Nanoscale imaging of bacterial infections by sphingolipid expansion microscopy.
Ralph GötzTobias C KunzJulian FinkFranziska SolgerJan SchlegelJuergen SeibelVera Kozjak-PavlovicThomas RudelMarkus SauerPublished in: Nature communications (2020)
Expansion microscopy (ExM) enables super-resolution imaging of proteins and nucleic acids on conventional microscopes. However, imaging of details of the organization of lipid bilayers by light microscopy remains challenging. We introduce an unnatural short-chain azide- and amino-modified sphingolipid ceramide, which upon incorporation into membranes can be labeled by click chemistry and linked into hydrogels, followed by 4× to 10× expansion. Confocal and structured illumination microscopy (SIM) enable imaging of sphingolipids and their interactions with proteins in the plasma membrane and membrane of intracellular organelles with a spatial resolution of 10-20 nm. As our functionalized sphingolipids accumulate efficiently in pathogens, we use sphingolipid ExM to investigate bacterial infections of human HeLa229 cells by Neisseria gonorrhoeae, Chlamydia trachomatis and Simkania negevensis with a resolution so far only provided by electron microscopy. In particular, sphingolipid ExM allows us to visualize the inner and outer membrane of intracellular bacteria and determine their distance to 27.6 ± 7.7 nm.
Keyphrases
- high resolution
- single molecule
- optical coherence tomography
- high speed
- high throughput
- electron microscopy
- induced apoptosis
- label free
- drug delivery
- cell cycle arrest
- photodynamic therapy
- atomic force microscopy
- computed tomography
- fatty acid
- multidrug resistant
- reactive oxygen species
- cell death
- fluorescence imaging
- hyaluronic acid
- drug discovery
- single cell
- molecularly imprinted
- wound healing
- induced pluripotent stem cells
- pluripotent stem cells