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Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system

BACKGROUND: Recently, some groups have reported on cell-free synthesis of functional membrane proteins (MPs) in the presence of exogenous liposomes (liposomes). Previously, we reported synthesis of a functional AtPPT1 plant phosphate transporter that was associated with liposomes during translation....

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Autores principales: Nozawa, Akira, Ogasawara, Tomio, Matsunaga, Satoko, Iwasaki, Takahiro, Sawasaki, Tatsuya, Endo, Yaeta
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090341/
https://www.ncbi.nlm.nih.gov/pubmed/21481249
http://dx.doi.org/10.1186/1472-6750-11-35
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author Nozawa, Akira
Ogasawara, Tomio
Matsunaga, Satoko
Iwasaki, Takahiro
Sawasaki, Tatsuya
Endo, Yaeta
author_facet Nozawa, Akira
Ogasawara, Tomio
Matsunaga, Satoko
Iwasaki, Takahiro
Sawasaki, Tatsuya
Endo, Yaeta
author_sort Nozawa, Akira
collection PubMed
description BACKGROUND: Recently, some groups have reported on cell-free synthesis of functional membrane proteins (MPs) in the presence of exogenous liposomes (liposomes). Previously, we reported synthesis of a functional AtPPT1 plant phosphate transporter that was associated with liposomes during translation. However, it is unclear whether or not lipid/MP complex formation is common to all types of MPs in the wheat cell-free system. RESULTS: AtPPT1 was synthesized using a wheat cell-free system with or without liposomes. AtPPT1 synthesized with liposomes showed high transport activity, but the activity of AtPPT1 synthesized without liposomes was less than 10% activity of that with liposomes. To test whether co-translational association with liposomes is observed in the synthesis of other MPs, we used 40 mammalian MPs having one to 14 transmembrane domains (TMDs) and five soluble proteins as a control. The association rate of all 40 MPs into liposomes was more than 40% (mean value: 59%), while that of the five soluble proteins was less than 20% (mean value: 12%). There were no significant differences in association rate among MPs regardless of the number of TMDs and synthesis yield. These results indicate that the wheat cell-free system is a highly productive method for lipid/MP complex formation and is suitable for large-scale preparation. The liposome association of green fluorescent protein (GFP)-fusion MPs were also tested and recovered as lipid/MP complex after floatation by Accudenz density gradient ultracentrifugation (DGU). Employment of GFP-MPs revealed optimal condition for Accudenz floatation. Using the optimized Accudenz DGU condition, P2RX4/lipid complexes were partially purified and detected as a major band by Coomassie Brilliant Blue (CBB)-staining after SDS-PAGE. CONCLUSION: Formation of lipid/AtPPT1 complex during the cell-free synthesis reaction is critical for synthesis of a functional MP. The lipid/MP complex during the translation was observed in all 40 MPs tested. At least 29 MPs, as judged by their higher productivity compared to GFP, might be suitable for a large-scale preparation. MPs synthesized by this method form lipid/MP complexes, which could be readily partially purified by Accudenz DGU. Wheat cell-free protein synthesis in the presence of liposomes will be a useful method for preparation of variety type of MPs.
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spelling pubmed-30903412011-05-10 Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system Nozawa, Akira Ogasawara, Tomio Matsunaga, Satoko Iwasaki, Takahiro Sawasaki, Tatsuya Endo, Yaeta BMC Biotechnol Methodology Article BACKGROUND: Recently, some groups have reported on cell-free synthesis of functional membrane proteins (MPs) in the presence of exogenous liposomes (liposomes). Previously, we reported synthesis of a functional AtPPT1 plant phosphate transporter that was associated with liposomes during translation. However, it is unclear whether or not lipid/MP complex formation is common to all types of MPs in the wheat cell-free system. RESULTS: AtPPT1 was synthesized using a wheat cell-free system with or without liposomes. AtPPT1 synthesized with liposomes showed high transport activity, but the activity of AtPPT1 synthesized without liposomes was less than 10% activity of that with liposomes. To test whether co-translational association with liposomes is observed in the synthesis of other MPs, we used 40 mammalian MPs having one to 14 transmembrane domains (TMDs) and five soluble proteins as a control. The association rate of all 40 MPs into liposomes was more than 40% (mean value: 59%), while that of the five soluble proteins was less than 20% (mean value: 12%). There were no significant differences in association rate among MPs regardless of the number of TMDs and synthesis yield. These results indicate that the wheat cell-free system is a highly productive method for lipid/MP complex formation and is suitable for large-scale preparation. The liposome association of green fluorescent protein (GFP)-fusion MPs were also tested and recovered as lipid/MP complex after floatation by Accudenz density gradient ultracentrifugation (DGU). Employment of GFP-MPs revealed optimal condition for Accudenz floatation. Using the optimized Accudenz DGU condition, P2RX4/lipid complexes were partially purified and detected as a major band by Coomassie Brilliant Blue (CBB)-staining after SDS-PAGE. CONCLUSION: Formation of lipid/AtPPT1 complex during the cell-free synthesis reaction is critical for synthesis of a functional MP. The lipid/MP complex during the translation was observed in all 40 MPs tested. At least 29 MPs, as judged by their higher productivity compared to GFP, might be suitable for a large-scale preparation. MPs synthesized by this method form lipid/MP complexes, which could be readily partially purified by Accudenz DGU. Wheat cell-free protein synthesis in the presence of liposomes will be a useful method for preparation of variety type of MPs. BioMed Central 2011-04-11 /pmc/articles/PMC3090341/ /pubmed/21481249 http://dx.doi.org/10.1186/1472-6750-11-35 Text en Copyright ©2011 Nozawa et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Nozawa, Akira
Ogasawara, Tomio
Matsunaga, Satoko
Iwasaki, Takahiro
Sawasaki, Tatsuya
Endo, Yaeta
Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
title Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
title_full Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
title_fullStr Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
title_full_unstemmed Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
title_short Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
title_sort production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090341/
https://www.ncbi.nlm.nih.gov/pubmed/21481249
http://dx.doi.org/10.1186/1472-6750-11-35
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