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ProtLingo advances protein language modeling by integrating conditional local memory and sparse expert routing to reduce computational costs while maintaining high accuracy in mutation prediction. This framework demonstrates that efficient parameter activation via Mixture-of-Experts can effectively capture complex sequence-function relationships without relying on massive dense backbones. The approach offers a scalable path for applying AI to biological sequence analysis with improved resource efficiency.
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ProtLingo: Efficient Protein Language Modeling via Conditional Memory and Expert Routing

arXiv2 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2609.04793v1 Announce Type: new Abstract: Proteins perform diverse cellular functions, and even single amino-acid substitutions can alter stability, activity, or molecular interactions. Protein language models (PLMs) provide a scalable approach for modeling such sequence--function relationships from unlabeled sequences, but increasing the size of dense Transformer backbones often brings substantial computational cost without consistently improving mutation-sensitive prediction. We introduce ProtLingo, an efficient PLM framework that augments a pretrained single-sequence backbone with conditional local memory and sparse expert routing. ProtLingo maps contextual residue representations into route-specific discrete codes, composes centered local windows into latent $N$-gram addresses, and retrieves reusable residual signals associated with recurring local sequence contexts. In parallel, selected feed-forward blocks are upcycled into sparse Mixture-of-Experts layers with shared and routed experts, enabling residue-dependent computation while activating only a subset of parameters. Experiments on protein fitness prediction, FLIP benchmarks, and supervised contact prediction show that ProtLingo achieves competitive performance with a 150M-scale backbone, including strong parameter efficiency on mutation-effect prediction and preserved long-range structural representations.

Abstract:Proteins perform diverse cellular functions, and even single amino-acid substitutions can alter stability, activity, or molecular interactions. Protein language models (PLMs) provide a scalable approach for modeling such sequence--function relationships from unlabeled sequences, but increasing the size of dense Transformer backbones often brings substantial computational cost without consistently improving mutation-sensitive prediction. We introduce ProtLingo, an efficient PLM framework that augments a pretrained single-sequence backbone with conditional local memory and sparse expert routing. ProtLingo maps contextual residue representations into route-specific discrete codes, composes centered local windows into latent $N$-gram addresses, and retrieves reusable residual signals associated with recurring local sequence contexts. In parallel, selected feed-forward blocks are upcycled into sparse Mixture-of-Experts layers with shared and routed experts, enabling residue-dependent computation while activating only a subset of parameters. Experiments on protein fitness prediction, FLIP benchmarks, and supervised contact prediction show that ProtLingo achieves competitive performance with a 150M-scale backbone, including strong parameter efficiency on mutation-effect prediction and preserved long-range structural representations.

Artificial Intelligence (cs.AI)

arXiv:2609.04793 [cs.AI]

(or arXiv:2609.04793v1 [cs.AI] for this version)

https://doi.org/10.48550/arXiv.2609.04793 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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