Hannes Röst

Adamo Young, Bo Wang, Hannes Röst

Tandem mass spectra capture fragmentation patterns that provide key structural information about a molecule. Although mass spectrometry is applied in many areas, the vast majority of small molecules lack experimental reference spectra. For over seventy years, spectrum prediction has remained a key challenge in the field. Existing deep learning methods do not leverage global structure in the molecule, potentially resulting in difficulties when generalizing to new data. In this work we propose a new model, MassFormer, for accurately predicting tandem mass spectra. MassFormer uses a graph transformer architecture to model long-distance relationships between atoms in the molecule. The transformer module is initialized with parameters obtained through a chemical pre-training task, then fine-tuned on spectral data. MassFormer outperforms competing approaches for spectrum prediction on multiple datasets, and is able to recover prior knowledge about the effect of collision energy on the spectrum. By employing gradient-based attribution methods, we demonstrate that the model can identify relationships between fragment peaks. To further highlight MassFormer's utility, we show that it can match or exceed existing prediction-based methods on two spectrum identification tasks. We provide open-source implementations of our model and baseline approaches, with the goal of encouraging future research in this area.

Adamo Young, Fei Wang, David S Wishart et al.

Compound identification from tandem mass spectrometry (MS/MS) data is a critical step in the analysis of complex mixtures. Typical solutions for the MS/MS spectrum to compound (MS2C) problem involve comparing the unknown spectrum against a library of known spectrum-molecule pairs, an approach that is limited by incomplete library coverage. Compound to MS/MS spectrum (C2MS) models can improve retrieval rates by augmenting real libraries with predicted MS/MS spectra. Unfortunately, many existing C2MS models suffer from problems with mass accuracy, generalization, or interpretability. We develop a new probabilistic method for C2MS prediction, FraGNNet, that can efficiently and accurately simulate MS/MS spectra with high mass accuracy. Our approach formulates the C2MS problem as learning a distribution over molecule fragments. FraGNNet achieves state-of-the-art performance in terms of prediction error and surpasses existing C2MS models as a tool for retrieval-based MS2C.

Leon L. Xu, Hannes L. Röst

Liquid Chromatography coupled to Mass Spectrometry (LC-MS) based methods are commonly used for high-throughput, quantitative measurements of the proteome (i.e. the set of all proteins in a sample at a given time). Targeted LC-MS produces data in the form of a two-dimensional time series spectrum, with the mass to charge ratio of analytes (m/z) on one axis, and the retention time from the chromatography on the other. The elution of a peptide of interest produces highly specific patterns across multiple fragment ion traces (extracted ion chromatograms, or XICs). In this paper, we formulate this peak detection problem as a multivariate time series segmentation problem, and propose a novel approach based on the Transformer architecture. Here we augment Transformers, which are capable of capturing long distance dependencies with a global view, with Convolutional Neural Networks (CNNs), which can capture local context important to the task at hand, in the form of Transformers with Convolutional Self-Attention. We further train this model in a semisupervised manner by adapting state of the art semisupervised image classification techniques for multi-channel time series data. Experiments on a representative LC-MS dataset are benchmarked using manual annotations to showcase the encouraging performance of our method; it outperforms baseline neural network architectures and is competitive against the current state of the art in automated peak detection.