bioRxivMolecular BiologyPreprint
FlexRibbon: Joint Sequence and Structure Pretraining for Protein Modeling
Jianwei ZhuiD, Yu ShiiD, Ran BiiD, Peiran Jin, Chang LiuiD, Zhenyu ZhangiD, Haitao HuangiD, Zekun Guo, Pipi HuiD, Fusong JuiD, Lin HuangiD, Xinwei Tai, Chenao LiiD, Kaiyuan GaoiD, Xinran Wei, Huanhuan XiaiD, Jia ZhangiD, Yaosen MiniD, Zun WangiD, Yusong WangiD, Liang HeiD, Haiguang LiuiD, Tao Qin
Abstract
AO_SCPLOWBSTRACTC_SCPLOWProtein foundation models have advanced rapidly, with most approaches falling into two dominant paradigms. Sequence-based language models (e.g., ESM-2) capture sequence semantics at scale, and a number of recent works incorporate structural signals into sequence encoders. MSA-based predictors (e.g., AlphaFold 2/3) achieve accurate folding by exploiting evolutionary couplings, but their reliance on homologous sequences makes them less reliable in highly mutated or alignment-sparse regimes. We present FlexRibbon{ddagger}, a pretrained protein model that jointly learns from amino acid sequences and three-dimensional structures. Our pretraining strategy combines masked language modeling with diffusion-based denoising, enabling bidirectional sequence-structure learning without requiring MSAs. Trained on both experimentally resolved structures and AlphaFold 2 predictions, FlexRibbon captures global folds as well as flexible conformations critical for biological function. Evaluated across diverse tasks spanning interface design, intermolecular interaction prediction, and protein function prediction, FlexRibbon establishes new state-of-the-art performance on 12 different tasks, with particularly strong gains in mutation-rich settings where MSA-based methods often struggle.
- assay: protein sequence
- assay: protein structure
- research focus: protein design
- research focus: protein structure prediction
- approach: deep learning
- approach: diffusion model
- Citations
- 0
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