Ontology highlight
ABSTRACT:
SUBMITTER: Sato TK
PROVIDER: S-EPMC3661704 | biostudies-literature | 2013 Jun
REPOSITORIES: biostudies-literature
Sato Takehiro K TK Tweten Rodney K RK Johnson Arthur E AE
Nature chemical biology 20130407 6
Perfringolysin O (PFO), a bacterial cholesterol-dependent cytolysin, binds a mammalian cell membrane, oligomerizes into a circular prepore complex (PPC) and forms a 250-Å transmembrane β-barrel pore in the cell membrane. Each PFO monomer has two sets of three short α-helices that unfold and ultimately refold into two transmembrane β-hairpin (TMH) components of the membrane-embedded β-barrel. Interstrand disulfide-bond scanning revealed that β-strands in a fully assembled PFO β-barrel were strict ...[more]