Direct visualization of Ras proteins in spatially distinct cell surface microdomains

TLDR

Localization of signaling complexes to specific microdomains coordinates signal transduction at the plasma membrane. Using immunogold electron microscopy of plasma membrane sheets coupled with spatial point pattern analysis, we visualized morphologically featureless microdomains, including lipid rafts, in situ at high resolution. We observed that inner‑plasma‑membrane lipid rafts cluster cholesterol‑dependent 44‑nm microdomains covering 35 % of the surface, while inactive H‑ras localizes to both rafts and cholesterol‑independent domains, whereas activated H‑ras and K‑ras occupy distinct, nonraft, cholesterol‑independent microdomains stabilized by Galectin‑1 and farnesylation, respectively, illustrating a complex mosaic that likely underlies their divergent signaling outputs.

Abstract

Localization of signaling complexes to specific microdomains coordinates signal transduction at the plasma membrane. Using immunogold electron microscopy of plasma membrane sheets coupled with spatial point pattern analysis, we have visualized morphologically featureless microdomains, including lipid rafts, in situ and at high resolution. We find that an inner-plasma membrane lipid raft marker displays cholesterol-dependent clustering in microdomains with a mean diameter of 44 nm that occupy 35% of the cell surface. Cross-linking an outer-leaflet raft protein results in the redistribution of inner leaflet rafts, but they retain their modular structure. Analysis of Ras microlocalization shows that inactive H-ras is distributed between lipid rafts and a cholesterol-independent microdomain. Conversely, activated H-ras and K-ras reside predominantly in nonoverlapping, cholesterol-independent microdomains. Galectin-1 stabilizes the association of activated H-ras with these nonraft microdomains, whereas K-ras clustering is supported by farnesylation, but not geranylgeranylation. These results illustrate that the inner plasma membrane comprises a complex mosaic of discrete microdomains. Differential spatial localization within this framework can likely account for the distinct signal outputs from the highly homologous Ras proteins.