Reconstitution of Contractile FtsZ Rings in Liposomes
Author(s) -
Masaki Osawa,
David E. Anderson,
Harold Erickson
Publication year - 2008
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1154520
Subject(s) - ftsz , cytoskeleton , tubulin , cell division , vesicle , microbiology and biotechnology , liposome , gtpase , biophysics , microtubule , biology , chemistry , cell , biochemistry , membrane
FtsZ is a tubulin homolog and the major cytoskeletal protein in bacterial cell division. It assembles into the Z ring, which contains FtsZ and a dozen other division proteins, and constricts to divide the cell. We have constructed a membrane-targeted FtsZ (FtsZ-mts) by splicing an amphipathic helix to its C terminus. When mixed with lipid vesicles, FtsZ-mts was incorporated into the interior of some tubular vesicles. There it formed multiple Z rings that could move laterally in both directions along the length of the liposome and coalesce into brighter Z rings. Brighter Z rings produced visible constrictions in the liposome, suggesting that FtsZ itself can assemble the Z ring and generate a force. No other proteins were needed for assembly and force generation.
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