GyroNovo is a new framework for de novo peptide sequencing that improves fragment imputation by guiding the process with decoder errors observed during training. It introduces mass-aware attention using rotary embeddings to encode pairwise mass differences between spectral peaks, and creates easy and hard augmented views of spectra to train the decoder under varying corruption levels. Experiments on NovoBench demonstrate significant gains, with about 9 percentage points higher peptide-level precision and 7 percentage points higher amino-acid-level precision compared to the state-of-the-art baseline.
By Abdellah El Mekki, Laks V. S. Lakshmanan, Muhammad Abdul-Mageed
arXiv:2602. 22822v3 Announce Type: replace Abstract: Tandem mass spectrometry (MS/MS) is central to small molecule identification, but current deep learning systems for spectrum prediction still remain difficult to evaluate and deploy in practice.
By Yunhua Zhong, Yixuan Tang, Yifan Li, Pan Liu, Zhiwen Yang, Jie Yang, Jun Xia
arXiv:2607. 23607v1 Announce Type: new Abstract: Molecular structure elucidation from tandem mass spectra (MS/MS) is a central inverse problem in analytical chemistry.
By Xin Zhao, Yumin Liu, Zhuo Li, Weichu Zheng, Feng Zhu, Xiaokang Yang, Yaohui Jin, Yanyan Xu
arXiv:2608.30175v1 Announce Type: new
Abstract: Peptide-protein affinity models are often evaluated with a single data split, obscuring whether they interpolate among measurements for observed target...
By Jiaxin Tian, Darren An, Jun Li
MT-ProtBERT is a multi‑task extension of ProtBERT designed for classifying intrinsically disordered proteins (IDPs) in low‑data settings. It combines Dynamic Window Masking, a Multi‑Scale 1D Convolutional classifier, and auxiliary biochemistry‑informed objectives to jointly optimize masked language modeling and domain‑specific tasks. In experiments on phosphorylation site prediction and protein compaction prediction, MT‑ProtBERT outperforms the RNN‑based IDP model PARROT across all limited‑data tasks.
By Jian Sun, Kingshuk Ghosh, Lilianna Houston, Mohammad H. Mahoor
StabilityArc is a method that decodes protein sequence embeddings into generalizable stability landscapes. It uses a shared RoPE transformer to map frozen ESMC-600M residue representations into an Lx20 matrix of substitution effects, with a symmetric, contact-aware residual to predict epistasis. In extensive leave-one-protein-out tests on 134,794 ProteinGym variants, StabilityArc achieves a Spearman correlation of 0.7134, surpassing the best zero‑shot baseline, and further improves Kermut’s performance when used as a prior.
By Aaron L. Feller, Andrew D. Ellington, Claus O. Wilke