TY - JOUR
T1 - A conserved haem redox and trafficking pathway for cofactor attachment
AU - Richard-Fogal, Cynthia L.
AU - Frawley, Elaine R.
AU - Bonner, Eric R.
AU - Zhu, Huifen
AU - San Francisco, Brian
AU - Kranz, Robert G.
PY - 2009/8/19
Y1 - 2009/8/19
N2 - A pathway for cytochrome c maturation (Ccm) in bacteria, archaea and eukaryotes (mitochondria) requires the genes encoding eight membrane proteins (CcmABCDEFGH). The CcmABCDE proteins are proposed to traffic haem to the cytochrome c synthetase (CcmF/H) for covalent attachment to cytochrome c by unknown mechanisms. For the first time, we purify pathway complexes with trapped haem to elucidate the molecular mechanisms of haem binding, trafficking and redox control. We discovered an early step in trafficking that involves oxidation of haem (to Fe 3), yet the final attachment requires reduced haem (Fe 2). Surprisingly, CcmF is a cytochrome b with a haem never before realized, and in vitro, CcmF functions as a quinol:haem oxidoreductase. Thus, this ancient pathway has conserved and orchestrated mechanisms for trafficking, storing and reducing haem, which assure its use for cytochrome c synthesis even in limiting haem (iron) environments and reducing haem in oxidizing environments.
AB - A pathway for cytochrome c maturation (Ccm) in bacteria, archaea and eukaryotes (mitochondria) requires the genes encoding eight membrane proteins (CcmABCDEFGH). The CcmABCDE proteins are proposed to traffic haem to the cytochrome c synthetase (CcmF/H) for covalent attachment to cytochrome c by unknown mechanisms. For the first time, we purify pathway complexes with trapped haem to elucidate the molecular mechanisms of haem binding, trafficking and redox control. We discovered an early step in trafficking that involves oxidation of haem (to Fe 3), yet the final attachment requires reduced haem (Fe 2). Surprisingly, CcmF is a cytochrome b with a haem never before realized, and in vitro, CcmF functions as a quinol:haem oxidoreductase. Thus, this ancient pathway has conserved and orchestrated mechanisms for trafficking, storing and reducing haem, which assure its use for cytochrome c synthesis even in limiting haem (iron) environments and reducing haem in oxidizing environments.
KW - Cytochrome
KW - Haem
KW - Quinone
KW - Redox
UR - http://www.scopus.com/inward/record.url?scp=69249205419&partnerID=8YFLogxK
U2 - 10.1038/emboj.2009.189
DO - 10.1038/emboj.2009.189
M3 - Article
C2 - 19629033
AN - SCOPUS:69249205419
SN - 0261-4189
VL - 28
SP - 2349
EP - 2359
JO - EMBO Journal
JF - EMBO Journal
IS - 16
ER -