aGPCR-HEK: A Stable High-Expression Inducible Mammalian Cell Expression System for Adhesion GPCR Structural Biology Applications

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Authors: David Mordechai Favara, Christopher G. Tate
Cited by: 0
References: 43

Abstract

ADGRL4 is an adhesion G protein-coupled receptor (aGPCR) implicated in multiple tumours. In our experience, conventional insect cell-based baculovirus expression systems have not yielded sufficient correctly folded ADGRL4 protein for purification and cryo-electron microscopy (cryo-EM) analysis. Here, we describe aGPCR-HEK, a six-week protocol that establishes stable tetracycline-inducible mammalian HEK293S GnTI- TetR cell lines expressing N-terminally HA- and GFP-tagged aGPCRs. The method comprises lentiviral production in Lenti-X 293T cells, transduction of target adherent HEK293S GnTI- TetR cells, flow cytometry enrichment of uninduced GFP-positive cells displaying leaky expression, adaptation to suspension culture, and large-scale tetracycline induction and harvesting of cells for downstream purification and cryo-EM. The system yields reproducible, milligram-scale quantities of folded aGPCR suitable for structural and biochemical studies. Key features • Establishes a stable, tetracycline-inducible HEK293S GnTI- TetR expression system in adherent or suspension cells for high-level expression of N-terminally HA- and GFP-tagged aGPCRs. • Uses lentiviral transduction for efficient aGPCR genomic integration and employs a tetracycline-repressor enabling high-level expression following tetracycline induction. • Uses flow cytometry enrichment of leaky GFP-positive cells to enhance inducibility and yield. • Provides suspension culture adaptation and large-scale tetracycline induction for structural biology-grade protein production suitable for purification and cryo-EM analysis.

Fields of Study & Subjects

Receptor Mechanisms and Signaling Viral Infectious Diseases and Gene Expression in Insects Virus-based gene therapy research

Publication details

Journal / source
BIO-PROTOCOL
Volume
16
Issue
1392
Pages
e5621–e5621
Publication date
1 January 2026
Language
EN