π-SPECFormer: A Mass Spectrometry-based Foundation Model for Decoding the Dark Proteome

In mass-spectrometry–based proteomics, a substantial proportion of acquired spectra remain unidentified, concealing a vast reservoir of biological variations commonly termed the "dark proteome", potentially obscuring sequence mutations, non–canonical peptides and post–translational modifications. Existing deep-learning methods largely rely on supervised training with peptide–spectrum matches (PSMs), limiting their ability to learn from the much larger pool of unannotated spectra. Here we introduce π–SPECFormer, a mass–spectrometry foundation model pre-trained on 291 million spectra through a two-stage framework that combines self-supervised and PSMs–guided representation learning. π–SPECFormer transfers effectively to de novo peptide sequencing, spectrum clustering and modification detection, consistently outperforming task-specific baselines. When applied to proteomic profiles from 103 individuals with lung adenocarcinoma, the model identified nine high-confidence mutated peptides, including six that were absent from the reference databases. π–SPECFormer thus enables unbiased decoding of molecular complexity beyond the boundaries of the canonical proteome.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-09
DOI
https://doi.org/10.64898/2026.11.06.764812
Primary Topic
Advanced Proteomics Techniques and Applications
Type
preprint
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preprint

π-SPECFormer: A Mass Spectrometry-based Foundation Model for Decoding the Dark Proteome

Linhai Xie, Guibin Wang, Cheng Chang, Zhendong Liang et al.
bioRxiv (Cold Spring Harbor Laboratory)
Advanced Proteomics Techniques and Applications
preprint

π-SPECFormer: A Mass Spectrometry-based Foundation Model for Decoding the Dark Proteome

Linhai Xie, Guibin Wang, Cheng Chang, Zhendong Liang, Xiansong Huang, Yu Wang, Tianze Ling, Kaixuan Li, Jun Xia, Tingpeng Yang, Fuchu He, Yiming Zhang, Shaorong Chen, Rong Xu, Jun Zhu, Fan Xu, Stan Z. Li, Tao Liu
preprint en

Abstract

In mass-spectrometry–based proteomics, a substantial proportion of acquired spectra remain unidentified, concealing a vast reservoir of biological variations commonly termed the "dark proteome", potentially obscuring sequence mutations, non–canonical peptides and post–translational modifications. Existing deep-learning methods largely rely on supervised training with peptide–spectrum matches (PSMs), limiting their ability to learn from the much larger pool of unannotated spectra. Here we introduce π–SPECFormer, a mass–spectrometry foundation model pre-trained on 291 million spectra through a two-stage framework that combines self-supervised and PSMs–guided representation learning. π–SPECFormer transfers effectively to de novo peptide sequencing, spectrum clustering and modification detection, consistently outperforming task-specific baselines. When applied to proteomic profiles from 103 individuals with lung adenocarcinoma, the model identified nine high-confidence mutated peptides, including six that were absent from the reference databases. π–SPECFormer thus enables unbiased decoding of molecular complexity beyond the boundaries of the canonical proteome.

bioRxiv (Cold Spring Harbor Laboratory)
Westlake University (CN), Peng Cheng Laboratory (CN), Guangzhou Laboratory (CN), The Hong Kong University of Science and Technology (Guangzhou) (CN), Tsinghua University (CN)
Advanced Proteomics Techniques and Applications
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