TMEM106B is a receptor mediating ACE2-independent SARS-CoV-2 cell entryMore about Open Access at the Crick
Authors listJim Baggen Maarten Jacquemyn Leentje Persoons Els Vanstreels Val Pye Antoni Wrobel Valeria Calvaresi Stephen R Martin Chloe Roustan Nora B Cronin Eamonn Reading Hendrik Jan Thibaut Thomas Vercruysse Piet Maes Frederik De Smet Angie Yee Toey Nivitchanyong Marina Roell Natalia Franco-Hernandez Herve Rhinn Alusha Andre Mamchak Maxime Ah Young-Chapon Eric Brown Peter Cherepanov Dirk Daelemans
SARS-CoV-2 is associated with broad tissue tropism, a characteristic often determined by the availability of entry receptors on host cells. Here, we show that TMEM106B, a lysosomal transmembrane protein, can serve as an alternative receptor for SARS-CoV-2 entry into angiotensin-converting enzyme 2 (ACE2)-negative cells. Spike substitution E484D increased TMEM106B binding, thereby enhancing TMEM106B-mediated entry. TMEM106B-specific monoclonal antibodies blocked SARS-CoV-2 infection, demonstrating a role of TMEM106B in viral entry. Using X-ray crystallography, cryogenic electron microscopy (cryo-EM), and hydrogen-deuterium exchange mass spectrometry (HDX-MS), we show that the luminal domain (LD) of TMEM106B engages the receptor-binding motif of SARS-CoV-2 spike. Finally, we show that TMEM106B promotes spike-mediated syncytium formation, suggesting a role of TMEM106B in viral fusion. Together, our findings identify an ACE2-independent SARS-CoV-2 infection mechanism that involves cooperative interactions with the receptors heparan sulfate and TMEM106B.
Issue number 16