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This research addresses a critical failure mode in protein language models where strong guidance causes representations to collapse into random-like distributions that still satisfy optimization oracles. The authors propose a training-free post-hoc filtering method using Mahalanobis distance to retain only sequences that maintain natural activation statistics, thereby improving structural plausibility without modifying the generator. This work is essential for advancing reliable AI-driven protein design by ensuring generated candidates remain within the manifold of biologically viable structures.
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Off-Manifold Collapse in Guided Protein Language Models

arXiv3 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2608.18597v1 Announce Type: new Abstract: Protein language models are widely used priors for protein sequence design, and a growing body of work controls them at inference time as an alternative to fine-tuning. Such guidance faces a dilemma: mild enough to preserve natural activation statistics, it barely moves the property; strong enough to move it, the generations become progressively harder to fold. We show the failure has a specific and cheaply detectable signature, an off-manifold collapse of the model's own representations. Guided activations fall toward a region statistically indistinguishable from random amino-acid input, and the sequences degenerate to low complexity, yet the property oracle being optimized can still score these generations as a success. The optimized oracle can therefore fail to witness the collapse and, for solubility, can actively reward it, whereas structure and composition expose the failure. Because the failure is already visible in a finished candidate, we detect it at the output rather than modify the generator. We introduce a cheap density prior over natural protein activations and keep only the candidates that remain typical under it, a training-free post-hoc step we call Mahalanobis filtering. At matched guidance settings it improves both the property score and the structural plausibility of the sequences it keeps at negligible cost, without touching the generator, and transfers across different guidance methods. We release the activation statistic at https://huggingface.co/Shuibai12138/off-manifold-collapse-plm

Abstract:Protein language models are widely used priors for protein sequence design, and a growing body of work controls them at inference time as an alternative to fine-tuning. Such guidance faces a dilemma: mild enough to preserve natural activation statistics, it barely moves the property; strong enough to move it, the generations become progressively harder to fold. We show the failure has a specific and cheaply detectable signature, an off-manifold collapse of the model's own representations. Guided activations fall toward a region statistically indistinguishable from random amino-acid input, and the sequences degenerate to low complexity, yet the property oracle being optimized can still score these generations as a success. The optimized oracle can therefore fail to witness the collapse and, for solubility, can actively reward it, whereas structure and composition expose the failure. Because the failure is already visible in a finished candidate, we detect it at the output rather than modify the generator. We introduce a cheap density prior over natural protein activations and keep only the candidates that remain typical under it, a training-free post-hoc step we call Mahalanobis filtering. At matched guidance settings it improves both the property score and the structural plausibility of the sequences it keeps at negligible cost, without touching the generator, and transfers across different guidance methods. We release the activation statistic at this https URL

Machine Learning (cs.LG)

arXiv:2608.18597 [cs.LG]

(or arXiv:2608.18597v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2608.18597 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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