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利用脂质体补充的小麦无细胞翻译系统生产和部分纯化膜蛋白。

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

机构信息

Cell-Free Science and Technology Research Center and the Venture Business, Laboratory, Ehime University, 3 Bunkyo-Cho, Matsuyama, Ehime 790-8577, Japan.

出版信息

BMC Biotechnol. 2011 Apr 11;11:35. doi: 10.1186/1472-6750-11-35.

Abstract

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.

摘要

背景

最近,一些研究小组报告了在含有外源性脂质体(liposomes)的情况下,无细胞合成功能性膜蛋白(MPs)的情况。之前,我们曾报道过在翻译过程中与脂质体相关的功能型 AtPPT1 植物磷酸盐转运蛋白的合成。然而,在小麦无细胞系统中,脂质/MP 复合物的形成是否普遍存在于所有类型的 MPs 中,尚不清楚。

结果

使用含有或不含有脂质体的小麦无细胞系统合成 AtPPT1。与脂质体共合成的 AtPPT1 表现出高转运活性,但不含脂质体共合成的 AtPPT1 的活性不到含脂质体共合成的 10%。为了测试脂质体共翻译关联是否存在于其他 MPs 的合成中,我们使用了 40 种具有一个至 14 个跨膜结构域(TMDs)和五种可溶性蛋白的哺乳动物 MPs 作为对照。所有 40 种 MPs 与脂质体的结合率均超过 40%(平均值:59%),而五种可溶性蛋白的结合率均低于 20%(平均值:12%)。无论 MPs 的 TMD 数量和合成产量如何,其结合率均无显著差异。这些结果表明,小麦无细胞系统是一种高效的形成脂质/MP 复合物的方法,适用于大规模制备。绿色荧光蛋白(GFP)融合 MPs 的脂质体结合也进行了测试,并在 Accudenz 密度梯度超速离心(DGU)浮选中作为脂质/MP 复合物回收。使用 GFP-MPs 显示出 Accudenz 浮选中的最佳条件。使用优化的 Accudenz DGU 条件,部分纯化了 P2RX4/脂质复合物,并在 SDS-PAGE 后通过考马斯亮蓝(CBB)染色检测到主要条带。

结论

在无细胞合成反应过程中形成脂质/AtPPT1 复合物对于功能性 MP 的合成至关重要。在所有测试的 40 种 MPs 中均观察到翻译过程中的脂质/MP 复合物。至少有 29 种 MPs,根据它们比 GFP 更高的生产力来判断,可能适合大规模制备。通过该方法合成的 MPs 形成脂质/MP 复合物,可通过 Accudenz DGU 进行部分纯化。在有脂质体存在的情况下进行小麦无细胞蛋白质合成将是制备多种类型 MPs 的有用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c1d/3090341/0519c36903fe/1472-6750-11-35-1.jpg

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