Electron cryotomography of ESCRT assemblies and dividing <i>Sulfolobus</i> cells suggests that spiraling filaments are involved in membrane scission

Megan J. Dobro(Hampshire College), Rachel Y. Samson(Indiana University Bloomington), Zhiheng Yu(Howard Hughes Medical Institute), John McCullough(University of Utah), H. Ding(California Institute of Technology), Parkson Lee‐Gau Chong(Temple University), Stephen D. Bell(Indiana University Bloomington), Grant J. Jensen(California Institute of Technology)
Molecular Biology of the Cell
June 13, 2013
Cited by 105Open Access
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Abstract

The endosomal-sorting complex required for transport (ESCRT) is evolutionarily conserved from Archaea to eukaryotes. The complex drives membrane scission events in a range of processes, including cytokinesis in Metazoa and some Archaea. CdvA is the protein in Archaea that recruits ESCRT-III to the membrane. Using electron cryotomography (ECT), we find that CdvA polymerizes into helical filaments wrapped around liposomes. ESCRT-III proteins are responsible for the cinching of membranes and have been shown to assemble into helical tubes in vitro, but here we show that they also can form nested tubes and nested cones, which reveal surprisingly numerous and versatile contacts. To observe the ESCRT-CdvA complex in a physiological context, we used ECT to image the archaeon Sulfolobus acidocaldarius and observed a distinct protein belt at the leading edge of constriction furrows in dividing cells. The known dimensions of ESCRT-III proteins constrain their possible orientations within each of these structures and point to the involvement of spiraling filaments in membrane scission.


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