Research Appraisals
Evidence-based critical appraisals of the latest medical research, systematically evaluated using Oxford CEBM methodology.
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Journal of proteome research
AI-Based Digital Pathology-Enabled Spatial-Omics Data Analyses of the Human Kidney
Identification of tissue-region-specific changes in glycosylation is crucial for understanding the pathogenesis of kidney diseases, yet it remains a great challenge. We developed a workflow that combines matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) data with AI-based digital pathology annotations of kidney functional tissue units (FTUs) to profile N-glycan distributions within biopsy tissues. This approach can generate molecular-level data relevant to diverse pathological outcomes, thereby aiding in the elucidation of disease mechanisms. As a proof-of-concept, we demonstrate that this AI-based digital pathology approach to MALDI data segmentation enables the detection and differentiation of N-glycosylation within FTUs of healthy kidney tissue. We then elucidated differences in N-glycosylation between the diseased kidney tissue samples from patients with different diagnoses. Sialic acid N-glycans, which have been linked to various kidney diseases, displayed enrichment in the glomeruli and tubules of tissues from patients diagnosed with diabetic kidney disease (DKD), whereas they were enriched in the tubules and arteries from patients with acute kidney injury (AKI), in comparison to healthy tissue. Furthermore, we found that polylactosamine N-glycans were enriched only in the AKI samples, indicating their potential roles in tubular injury and inflammation. This workflow has the potential to bridge the gap between region-specific glycosylation and its implications on FTUs in diseases, paving the way for targeted molecular imaging studies in the kidney and other tissues.
7 June 2026
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Context-informed subgraph foundation models enable interpretable protein-function prediction
Protein-function prediction is crucial for elucidating molecular mechanisms driving biological processes and therapeutics development. Despite numerous computational tools demonstrating promising performance, they fall short when predicting rare, uncharacterized functions or indirect activities. Here, we present COSMOS, a context-aware Gene Ontology (GO) subgraph mining system for protein-function prediction. By leveraging inductive subgraph foundation models and an enriched knowledge graph of protein-GO relationships, COSMOS performs zero-shot, few-shot, and low-homology protein-function prediction. Built on 7,923,952 functional semantic relationships, COSMOS demonstrates robust capabilities to (1) generate state-of-the-art predictions for GO classes with sparse or no experimental annotations, (2) provide interpretable functional subgraphs for transparent rationale analysis, and (3) deliver complementary benefits when integrated with existing embedding-based prediction methods. We anticipate that COSMOS will serve as a complementary approach to conventional protein annotation methods and an interpretable tool for predicting protein functions within underexplored GO classes, thereby advancing genomics and therapeutic research.
18 Apr 2026
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