Metabolic EngineeringSystems BiologyPeer-reviewed journal article
Inferring secretory and metabolic pathway activity from omic data with secCellFie
Helen O. MassoniD, Mojtaba Samoudi, Caressa M. Robinson, Chih-Chung Kuo, Linus WeißiD, Km Shams‐Ud‐DohaiD, Alex Rosa CamposiD, Vijay TejwaniiD, Hussain DahodwalaiD, P MénardiD, Bjørn Gunnar Rude VoldborgiD, Bradley Robasky, Susan T. SharfsteiniD, Nathan E. LewisiD
Abstract
Understanding protein secretion has considerable importance in the biotechnology industry and important implications in a broad range of normal and pathological conditions including development, immunology, and tissue function. While great progress has been made in studying individual proteins in the secretory pathway, measuring and quantifying mechanistic changes in the pathways activity remains challenging due to the complexity of the biomolecular systems involved. Systems biology has begun to address this issue with the development of algorithmic tools for analyzing biological pathways; however most of these tools remain accessible only to experts in systems biology with extensive computational experience. Here, we expand upon the user-friendly CellFie tool which quantifies metabolic activity from omic data to include secretory pathway functions, allowing any scientist to infer protein secretion capabilities from omic data. We demonstrate how the secretory expansion of CellFie (secCellFie) can be used to predict metabolic and secretory functions across diverse immune cells, hepatokine secretion in a cell model of NAFLD, and antibody production in Chinese Hamster Ovary cells.
- organism: human
- organism: mouse
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: cell-cell communication
- research focus: trajectory inference
- approach: statistical model
- Citations
- 8
- FWCI
- 0.71
- Field percentile
- top 35%
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