Good Papers

LEMON-ZEST: Evolution-Informed Tokenization for Efficient Protein Language Modeling

LEMON-ZEST uses evolution-informed tokenization to embed domain-level biological priors directly into protein language models. Its 200M-parameter LEMON model outperforms 600M to 3B parameter models on remote homology detection despite training on a single H100 GPU for one week. Evolution-informed to

Biswajit Banerjee, Claudia Alvarez Carreno, Anton S Petrov

Published 2026Atlanta Poster Session 6 · Fri, Dec 11, 4:30 PM–7:30 PM local time · Hall C1arXiv ↗OpenReview ↗

83%
OverallMust read
?
OverallMust readVote to see the scoreThe exact score shows once you've voted, so every vote is your own call. The first half of each home page shelf shows its scores.
Readers
–

Only vote on papers you've read. Sign in with GitHub to vote.

AI panel13/20reviewers recommend it
lenient 5/5
medium 7/10
strict 1/5
AI panel?Vote to see what the 20 AI reviewers said

Abstract

Protein Language Models (PLMs) have made remarkable progress following scaling laws established in natural language processing across sequence- and structure-based tasks, yet the potential of tokenization remains underexploited. Unlike human language, proteins preserve structure despite extensive sequence variation a property standard tokenization strategies fundamentally fail to capture. We introduce ZEST (Zoned Encoding of Sequence Traits), an evolution-informed vocabulary derived from conserved regions of multiple sequence alignments. ZEST allows embedding domain-level biological priors directly at the tokenization stage rather than learning them implicitly through scale. ZEST natively compresses sequences to an average token length of 4 residues, enabling our model to process 4,000 residues within a standard 1024-token context window. Building on this, we present LEMON (Layered Extraction of Molecular Ordering from Nature), a compact 200M-parameter sequence-based model for detection of remote homology between protein sequences trained on a single H100 GPU for one week. Despite its modest size, LEMON outperforms state-of-the-art models ranging from 600M to 3B parameters. Our results demonstrate that evolution-informed tokenization can substitute for massive parameter scaling, opening a new direction for efficient, biologically-grounded protein representation learning. All code, model weights, and results are publicly available under the MIT license.