Sep 2026· Tsinghua Science and Technology· 0 citations
Protein Structure and Dynamics
TL;DR
A graph representation-based protein sequence generation method that incorporates new noise addition and feature extraction methods, as well as a designed encoder-decoder called MixInfo, which generates sequences faster than other methods, and generates sequences closely resemble natural proteins, indicating the model’s feasibility and potential value in practical applications.
Abstract
Current AlphaFold3-based protein structure prediction has reached remarkable levels, but sequences that can be applied in practice are mostly generated using physics-based methods. Here, we introduce a graph representation-based protein sequence generation method: MixInfoFold which incorporates new noise addition and feature extraction methods, as well as our designed encoder-decoder called MixInfo. The noise addition method adds Gaussian noise positively correlated with the sequence length at the end of the main-chain, which enhances the model’s ability to understand the dynamic changes in protein structure. The feature extraction method includes a new feature calculated by assessing the area and distance of the main-chain atoms. The MixInfo iteratively computes the relationships between edge and node features, enabling a deeper exploration of the implicit sequence information within protein structures. Compared to the best model, our model achieves an improvement of 0.80%, 0.89%, and 3.28%in sequence recovery rates on the CATH4.2, CATH4.3, and Modelfinal datasets, respectively. Additionally, our model generates sequences faster than other methods, and generates sequences closely resemble natural proteins, indicating the model’s feasibility and potential value in practical applications.
This work introduces a symmetric dual-path architecture that both leverages PLMs for pretrained sequence evolution knowledge and MPLMs for pretrained structural knowledge to iteratively guide protein sequence generation.
Han-Dong Wang, Jiaxin Qi, Baisheng Lai et al.· 0 citations
Protein mutation effect generation asks a model to describe the functional consequence of a point mutation in natural language. Existing protein-to-text systems typically encode mutation information into undifferentiated representations, overlooking the organization of mutation-induced evidence across structural and bi...
Liuzhenghao Lv, Yu-Yang Liu, Yu-Yang Gao et al.· 0 citations
This work introduces ZEST (Zoned Encoding of Sequence Traits), an evolution-informed vocabulary derived from conserved regions of multiple sequence alignments that demonstrates that evolution-informed tokenization can substitute for massive parameter scaling, opening a new direction for efficient, biologically-grounded...
Biswajit Banerjee, Claudia A. Carreno, Anton S. Petrov· 0 citations
This work uses a general-purpose "post-training" algorithm grounded in statistical physics that employs quantitative experimental rankings to directly produce a sampler for diverse, high fitness sequences with fewer data points than competing methods.
Sebastian Ibarraran, Shriram Chennakesavalu, Frank Hu et al.· Journal of Chemical Informat...· 0 citations
Multiple sequence alignment (MSA) is a foundational task in computational biology, underpinning protein structure prediction, evolutionary analysis, and domain annotation. Traditional MSA algorithms rely on pairwise amino acid substitution matrices derived from conserved protein families. While effective for aligning c...
The central challenge in de novo protein design is generating plausible, mutually compatible structures and sequences, such that each designed sequence folds into its intended structure and the structure accommodates that sequence. Compared to typical two-stage design methods, which decouple the modeling of the interde...
Yuan-Le Mo, Bo Qiang, Hai-Tao Lin et al.· 0 citations
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