Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system
<p>Abstract</p> <p>Background</p> <p>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...
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doaj-acad1cf1ae864b06b98d418d0ba05f972020-11-25T01:42:42ZengBMCBMC Biotechnology1472-67502011-04-011113510.1186/1472-6750-11-35Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation systemIwasaki TakahiroMatsunaga SatokoOgasawara TomioNozawa AkiraSawasaki TatsuyaEndo Yaeta<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>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.</p> http://www.biomedcentral.com/1472-6750/11/35 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Iwasaki Takahiro Matsunaga Satoko Ogasawara Tomio Nozawa Akira Sawasaki Tatsuya Endo Yaeta |
spellingShingle |
Iwasaki Takahiro Matsunaga Satoko Ogasawara Tomio Nozawa Akira Sawasaki Tatsuya Endo Yaeta Production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system BMC Biotechnology |
author_facet |
Iwasaki Takahiro Matsunaga Satoko Ogasawara Tomio Nozawa Akira Sawasaki Tatsuya Endo Yaeta |
author_sort |
Iwasaki Takahiro |
title |
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_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_sort |
production and partial purification of membrane proteins using a liposome-supplemented wheat cell-free translation system |
publisher |
BMC |
series |
BMC Biotechnology |
issn |
1472-6750 |
publishDate |
2011-04-01 |
description |
<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>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.</p> |
url |
http://www.biomedcentral.com/1472-6750/11/35 |
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