TY - JOUR
T1 - Cell-free synthesis of cytochrome c oxidase, a multicomponent membrane protein
AU - Katayama, Yukie
AU - Shimokata, Kunitoshi
AU - Suematsu, Makoto
AU - Ogura, Takashi
AU - Tsukihara, Tomitake
AU - Yoshikawa, Shinya
AU - Shimada, Hideo
N1 - Funding Information:
Acknowledgements We thank for Dr. Yutaka Shimada for assistance with removing the high-frequency spectral components caused by interference from the visible/Soret absorption spectra. This work was supported in parts by the grants from MEXT and Keio University. M.S. is the Leader of Grant-in-Aid for Creative Scientific Research 17GS0429 and Global COE Program for Human Metabolomic Systems Biology from MEXT. T.T. is the Leader of Grant-in-Aid for Scientific Research on Priority Areas 16087026 for Functional Mechanism and Structural Organization of Biological Macromolecular Assemblies from MEXT. S.Y. is the Leader of Global COE Program for Picobiology: Life Science at the atomic level from MEXT.
PY - 2010/6
Y1 - 2010/6
N2 - Cell-free protein synthesis is a useful technique that can site-specifically incorporate isotope-labeled amino acids into proteins. This incorporation is essential for infrared analyses of the electronic state of a specific amino acid residue used to elucidate protein function. Although 17 membrane proteins have been synthesized in their active state by cell-free systems, to date no hetero-subunit protein has been synthesized with this technique, suggesting that there are serious technical limitations. Here we report the cell-free synthesis of Paracoccus denitrificans cytochrome c oxidase, a membrane protein complex composed of three distinct subunits that contain two heme A molecules and two redox-active copper centers. The synthesized protein exhibited normal Soret/vis absorption spectra and ferrocytochrome c oxidation activity.
AB - Cell-free protein synthesis is a useful technique that can site-specifically incorporate isotope-labeled amino acids into proteins. This incorporation is essential for infrared analyses of the electronic state of a specific amino acid residue used to elucidate protein function. Although 17 membrane proteins have been synthesized in their active state by cell-free systems, to date no hetero-subunit protein has been synthesized with this technique, suggesting that there are serious technical limitations. Here we report the cell-free synthesis of Paracoccus denitrificans cytochrome c oxidase, a membrane protein complex composed of three distinct subunits that contain two heme A molecules and two redox-active copper centers. The synthesized protein exhibited normal Soret/vis absorption spectra and ferrocytochrome c oxidation activity.
KW - E. coli cell-free system
KW - Heme A
KW - Paracoccus denitrificans
UR - http://www.scopus.com/inward/record.url?scp=77954425805&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77954425805&partnerID=8YFLogxK
U2 - 10.1007/s10863-010-9285-8
DO - 10.1007/s10863-010-9285-8
M3 - Article
C2 - 20373004
AN - SCOPUS:77954425805
SN - 0145-479X
VL - 42
SP - 235
EP - 240
JO - Journal of Bioenergetics and Biomembranes
JF - Journal of Bioenergetics and Biomembranes
IS - 3
ER -