Wang, M.; Yuan, M.; Vasilakos, A. V.; He, Y.; Ren, Z.

Protein language models (PLMs) like the ESM series encapsulate immense evolutionary knowledge within their high-dimensional continuous embeddings. However, these latent representations are densely entangled, obscuring the fine-grained biophysical constraints necessary for precise functional resolution. To unlock the full expressive power of these embeddings, we propose PLM-SAE, a mechanistic framework that employs Sparse Autoencoders (SAEs) to disentangle PLM representations into discrete, biologically interpretable activations. By isolating and directly intervening on critical functional features, we fundamentally enhance the structural and mutational awareness of the underlying embeddings. We rigorously validate this embedding enhancement on variant effect prediction (VEP). In the unsupervised zero-shot setting, our sparse modulation elevates the state-of-the-art ESM-3 model, yielding performance improvements across 114 deep mutational scanning datasets and delivering an 80.8% relative improvement on challenging targets like the human E3 ubiquitin ligase HECD1. Furthermore, our target-specific differentiable gating mechanism achieves consistent performance gains in over 80% of evaluated datasets with an average Spearman rho increase of +0.138. Finally, extending this approach to a cross-fitness multi-task architecture establishes new state-of-the-art results on 17 VenusMutHub datasets, highlighted by a 169.0% performance surge in small-molecule binding predictions. Our work demonstrates that refining the highly entangled latent manifold via sparse modulation provides a robust and generalizable foundation for enhancing downstream PLM capabilities.