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Biology subjects

Gerl, M.

Publications and source records attributed to Gerl, M..

2 recordsLinked to original sources

C-COMPASS: A Neural Network Tool for Multi-Omic Classification of Cell Compartments

Functional compartmentalization in eukaryotic cells is essential for maintaining physiological processes. The development of systematic organelle proteomic techniques, such as Protein Correlation Profiling (PCP) and Localization of Organelle Proteins by Isotope Tagging (LOPIT), has enhanced our understanding of organelle dynamics and protein localization. However, the complexity of the data and the need for advanced computational skills limit their accessibility. To address this, we introduce C-COMPASS, an open-source software featuring a user-friendly interface that utilizes a neural network-based regression model to predict the spatial distribution of proteins across cellular compartments. C-COMPASS manages complex multilocalization patterns and integrates protein abundance information to model organelle composition changes under various biological conditions. Using C-COMPASS, we mapped the organelle proteomic landscapes of humanized liver mice in different metabolic states and modeled changes in organelle composition to provide insights into cellular adaptations. Additionally, we extended cellular maps to the lipid level by co-generating protein and lipid profiles. C-COMPASS trains neural networks with marker protein profiles to predict lipid localizations, enabling parallel mapping of lipid and protein localization. This approach overcomes the lack of knowledge of organelle-specific lipid markers and identifies previously unknown organelle-specific lipid species. C-COMPASS offers a comprehensive solution for studying organelle dynamics at the multi-omics level, designed to be accessible without requiring extensive computational expertise or specialized high-performance computing equipment.

cell biology↗

LIPEA: Lipid Pathway Enrichment Analysis

MotivationAnalyzing associations among multiple omic variables to infer mechanisms that meaningfully link them is a crucial step in systems biology. Gene Set Enrichment Analysis (GSEA) was conceived to pursue this aim in computational genomics, unveiling significant pathways associated to certain gene signatures under investigation. Lipidomics is a rapidly growing omic field, and absolute quantification of lipid abundance by shotgun mass spectrometry is generating high-throughput datasets that depict lipid metabolism in a plethora of conditions and organisms. In addition, high-throughput lipidomics represents a new important ally to develop personalized medicine approaches, investigate the causes and predict effective biomarkers in metabolic diseases, and not only.\n\nResultsHere, we present Lipid Pathway Enrichment Analysis (LIPEA), a web-tool for over-representation analysis of lipid signatures and detection of the biological pathways in which they are enriched. LIPEA is a new valid resource for biologists and physicians to mine pathways significantly associated to a set of lipids, helping them to discover whether common and collective mechanisms are hidden behind those lipids. LIPEA was extensively tested and we provide two examples where our system gave successfully results related with Major Depression Disease (MDD) and insulin re-sistance.\n\nAvailabilityThe tool is available as web platform at https://lipea.biotec.tu-dresden.de.

bioinformatics↗