Dutt M J, Lee K H
Department of Chemical Engineering, Cornell University, Ithaca, NY 14853-5201, USA.
Electrophoresis. 2001 May;22(9):1627-32. doi: 10.1002/1522-2683(200105)22:9<1627::AID-ELPS1627>3.0.CO;2-R.
A new variable for measuring the relative intensities of silver stained protein spots on two-dimensional gels is described. The scaled volume (SV) more accurately measures the intensity of protein spots and accounts for differences frequently encountered when trying to compare two gels than other variables such as relative volume ratio, optical density, or relative optical density. The SV scales the signal of interest by the noise (gel background) with secondary signals removed (spots not of interest, e.g., technical artifacts). The SV of spot intensities offers a better dynamic response to protein amount for the model proteins studied here. Depending on the quantity of protein loaded onto gels, we have observed a coefficient of variation range of 0.2 to 1.3. We also observe that the SV silver stain response follows a characteristic exponential profile for different proteins.
本文描述了一种用于测量二维凝胶上银染蛋白质斑点相对强度的新变量。与相对体积比、光密度或相对光密度等其他变量相比,缩放体积(SV)能更准确地测量蛋白质斑点的强度,并能解释在比较两张凝胶时经常遇到的差异。SV通过去除二次信号(非感兴趣的斑点,如技术假象)后的噪声(凝胶背景)对感兴趣的信号进行缩放。对于本文研究的模型蛋白质,斑点强度的SV对蛋白量具有更好的动态响应。根据加载到凝胶上的蛋白量,我们观察到变异系数范围为0.2至1.3。我们还观察到,不同蛋白质的SV银染响应呈现出特征性的指数分布。