两个铜绿假单胞菌克隆的二维凝胶电泳图像分析

IF 0.1 Q4 MULTIDISCIPLINARY SCIENCES
Jose-Arturo Molina-Mora, Diana Chinchilla-Montero, Carolina Castro-Peña, F. García
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引用次数: 0

摘要

分析生物样品蛋白质含量的经典策略是二维凝胶电泳(2D-GE)。该技术通过等电点和分子量分离蛋白质,并拍摄图像用于后续分析。然而,由于凝胶容易变形,存在重叠的斑点和条纹,模糊和未染色的斑点等,对2D-GE图像的分析需要标准化的图像分析。这对最终用户(研究人员)来说是一个困难,他们需要免费和用户友好的解决方案。我们之前已经报道了2D-GE图像分析方案的标准化,在当前的研究中,我们将其应用于两种新的铜绿假单胞菌C25和C50。我们首先提取暴露于抗生素后的质周蛋白,然后进行2D-GE分析。使用我们的标准化方案对图像进行分析,预处理步骤后使用CellProfiler实现蛋白质斑点的识别。菌株之间的比较使用差异点分析,揭示了细菌之间蛋白质表达的特定模式。这些结果将有助于研究这些菌株在不同条件下的蛋白质组学分析的生物学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two-dimensional gel electrophoresis image analysis of two Pseudomonas aeruginosa clones
A classical strategy to analyse the protein content of a biological sample is the two-dimensional gel electrophoresis (2D-GE). This technique separates proteins by both isoelectric point and molecular weight, and images are taken for subsequent analyses. However, analyses of 2D-GE images require standardized image analysis due to susceptibility of gels to get deformed, presence of overlapping spots and stripes, fuzzy and unstained spots, and others. This represent a difficulty for final users (researchers), which demand for free and user-friendly solutions. We have previously reported the standardization of a protocol to analyse 2D-GE images, and in the current study we applied it to two new bacterial isolates Pseudomonas aeruginosa C25 and C50. We first extracted periplasmic proteins after exposure to antibiotics, and we then run a 2D-GE analysis. Images were analysed using our standardized protocol, achieving the identification of protein spots using CellProfiler after pre-processing step. Comparison between strains was done using differential spot analysis, revealing a specific pattern in the protein expression between bacteria. These results will help to study the biological meaning of these strains using proteomic profiling under different conditions.
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来源期刊
Tecnologia en Marcha
Tecnologia en Marcha MULTIDISCIPLINARY SCIENCES-
自引率
0.00%
发文量
93
审稿时长
28 weeks
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