Analysis of Quantized and Efficiently Adapted Protein Language Models

Abstract:Background: Protein language models (PLMs) are increasingly used for sequence generation and property prediction, but their size makes fine-tuning and deployment expensive. The effects of quantization and parameter efficient fine-tuning on performance, representations and generation remain insufficiently characterized. Results: We evaluated 4-bit quantization and low-rank adapter fine-tuning (QLoRA) across ESM-2, ESMC, ProtBERT, ProtT5, Ankh, Ankh3 and Profluent-E1. Across protein prediction tasks, many model-task pairs retained more than 90% of full fine-tuning performance. Peak GPU memory savings approached 90% for the largest models, although performance and efficiency varied by model, dataset and training configuration. QLoRA often preserved early-layer representations while inducing task-specific adaptations in middle and late layers, resembling full fine-tuning with smaller representational changes. Training speed and power effects were more varied. For unconditional generation with ProLLaMA, ProtGPT2, ProGen2, ProteinGLM and ESM3, 4-bit quantization largely preserved predicted structural and sequence-level properties, but token-level analysis revealed model-dependent shifts in autoregressive output distributions. Conclusion: QLoRA and 4-bit quantization reduce PLM computational requirements, particularly GPU memory usage. Our results support QLoRA as a first-pass strategy for memory limited adaptation, reserving full fine-tuning for challenging tasks, unstable architectures or low validation recovery. For generative PLMs, sequence-level and structural metrics should be complemented with distributional analysis, since downstream predictions alone may miss quantization-induced shifts. These approaches can broaden access to large-scale protein modelling while requiring model- and task-specific validation.

Machine Learning (cs.LG); Quantitative Methods (q-bio.QM)

arXiv:2610.00665 [cs.LG]

(or arXiv:2610.00665v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2610.00665 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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