Abstract
The membrane protein NINJ1 mediates plasma membrane rupture in pyroptosis and other lytic cell death pathways. Here, we report the cryo-EM structure of a NINJ1 oligomer segmented from NINJ1 rings. Each NINJ1 subunit comprises amphipathic (⍺1, ⍺2) and transmembrane (TM) helices (⍺3, ⍺4) and forms a chain of subunits, mainly by the TM helices and ⍺1. ⍺3 and ⍺4 are kinked, and the Gly residues are important for function. The NINJ1 oligomer possesses a concave hydrophobic side that should face the membrane and a convex hydrophilic side formed by ⍺1 and ⍺2, presumably upon activation. This structural observation suggests that NINJ1 can form membrane disks, consistent with membrane fragmentation by recombinant NINJ1. Live-cell and super-resolution imaging uncover ring-like structures on the plasma membrane that are released into the culture supernatant. Released NINJ1 encircles a membrane inside, as shown by lipid staining. Therefore, NINJ1-mediated membrane disk formation is different from gasdermin-mediated pore formation, resulting in membrane loss and plasma membrane rupture.
Original language | English |
---|---|
Pages (from-to) | 2224-2235.e16 |
Journal | Cell |
Volume | 187 |
Issue number | 9 |
DOIs | |
State | Published - 25 Apr 2024 |
Externally published | Yes |
Keywords
- NINJ1
- NINJ2
- Ninjurin1
- Ninjurin2
- cryo-EM
- inflammasome
- inflammation
- lytic cell death
- plasma membrane rupture
- pyroptosis
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology