The Endo-GeneScreen platform identifies drug-like probes that regulate endogenous protein levels within physiological contexts
Year: 2025
Type: article
Abstract: Traditional phenotypic drug discovery platforms have suffered from poor scalability and a lack of mechanistic understanding of newly discovered phenotypic probes. To address this, we created Endo- GeneScreen (EGS), a high-throughput enabled screening platform that identifies bioactive small molecules capable of regulating endogenous protein expression encoded by any preselected target gene within a biologically appropriate context. As a proof-of-concept, EGS successfully identified drug candidates that up-regulate endogenous expression of neuronal Syngap1, a gene that causes a neurodevelopmental disorder when haploinsufficient. For example, SR-1815, a previously unknown and undescribed kinase inhibitor, alleviated major cellular consequences of Syngap1 loss-of-function by restoring normal SynGAP protein levels and dampening neuronal hyperactivity within haploinsufficient neurons. Moreover, we demonstrate that EGS assays accelerate preclinical development of identified drug candidates and facilitate mode-of-action deconvolution studies. Thus, EGS identifies first-in-class bioactive small molecule probes that promote biological discovery and precision therapeutic development.
Source: Nature Communications
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $6,990
Awards: Integrated Acoustic Transfer System for HTS Library Management, G1869372820, BioRaptr Replacement Dispensers to Support High Throughput Screening, G3227156675, G3241052728, G3567069129, G3807249683, Preclinical development of a precision therapy for a monogenic mental health disorder, Integrated Platform for Discovery and Validation of Probes that Restore Protein Expression in Single-Gene Causes of Autism and Related Disorders, Tandem Multi-modal Plate Readers for a High Throughput Screening platform, HTS Drug Discovery Dispensers
OpenAlex ID: W4417154690
