溶解
蛋白质生物合成
生物化学
体外
凝胶电泳
大肠杆菌
无细胞蛋白质合成
生物合成
化学
分子生物学
绿色荧光蛋白
核糖体蛋白
起始因子
生物
翻译(生物学)
色谱法
信使核糖核酸
酶
核糖体
核糖核酸
基因
作者
Petra Theresia Schindler,Sandra Baumann,Matthias Reuß,Martin Siemann
标识
DOI:10.1002/1522-2683(20000701)21:13<2606::aid-elps2606>3.0.co;2-k
摘要
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.
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