Oxidative photocatalysis on membranes triggers non-canonical pyroptosis.
Chaiheon LeeMingyu ParkW C Bhashini WijesingheSeungjin NaChae Gyu LeeEunhye HwangGwangsu YoonJeong Kyeong LeeDeok-Ho RohYoon Hee KwonJihyeon YangSebastian A HughesJames E VinceJeong Kon SeoDuyoung MinTae-Hyuk KwonPublished in: Nature communications (2024)
Intracellular membranes composing organelles of eukaryotes include membrane proteins playing crucial roles in physiological functions. However, a comprehensive understanding of the cellular responses triggered by intracellular membrane-focused oxidative stress remains elusive. Herein, we report an amphiphilic photocatalyst localised in intracellular membranes to damage membrane proteins oxidatively, resulting in non-canonical pyroptosis. Our developed photocatalysis generates hydroxyl radicals and hydrogen peroxides via water oxidation, which is accelerated under hypoxia. Single-molecule magnetic tweezers reveal that photocatalysis-induced oxidation markedly destabilised membrane protein folding. In cell environment, label-free quantification reveals that oxidative damage occurs primarily in membrane proteins related to protein quality control, thereby aggravating mitochondrial and endoplasmic reticulum stress and inducing lytic cell death. Notably, the photocatalysis activates non-canonical inflammasome caspases, resulting in gasdermin D cleavage to its pore-forming fragment and subsequent pyroptosis. These findings suggest that the oxidation of intracellular membrane proteins triggers non-canonical pyroptosis.
Keyphrases
- visible light
- single molecule
- oxidative stress
- endoplasmic reticulum stress
- cell death
- nlrp inflammasome
- induced apoptosis
- label free
- quality control
- reactive oxygen species
- diabetic rats
- hydrogen peroxide
- single cell
- stem cells
- dna damage
- molecular dynamics simulations
- cell therapy
- ischemia reperfusion injury
- living cells
- nitric oxide
- high resolution
- mesenchymal stem cells
- small molecule
- mass spectrometry
- cell proliferation
- bone marrow
- molecularly imprinted
- heat shock
- fluorescent probe
- highly efficient