Title of article :
Electron Cryomicroscopic Visualization of PomA/B Stator Units of the Sodium-driven Flagellar Motor in Liposomes
Author/Authors :
Koji Yonekura، نويسنده , , Toshiharu Yakushi، نويسنده , , Tatsuo Atsumi، نويسنده , , Saori Maki-Yonekura and Keiichi Namba، نويسنده , , Michio Homma، نويسنده , , Keiichi Namba، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
9
From page :
73
To page :
81
Abstract :
A motor protein complex of the bacterial flagellum, PomA/B from Vibrio alginolyticus, was reconstituted into liposomes and visualized by electron cryomicroscopy. PomA/B is a sodium channel, composed of two membrane proteins, PomA and PomB, and converts ion flux to the rotation of the flagellar motor. Escherichia coli and Salmonella have a homolog called MotA/B, which utilizes proton instead of sodium ion. PomB and MotB have a peptidoglycan-binding motif in their C-terminal region, and therefore PomA/B and MotA/B are regarded as the stator. Energy filtering electron cryomicroscopy enhanced the image contrast of the proteins reconstituted into liposomes and showed that two extramembrane domains with clearly different sizes stick out of the lipid bilayers on opposite sides. Image analysis combined with gold labeling and deletion of the peptidoglycan-binding motif revealed that the longer one, ∼70 Å long, is likely to correspond to the periplasmic domain, and the other, about half size, to the cytoplasmic domain.
Keywords :
bacterial flagellum , flagellar motor , stator , Liposome , energy filtering electron cryomicroscopy
Journal title :
Journal of Molecular Biology
Serial Year :
2006
Journal title :
Journal of Molecular Biology
Record number :
1247152
Link To Document :
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