Brauner Jan M, Groemer Teja W, Stroebel Armin, Grosse-Holz Simon, Oberstein Timo, Wiltfang Jens, Kornhuber Johannes, Maler Juan Manuel
Department of Psychiatry and Psychotherapy, Friedrich-Alexander-University of Erlangen-Nuremberg, Schwabachanlage 6, 091054 Erlangen, Germany.
BMC Bioinformatics. 2014 Jun 11;15:181. doi: 10.1186/1471-2105-15-181.
Various computer-based methods exist for the detection and quantification of protein spots in two dimensional gel electrophoresis images. Area-based methods are commonly used for spot quantification: an area is assigned to each spot and the sum of the pixel intensities in that area, the so-called volume, is used a measure for spot signal. Other methods use the optical density, i.e. the intensity of the most intense pixel of a spot, or calculate the volume from the parameters of a fitted function.
In this study we compare the performance of different spot quantification methods using synthetic and real data. We propose a ready-to-use algorithm for spot detection and quantification that uses fitting of two dimensional Gaussian function curves for the extraction of data from two dimensional gel electrophoresis (2-DE) images. The algorithm implements fitting using logical compounds and is computationally efficient. The applicability of the compound fitting algorithm was evaluated for various simulated data and compared with other quantification approaches. We provide evidence that even if an incorrect bell-shaped function is used, the fitting method is superior to other approaches, especially when spots overlap. Finally, we validated the method with experimental data of urea-based 2-DE of Aβ peptides andre-analyzed published data sets. Our methods showed higher precision and accuracy than other approaches when applied to exposure time series and standard gels.
Compound fitting as a quantification method for 2-DE spots shows several advantages over other approaches and could be combined with various spot detection methods.The algorithm was scripted in MATLAB (Mathworks) and is available as a supplemental file.
存在多种基于计算机的方法用于二维凝胶电泳图像中蛋白质斑点的检测和定量。基于面积的方法常用于斑点定量:为每个斑点分配一个区域,并将该区域内像素强度的总和(即所谓的体积)用作斑点信号的度量。其他方法使用光密度,即斑点中最强像素的强度,或者根据拟合函数的参数计算体积。
在本研究中,我们使用合成数据和真实数据比较了不同斑点定量方法的性能。我们提出了一种现成的斑点检测和定量算法,该算法使用二维高斯函数曲线拟合从二维凝胶电泳(2-DE)图像中提取数据。该算法使用逻辑复合进行拟合,计算效率高。对各种模拟数据评估了复合拟合算法的适用性,并与其他定量方法进行了比较。我们提供的证据表明,即使使用了不正确的钟形函数,拟合方法也优于其他方法,尤其是当斑点重叠时。最后,我们用基于尿素的Aβ肽二维凝胶电泳的实验数据验证了该方法,并重新分析了已发表的数据集。当应用于曝光时间序列和标准凝胶时,我们的方法比其他方法显示出更高的精度和准确性。
复合拟合作为二维凝胶电泳斑点的定量方法比其他方法具有几个优点,并且可以与各种斑点检测方法相结合。该算法用MATLAB(Mathworks)编写脚本,可作为补充文件获取。