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This article introduces SimpleDesign, a novel generative model that bypasses traditional multi-stage training to directly optimize protein sequence and structure co-design in data space. By utilizing a Mixture-of-Transformer architecture, it effectively handles the distinct modalities of amino acid sequences and 3D structures while maintaining global attention across both. The approach demonstrates strong performance on benchmarks for unconditional generation and co-design tasks, offering a streamlined pathway for advancing protein engineering and drug discovery through advanced machine learning techniques.
SimpleDesign: A Joint Model for Protein Sequence and Structure Codesign
arXiv:2609.03377v1 Announce Type: new Abstract: Proteins are fundamental to biological processes, with their function determined by the complex interplay between the amino acid sequence and the three-dimensional structure. Developing generative models capable of understanding this intrinsically multi-modal relationship is crucial for fields like drug discovery and protein engineering. Existing models often rely on a multi-stage training process where autoencoders that tokenize data into latent representations are trained in a first stage. Secondly, a generative model is trained on the latent representation of the autoencoder(s), i.e., generative modeling in a latent space. We hypothesize that this multi-stage training is not necessary to obtain performant co-design models and thus present SimpleDesign, an effective multi-modal protein design model trained directly in the data space. SimpleDesign leverages a single-stage end-to-end objective that combines discrete cross-entropy for sequences and a regression objective for structures. In order to effectively model the difference in sequence and structure modalities, we develop a Mixture-of-Transformer architecture that allows modality-specific processing while keeping global self-attention over both modalities. We train SimpleDesign on over 2M sequence-structure pairs achieving strong performance across co-design and unconditional sequence/structure generation benchmarks.
Abstract:Proteins are fundamental to biological processes, with their function determined by the complex interplay between the amino acid sequence and the three-dimensional structure. Developing generative models capable of understanding this intrinsically multi-modal relationship is crucial for fields like drug discovery and protein engineering. Existing models often rely on a multi-stage training process where autoencoders that tokenize data into latent representations are trained in a first stage. Secondly, a generative model is trained on the latent representation of the autoencoder(s), i.e., generative modeling in a latent space. We hypothesize that this multi-stage training is not necessary to obtain performant co-design models and thus present SimpleDesign, an effective multi-modal protein design model trained directly in the data space. SimpleDesign leverages a single-stage end-to-end objective that combines discrete cross-entropy for sequences and a regression objective for structures. In order to effectively model the difference in sequence and structure modalities, we develop a Mixture-of-Transformer architecture that allows modality-specific processing while keeping global self-attention over both modalities. We train SimpleDesign on over 2M sequence-structure pairs achieving strong performance across co-design and unconditional sequence/structure generation benchmarks.
Published in Transactions on Machine Learning Research (TMLR), 2026. this https URL
Machine Learning (cs.LG); Biomolecules (q-bio.BM)
arXiv:2609.03377 [cs.LG]
(or arXiv:2609.03377v1 [cs.LG] for this version)
https://doi.org/10.48550/arXiv.2609.03377 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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Full text under the publisher's open licence · 288 words
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