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首页> 外文期刊>Journal of speech, language, and hearing research: JSLHR >Proteomic profiling of rat thyroarytenoid muscle.
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Proteomic profiling of rat thyroarytenoid muscle.

机译:大鼠甲状腺类肌肉的蛋白质组学分析。

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PURPOSE: Proteomic methodologies offer promise in elucidating the systemwide cellular and molecular processes that characterize normal and diseased thyroarytenoid (TA) muscle. This study examined methodological issues central to the application of 2-dimensional sodium dodecyl sulfate polyacrylamide gel electrophoresis (2D SDS-PAGE) to the study of the TA muscle proteome using a rat model. METHOD: 2D SDS-PAGE was performed using 4 chemically skinned rat TA muscle samples. Gel images were analyzed and compared. Protein spot detection and matching were performed using computational image analysis algorithms only and computational image analysis followed by visual inspection and manual error correction. A synthetic master gel, constructed to control for uninteresting biological variation and technical artifact due to differences in protein loading and staining, was evaluated against its constituent gels. RESULTS: Manual error correction resulted in a consistent increase in the number of protein spots detected (between 5.8% and 40.9%) and matched (from 25.8% to 70.8%) across all gels. Sensitivity and specificity of the automatic (computational) spot detection procedure, evaluated against the manual correction procedure, were 74.1% and 97.9%, respectively. Evaluation of protein quantitation parameter values revealed statistically significant differences (p < .0001) in optical density, area, and volume for matched protein spots across gels. The synthetic master gel successfully compensated for these intergel differences. CONCLUSIONS: Valid and reliable proteomic data are dependant on well-controlled manageable variability and well-defined unmanageable variability. Manual correction of spot detection and matching errors and the use of a synthetic master gel appear to be useful strategies in addressing these issues. With these issues accounted for, 2D SDS-PAGE may be applied to quantitative experimental comparisons of normal and disease conditions affecting voice, speech, and swallowing function.
机译:目的:蛋白质组学方法学有望阐明全系统的细胞和分子过程,这些过程表征了正常和患病的甲状腺素(TA)肌肉。这项研究检查了方法学问题,这些问题对于将二维十二烷基硫酸钠聚丙烯酰胺凝胶电泳(2D SDS-PAGE)应用于使用大鼠模型的TA肌肉蛋白质组研究至关重要。方法:使用4种化学皮肤的大鼠TA肌肉样品进行2D SDS-PAGE。凝胶图像进行了分析和比较。仅使用计算图像分析算法进行蛋白质斑点检测和匹配,然后使用计算图像分析进行目测和手动错误校正。针对其组成凝胶评估了合成的主凝胶,该主凝胶被构建为控制由于蛋白质加载和染色差异而引起的无用的生物学变化和技术伪像。结果:手动错误校正导致在所有凝胶上检测到的蛋白质斑点数量持续增加(介于5.8%和40.9%之间)并匹配(从25.8%到70.8%)。与手动校正程序相比,自动(计算)点检测程序的灵敏度和特异性分别为74.1%和97.9%。蛋白质定量参数值的评估显示,凝胶上匹配的蛋白质斑点的光密度,面积和体积在统计学上有显着差异(p <.0001)。合成的主胶成功地弥补了这些胶间差异。结论:有效和可靠的蛋白质组学数据取决于良好控制的可管理变异性和明确定义的不可管理变异性。手动纠正​​斑点检测和匹配错误以及使用合成母胶似乎是解决这些问题的有用策略。考虑到这些问题后,二维SDS-PAGE可以用于正常实验和影响语音,语音和吞咽功能的疾病条件的定量实验比较。

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