Morris Jeffrey S, Clark Brittan N, Gutstein Howard B
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd Unit 447, Houston, TX 77030-4009, USA.
Bioinformatics. 2008 Feb 15;24(4):529-36. doi: 10.1093/bioinformatics/btm590. Epub 2008 Jan 14.
One of the key limitations for proteomic studies using 2-dimensional gel electrophoresis (2DE) is the lack of rapid, robust and reproducible methods for detecting, matching and quantifying protein spots. The most commonly used approaches involve first detecting spots and drawing spot boundaries on individual gels, then matching spots across gels and finally quantifying each spot by calculating normalized spot volumes. This approach is time consuming, error-prone and frequently requires extensive manual editing, which can unintentionally introduce bias into the results.
We introduce a new method for spot detection and quantification called Pinnacle that is automatic, quick, sensitive and specific and yields spot quantifications that are reliable and precise. This method incorporates a spot definition that is based on simple, straightforward criteria rather than complex arbitrary definitions, and results in no missing data. Using dilution series for validation, we demonstrate Pinnacle outperformed two well-established 2DE analysis packages, proving to be more accurate and yielding smaller coefficiant of variations (CVs). More accurate quantifications may lead to increased power for detecting differentially expressed spots, an idea supported by the results of our group comparison experiment. Our fast, automatic analysis method makes it feasible to conduct very large 2DE-based proteomic studies that are adequately powered to find important protein expression differences.
Matlab code to implement Pinnacle is available from the authors upon request for non-commercial use.
使用二维凝胶电泳(2DE)进行蛋白质组学研究的关键限制之一是缺乏用于检测、匹配和定量蛋白质斑点的快速、可靠且可重复的方法。最常用的方法包括首先在单个凝胶上检测斑点并绘制斑点边界,然后在不同凝胶之间匹配斑点,最后通过计算标准化斑点体积来定量每个斑点。这种方法既耗时又容易出错,并且经常需要大量的人工编辑,这可能会无意中给结果引入偏差。
我们引入了一种名为Pinnacle的斑点检测和定量新方法,该方法具有自动、快速、灵敏和特异的特点,并且能产生可靠且精确的斑点定量结果。此方法采用了基于简单直接标准而非复杂任意定义的斑点定义,且不会产生缺失数据。通过使用稀释系列进行验证,我们证明Pinnacle优于两个成熟的2DE分析软件包,其结果更准确,变异系数(CVs)更小。更准确的定量可能会提高检测差异表达斑点的能力,我们的组间比较实验结果支持了这一观点。我们快速、自动的分析方法使得开展基于2DE的大规模蛋白质组学研究成为可能,这些研究有足够的能力发现重要的蛋白质表达差异。
如需非商业用途,可向作者索取实现Pinnacle的Matlab代码。