TY - JOUR
T1 - Cell-free synthesis of zinc-binding proteins
AU - Matsuda, Takayoshi
AU - Kigawa, Takanori
AU - Koshiba, Seizo
AU - Inoue, Makoto
AU - Aoki, Masaaki
AU - Yamasaki, Kazuhiko
AU - Seki, Motoaki
AU - Shinozaki, Kazuo
AU - Yokoyama, Shigeyuki
N1 - Funding Information:
Acknowledgements The authors thank Yukako Miyata, Emi Nunokawa, Yukiko Fujikura, Natsuko Matsuda, Natsumi Suzuki, Yasuko Tomo, Eiko Seki, Masaomi Ikari, and Fumiko Hiroyasu at RIKEN for technical assistance. The authors also thank Takashi Yabuki for valuable suggestions and comments. The authors are grateful to Azusa Ishii, Kiyomi Yajima, and Tomoko Nakayama for expert secretarial assistance. This work was supported by the RIKEN Structural Genomics/Proteomics Initiative (RSGI), the National Project on Protein Structural and Functional Analyses, Ministry of Education, Culture, Sports, Science, and Technology of Japan.
PY - 2006/6
Y1 - 2006/6
N2 - Cell-free protein synthesis has become one of the standard methods for protein expression. The cell-free method is suitable for the synthesis of a protein that requires a ligand for its enzymatic activity and/or structure formation and stabilization, since it is an open system, which allows us to add the proper ligand to the reaction mixture. A large number of proteins that require zinc for their function are involved in diverse cellular processes, including transcription, DNA replication, metabolism, and cell signaling. In this study, we analyzed the effects of zinc on the cell-free synthesis of plant-specific zinc-binding transcription factors. The solubility and/or stability of the proteins were significantly increased in the presence of the proper concentration of zinc during the cell-free reaction. NMR analyses confirmed that correctly folded proteins were synthesized by the cell-free method. These results indicate that the cell-free method can be used to synthesize correctly folded and functional zinc-binding proteins.
AB - Cell-free protein synthesis has become one of the standard methods for protein expression. The cell-free method is suitable for the synthesis of a protein that requires a ligand for its enzymatic activity and/or structure formation and stabilization, since it is an open system, which allows us to add the proper ligand to the reaction mixture. A large number of proteins that require zinc for their function are involved in diverse cellular processes, including transcription, DNA replication, metabolism, and cell signaling. In this study, we analyzed the effects of zinc on the cell-free synthesis of plant-specific zinc-binding transcription factors. The solubility and/or stability of the proteins were significantly increased in the presence of the proper concentration of zinc during the cell-free reaction. NMR analyses confirmed that correctly folded proteins were synthesized by the cell-free method. These results indicate that the cell-free method can be used to synthesize correctly folded and functional zinc-binding proteins.
KW - Arabido psis thaliana
KW - Cell-free protein synthesis
KW - In vitro translation
KW - Structural genomics
KW - Zinc-binding protein
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U2 - 10.1007/s10969-006-9012-1
DO - 10.1007/s10969-006-9012-1
M3 - Article
C2 - 17146616
AN - SCOPUS:33846164810
SN - 1345-711X
VL - 7
SP - 93
EP - 100
JO - Journal of Structural and Functional Genomics
JF - Journal of Structural and Functional Genomics
IS - 2
ER -