Secretome-Based Screening in Target Discovery.
Mei DingHanna TegelÅsa SivertssonSophia HoberArjan SnijderMats OrmöPer-Erik StrömstedtRick DaviesLovisa Holmberg SchiavonePublished in: SLAS discovery : advancing life sciences R & D (2020)
Secreted proteins and their cognate plasma membrane receptors regulate human physiology by transducing signals from the extracellular environment into cells resulting in different cellular phenotypes. Systematic use of secretome proteins in assays enables discovery of novel biology and signaling pathways. Several secretome-based phenotypic screening platforms have been described in the literature and shown to facilitate target identification in drug discovery. In this review, we summarize the current status of secretome-based screening. This includes annotation, production, quality control, and sample management of secretome libraries, as well as how secretome libraries have been applied to discover novel target biology using different disease-relevant cell-based assays. A workflow for secretome-based screening is shared based on the AstraZeneca experience. The secretome library offers several advantages compared with other libraries used for target discovery: (1) screening using a secretome library directly identifies the active protein and, in many cases, its cognate receptor, enabling a rapid understanding of the disease pathway and subsequent formation of target hypotheses for drug discovery; (2) the secretome library covers significant areas of biological signaling space, although the size of this library is small; (3) secretome proteins can be added directly to cells without additional manipulation. These factors make the secretome library ideal for testing in physiologically relevant cell types, and therefore it represents an attractive approach to phenotypic target discovery.
Keyphrases
- drug discovery
- high throughput
- small molecule
- induced apoptosis
- quality control
- gene expression
- current status
- stem cells
- signaling pathway
- cell proliferation
- endothelial cells
- mesenchymal stem cells
- epithelial mesenchymal transition
- bone marrow
- cell cycle arrest
- pi k akt
- electronic health record
- genome wide
- binding protein
- heat shock
- heat stress
- rna seq