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Boginski, V.

Publications and source records attributed to Boginski, V..

3 recordsLinked to original sources

DEEPNET-LLM: Highly accurate structure prediction of unknown metabolites from mass spectra via their molecular neighborhoods

Most molecular features detected by untargeted mass spectrometry-based metabolomics remain unannotated. This so-called 'dark matter' currently comprises more than 90% and likely holds uncharacterized bioactive chemistry. Structure prediction from fragmentation spectra remains an outstanding challenge, because a spectrum does not uniquely determine a structure and the space of candidate structures is mostly unbounded; correspondingly, existing methods rarely return the correct de novo structure as their top prediction. Here we describe De novo Ego network-Enabled Propagation and Neighborhood Extrapolation of Topology using Large Language Models (DEEPNET-LLM) reasoning approach, which uses Molecular Community Networking (MCN) to restrict the search of a query spectrum to its local neighborhood within the global metabolome, and applies AI reasoning to propagate structural information from neighbors to the query. For a collection of 900 authentic standards (2,249 spectra) that have never been publicly released to exclude possibility of data leakage, DEEPNET-LLM returned the correct structure as its top prediction for 84.7% of spectra. Accuracy was independent of precursor mass across a range over which the number of candidate structures grows by 30 orders of magnitude, and was comparable across ion polarity, adducts and in-source fragmentation. On a random subset of the public MassSpecGym benchmark, DEEPNET-LLM reached 85.9% top-1 accuracy excluding stereochemistry. We showcase the use of DEEPNET-LLM with an example of a discovery of tryptamine amidate of a bile acid in mouse gut, confirmed against a synthetic standard. The DEEPNET-LLM approach is orthogonal to existing in silico methods and can be combined with them.

bioinformatics↗

HNSW-MS: Hierarchical Graph Indexing Enables Accurate Real-Time Mass Spectral Similarity Search at Repository Scale

Spectral similarity comparison is the basis of mass spectrometry-based metabolomics, underpinning library matching, molecular network construction, and repository searches such as MASST. Public repositories now exceed billion spectra, and exhaustive pairwise comparison is increasingly limiting. We introduce HNSW-MS, which implements Hierarchical Navigable Small World graph indexing natively for mass spectra. It operates directly on GC-MS and LC-MS/MS spectra without embedding, so scores are identical to those of exhaustive comparison and results are fully reproducible. On the benchmark dataset of 8.4 million LC-MS/MS spectra, HNSW-MS is up to 900-fold faster than linear search, recall@1 and recall@10 achieve over 90%, with the recall-speedup tradeoff tunable at query. Such rapid retrieval allows for any query spectrum to be near-instantaneously integrated into a global molecular network. We demonstrate specific examples of use of global networking for molecular discovery, including uncovering a new pathway of stenothricin biosynthesis and a new dipeptide conjugate bile acid.

bioinformatics↗

Ordering molecular diversity in untargeted metabolomics via molecular community networking

Natures molecular diversity is not random but displays intricate organization stemming from biological necessity. Molecular networking connects metabolites with structural similarity, enabling molecular discoveries from mass spectrometry data using arbitrary similarity thresholds that can fracture natural metabolite families. We present molecular community networking (MCN), that optimizes connectivity for each metabolite, rescuing lost relationships and capturing otherwise "hidden" metabolite connections. Using MCN, we demonstrate the discovery of novel dipeptide-conjugated bile acids.

biochemistry↗