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体外偶联转录翻译:裂解液制备中的修饰对蛋白质组成和生物合成活性的影响。

In vitro coupled transcription translation: effects of modification in lysate preparation on protein composition and biosynthesis activity.

作者信息

Schindler P T, Baumann S, Reuss M, Siemann M

机构信息

Institut für Bioverfahrenstechnik, Universität Stuttgart, Germany.

出版信息

Electrophoresis. 2000 Jul;21(13):2606-9. doi: 10.1002/1522-2683(20000701)21:13<2606::AID-ELPS2606>3.0.CO;2-K.

Abstract

Cell-free extracts (lysates) from Escherichia coli were used for protein synthesis in vitro. Essential steps of the lysate preparation were modified and analyzed with respect to their impact on in vitro protein synthesis capacity, using the green fluorescent protein (GFP) as a target protein. Variably manufactured lysates of low, medium and higher protein synthesis activity, were examined by high resolution two-dimensional gel electrophoresis to determine whether the modifications result in substantial alterations in protein composition of the final lysate. The total number of proteins calculated from the gel maps did not vary for lysates with different activity and thus cannot serve as an evaluation parameter. Ribosomal proteins RP-S1, RP-L9, and RP-L10 were found in stoichiometric amounts for each of these lysates and in equal concentrations in comparison among the different lysates. Conversely, depending on the activity profiles, up to 7 different isoforms of the elongation factor EF-Ts were detected in the gel maps.

摘要

利用大肠杆菌的无细胞提取物(裂解物)进行体外蛋白质合成。以绿色荧光蛋白(GFP)作为靶蛋白,对裂解物制备的关键步骤进行了改进,并分析了其对体外蛋白质合成能力的影响。通过高分辨率二维凝胶电泳检测了具有低、中、高蛋白质合成活性的不同制备的裂解物,以确定这些改进是否会导致最终裂解物的蛋白质组成发生实质性变化。根据凝胶图谱计算出的不同活性裂解物的蛋白质总数没有变化,因此不能作为评估参数。在这些裂解物中均发现了化学计量的核糖体蛋白RP-S1、RP-L9和RP-L10,且不同裂解物之间的浓度相等。相反,根据活性谱,在凝胶图谱中检测到多达7种不同的延伸因子EF-Ts同工型。

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