Xun Zhiyin, Sowell Renã A, Kaufman Thomas C, Clemmer David E
Department of Chemistry, Indiana University, Bloomington, Indiana 47405-7102, USA.
Mol Cell Proteomics. 2008 Jul;7(7):1191-203. doi: 10.1074/mcp.M700467-MCP200. Epub 2008 Mar 18.
A global isotopic labeling strategy combined with multidimensional liquid chromatographies and tandem mass spectrometry was used for quantitative proteome analysis of a presymptomatic A53T alpha-synuclein Drosophila model of Parkinson disease (PD). Multiple internal standard proteins at different concentration ratios were spiked into samples from PD-like and control animals to assess quantification accuracy. Two biological replicates isotopically labeled in forward and reverse directions were analyzed. A total of 253 proteins were quantified with a minimum of two identified peptide sequences (for each protein); 180 ( approximately 71%) proteins were detected in both forward and reverse labeling measurements. Twenty-four proteins were differentially expressed in A53T alpha-synuclein Drosophila; up-regulation of troponin T and down-regulation of fat body protein 1 were confirmed by Western blot analysis. Elevated expressions of heat shock protein 70 cognate 3 and ATP synthase are known to be directly involved in A53T alpha-synuclein-mediated toxicity and PD; three up-regulated proteins (muscle LIM protein at 60A, manganese-superoxide dismutase, and troponin T) and two down-regulated proteins (chaoptin and retinal degeneration A) have literature-supported associations with cellular malfunctions. That these variations were observed in presymptomatic animals may shed light on the etiology of PD. Protein interaction network analysis indicated that seven proteins belong to a single network, which may provide insight into molecular pathways underlying PD. Gene Ontology analysis indicated that the dysregulated proteins are primarily associated with membrane, endoplasmic reticulum, actin cytoskeleton, mitochondria, and ribosome. These associations support prior findings in studies of the A30P alpha-synuclein Drosophila model (Xun, Z. Y., Sowell, R. A., Kaufman, T. C., and Clemmer, D. E. (2007) Protein expression in a Drosophila model of Parkinson's disease. J. Proteome Res. 6, 348-357; Xun, Z. Y., Sowell, R. A., Kaufman, T. C., and Clemmer, D. E. (2007) Lifetime proteomic profiling of an A30P alpha-synuclein Drosophila model of Parkinson's disease. J. Proteome Res. 6, 3729-3738) that defects in cellular components such as actin cytoskeleton and mitochondria may contribute to the development of later symptoms.
一种结合多维液相色谱和串联质谱的全局同位素标记策略被用于帕金森病(PD)的症状前A53Tα-突触核蛋白果蝇模型的定量蛋白质组分析。将不同浓度比例的多种内标蛋白加入到来自帕金森病样动物和对照动物的样本中,以评估定量准确性。分析了正向和反向同位素标记的两个生物学重复样本。总共对253种蛋白质进行了定量,每种蛋白质至少鉴定出两条肽序列;在正向和反向标记测量中均检测到180种(约71%)蛋白质。在A53Tα-突触核蛋白果蝇中有24种蛋白质差异表达;通过蛋白质印迹分析证实了肌钙蛋白T的上调和脂肪体蛋白1的下调。已知热休克蛋白70同源物3和ATP合酶的表达升高直接参与A53Tα-突触核蛋白介导的毒性作用和帕金森病;三种上调的蛋白质(60A处的肌肉LIM蛋白、锰超氧化物歧化酶和肌钙蛋白T)和两种下调的蛋白质(视蛋白和视网膜变性A)在文献中有与细胞功能障碍相关的报道。在症状前动物中观察到这些变化可能有助于揭示帕金森病的病因。蛋白质相互作用网络分析表明,七种蛋白质属于一个单一网络,这可能为深入了解帕金森病潜在的分子途径提供线索。基因本体分析表明,失调的蛋白质主要与膜、内质网、肌动蛋白细胞骨架、线粒体和核糖体相关。这些关联支持了在A30Pα-突触核蛋白果蝇模型研究中的先前发现(Xun, Z. Y., Sowell, R. A., Kaufman, T. C., and Clemmer, D. E. (2007) Protein expression in a Drosophila model of Parkinson's disease. J. Proteome Res. 6, 348 - 357; Xun, Z. Y., Sowell, R. A., Kaufman, T. C., and Clemmer, D. E. (2007) Lifetime proteomic profiling of an A30P alpha-synuclein Drosophila model of Parkinson's disease. J. Proteome Res. 6, 3729 - 3738),即肌动蛋白细胞骨架和线粒体等细胞成分的缺陷可能导致后期症状的发展。