Nanoscale manipulation of membrane curvature for probing endocytosis in live cells

Nanoscale plasma membrane curvature, generated in a controllable fashion by vertically aligned nanostructure arrays, promotes the accumulation of key endocytic proteins in live cells. Clathrin-mediated endocytosis (CME) involves nanoscale bending and inward budding of the plasma membrane, by which c...

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Veröffentlicht in:Nature nanotechnology 2017-08, Vol.12 (8), p.750-756
Hauptverfasser: Zhao, Wenting, Hanson, Lindsey, Lou, Hsin-Ya, Akamatsu, Matthew, Chowdary, Praveen D., Santoro, Francesca, Marks, Jessica R., Grassart, Alexandre, Drubin, David G., Cui, Yi, Cui, Bianxiao
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Sprache:eng
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Zusammenfassung:Nanoscale plasma membrane curvature, generated in a controllable fashion by vertically aligned nanostructure arrays, promotes the accumulation of key endocytic proteins in live cells. Clathrin-mediated endocytosis (CME) involves nanoscale bending and inward budding of the plasma membrane, by which cells regulate both the distribution of membrane proteins and the entry of extracellular species 1 , 2 . Extensive studies have shown that CME proteins actively modulate the plasma membrane curvature 1 , 3 , 4 . However, the reciprocal regulation of how the plasma membrane curvature affects the activities of endocytic proteins is much less explored, despite studies suggesting that membrane curvature itself can trigger biochemical reactions 5 , 6 , 7 , 8 . This gap in our understanding is largely due to technical challenges in precisely controlling the membrane curvature in live cells. In this work, we use patterned nanostructures to generate well-defined membrane curvatures ranging from +50 nm to −500 nm radius of curvature. We find that the positively curved membranes are CME hotspots, and that key CME proteins, clathrin and dynamin, show a strong preference towards positive membrane curvatures with a radius
ISSN:1748-3387
1748-3395
DOI:10.1038/nnano.2017.98