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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >INTERLABORATORY REPRODUCIBILITY OF YEAST PROTEIN PATTERNS ANALYZED BY IMMOBILIZED PH GRADIENT TWO-DIMENSIONAL GEL ELECTROPHORESIS
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INTERLABORATORY REPRODUCIBILITY OF YEAST PROTEIN PATTERNS ANALYZED BY IMMOBILIZED PH GRADIENT TWO-DIMENSIONAL GEL ELECTROPHORESIS

机译:固定化PH梯度二维凝胶电泳分析酵母蛋白的实验室间可重复性

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An interlaboratory comparison was conducted on the positional and quantitative reproducibility of yeast proteins resolved by two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) using isoelectric focusing with immobilized pH gradient (pH 4-7) in the first dimension. The basic experimental setup was as follows: one laboratory prepared and distributed a [S-35]methionine-labeled total yeast protein extract (Goteborg, Sweden), another laboratory prepared the IPG strips to be used by all labs in this study (Munich, Germany), the third laboratory (Aarhus, Denmark) circulated the protocols and coordinated the modest attempts to unify them. Samples were run horizontally in the first dimension and vertically in the second. The gels were sent to Goteborg for processing by phosphoimager technology and computerized image analysis (PDQuest), and the 2-D PAGE resolved proteins were located and quantified automatically. A subset of 470 spots was manually matched in all gels out of an average of 1328 resolved proteins. The positional interlaboratory comparison revealed great pattern reproducibility, the correlation coefficient in no case being less than 0.9994. In absolute terms an average deviation of 2.8 mm (x-position) and 1.8 mm (y-position) were obtained for all nine gels (three gels per lab). The interlaboratory comparison of protein quantitation displayed higher variability, and the best correlation coefficient generated was 0.975. An average standard deviation of 34.5% was calculated for protein quantitation including all three labs, a value slightly higher than the intralaboratory variation (range 20-28%) Thus, despite differences in protocols, chemicals and equipment, the immobilized pH gradient technology gave extremely high positional and quantitative reproducibility. This will greatly facilitate the exchange of data and the establishment of multi-user image-based 2-D gel databases. [References: 26]
机译:实验室间比较是通过二维聚丙烯酰胺凝胶电泳(2-D PAGE)使用固定在第一个维度的固定pH梯度(pH 4-7)进行二维聚丙烯酰胺凝胶电泳(2-D PAGE)解析得到的酵母蛋白的位置和定量重现性。基本实验设置如下:一个实验室准备并分发了[S-35]蛋氨酸标记的总酵母蛋白提取物(瑞典哥德堡),另一实验室准备了IPG条带,供本研究中的所有实验室使用。德国),第三个实验室(丹麦奥尔胡斯)分发了协议,并协调了统一协议的适度尝试。样品在第一个维度上水平运行,在第二个维度上垂直运行。将凝胶发送到Goteborg,通过phosphoimager技术和计算机图像分析(PDQuest)进行处理,然后对2-D PAGE解析的蛋白质进行自动定位和定量。在所有凝胶中,平均1328个可分辨蛋白质中有470个斑点的子集被手动匹配。实验室间的位置比较显示出良好的图案可重复性,相关系数在任何情况下均不得小于0.9994。绝对而言,所有九种凝胶(每个实验室三种凝胶)的平均偏差为2.8 mm(x位置)和1.8 mm(y位置)。实验室间蛋白质定量比较显示出较高的变异性,产生的最佳相关系数为0.975。包括所有三个实验室在内的蛋白质定量计算的平均标准偏差为34.5%,该值略高于实验室内的变化(范围为2-28%)。因此,尽管协议,化学药品和设备有所不同,但固定的pH梯度技术仍可提供高位置和定量重现性。这将极大地促进数据交换和建立基于多用户图像的二维凝胶数据库。 [参考:26]

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