, RNA and small molecule structures with reconstruction accuracies well below 1 Angstrom. We demonstrate that a simple Mamba state space model architecture is efficient compared to an SE(3)-invariant IPA architecture, reaches competitive accuracies and can scale to systems with almost 100,000 atoms. The learned structure tokens of bio2token may serve as the input for all-atom generative models in the future.

Key facts. Cited by 5 papers in the map (data through 7 Oct 2026). Placed in Core SSM architectures for language, one of 10 directions in State-space sequence models (S4, Mamba). Builds on 16 of its 36 references that are in the map. First posted on arXiv 24 Oct 2024.

Builds on

16 of 36 references.

Closest ancestors · 3

Same direction, newest first

  1. 2024Transformers are SSMs: Generalized Models and Efficient Algorithms Through Structured State Space Duality31 May
  2. 2023Mamba: Linear-Time Sequence Modeling with Selective State Spaces1 Dec
  3. 2021Efficiently Modeling Long Sequences with Structured State Spaces31 Oct

Other references · 13

  1. 2017Attention Is All You Needcited by 59,932
  2. 2014Adam: A Method for Stochastic Optimizationcited by 36,960
  3. 2017Neural Discrete Representation Learningcited by 4,650
  4. 2022Equivariant Diffusion for Molecule Generation in 3Dcited by 666
  5. 2023Finite Scalar Quantization: VQ-VAE Made Simplecited by 425
  6. 2022Structure-based Drug Design with Equivariant Diffusion Modelscited by 213
  7. 2023Language models can generate molecules, materials, and protein binding sites directly in three dimensions as XYZ, CIF, and PDB filescited by 59
  8. 2019A Purely Algebraic Justification of the Kabsch-Umeyama Algorithmcited by 24
  9. 2024FoldToken: Learning Protein Language via Vector Quantization and Beyondcited by 21
  10. 2024BindGPT: A Scalable Framework for 3D Molecular Design via Language Modeling and Reinforcement Learningcited by 12
  11. 2024Geometry Informed Tokenization of Molecules for Language Model Generationcited by 10
  12. 2024Learning the Language of Protein Structurecited by 9
1 more
  1. 2024nabla2DFT: A Universal Quantum Chemistry Dataset of Drug-Like Molecules and a Benchmark for Neural Network Potentialscited by 2

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Cited by year (2026 to 7 Oct)

Citing papers per year: 2025: 3; 2026: 2.

5 papers.

Similar, not cited

Close in wording, no citation either way

  1. 2026SinAE: A Single-Architecture Flow-Matching Autoencoder for Cross-Domain Atomic Systems
  2. 2025Unified all-atom molecule generation with neural fields
  3. 2025ProteinAE: Protein Diffusion Autoencoders for Structure Encoding
  4. 2026Scalable Peptide Design via Memory-Efficient Equivariant Transformer
  5. 2023Ophiuchus: Scalable Modeling of Protein Structures through Hierarchical Coarse-graining SO(3)-Equivariant Autoencoders
  6. 2022Protein Sequence and Structure Co-Design with Equivariant Translation
  7. 2025UniMoMo: Unified Generative Modeling of 3D Molecules for De Novo Binder Design
  8. 2026Minimal-Action Discrete Schr"odinger Bridge Matching for Peptide Sequence Design