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Genomics Proteomics Bioinformatics. 2007 May;5(2):111-20. doi: 10.1016/S1672-0229(07)60021-7.
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Whole proteome analysis of post-translational modifications: applications of mass-spectrometry for proteogenomic annotation.翻译后修饰的全蛋白质组分析:质谱技术在蛋白质基因组注释中的应用
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Current two-dimensional electrophoresis technology for proteomics.当前用于蛋白质组学的二维电泳技术。
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30℃和 37℃培养的福氏志贺菌 2a 2457T 的蛋白质组。

The proteome of Shigella flexneri 2a 2457T grown at 30 and 37 degrees C.

机构信息

Beijing Institute of Biotechnology, State Key Laboratory of Pathogen and Biosecurity, 100071 Beijing, China.

出版信息

Mol Cell Proteomics. 2010 Jun;9(6):1209-20. doi: 10.1074/mcp.M900446-MCP200. Epub 2010 Feb 17.

DOI:10.1074/mcp.M900446-MCP200
PMID:20164057
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2877981/
Abstract

To upgrade the proteome reference map of Shigella flexneri 2a 2457T, the protein expression profiles of log phase and stationary phase cells grown at 30 and 37 degrees C were thoroughly analyzed using multiple overlapping narrow pH range (between pH 4.0 and 11.0) two-dimensional gel electrophoresis. A total of 723 spots representing 574 protein entries were identified by MALDI-TOF/TOF MS, including the majority of known key virulence factors. 64 hypothetical proteins and six misannotated proteins were also experimentally identified. A comparison between the four proteome maps showed that most of the virulence-related proteins were up-regulated at 37 degrees C, and the differences were more notable in stationary phase cells, suggesting that the expressions of these virulence factors were not only controlled by temperature but also controlled by the nutrients available in the environment. The expression patterns of some virulence-related genes under the four different conditions suggested that they might also be regulated at the post-transcriptional level. A further significant finding was that the expression of the protein ArgT was dramatically up-regulated at 30 degrees C. The results of semiquantitative RT-PCR analysis showed that expression of argT was not regulated at the transcriptional level. Therefore, we carried out a series of experiments to uncover the mechanism regulating ArgT levels and found that the differential expression of ArgT was due to its degradation by a periplasmic protease, HtrA, whose activity, but not its synthesis, was affected by temperature. The cleavage site in ArgT was between position 160 (Val) and position 161 (Ala). These results may provide useful insights for understanding the physiology and pathogenesis of S. flexneri.

摘要

为了升级福氏志贺菌 2a 2457T 的蛋白质组参考图谱,我们使用多个重叠的窄 pH 范围(pH4.0 至 11.0)二维凝胶电泳,全面分析了在 30°C 和 37°C 下生长的对数期和静止期细胞的蛋白质表达谱。通过 MALDI-TOF/TOF MS 鉴定了总共 723 个斑点,代表 574 种蛋白质条目,其中包括大多数已知的关键毒力因子。还通过实验鉴定了 64 个假设蛋白和 6 个错误注释蛋白。将这四个蛋白质组图谱进行比较后发现,大多数与毒力相关的蛋白质在 37°C 时上调,在静止期细胞中的差异更为显著,这表明这些毒力因子的表达不仅受温度控制,还受环境中可用营养物质的控制。在四种不同条件下,一些与毒力相关的基因的表达模式表明,它们可能还受到转录后水平的调控。进一步的重要发现是,ArgT 蛋白的表达在 30°C 时显著上调。半定量 RT-PCR 分析结果表明,argT 的表达不受转录水平调控。因此,我们进行了一系列实验以揭示调节 ArgT 水平的机制,发现 ArgT 的差异表达是由于其被周质蛋白酶 HtrA 降解所致,而 HtrA 的活性(而非其合成)受温度影响。ArgT 中的切割位点位于第 160 位(缬氨酸)和第 161 位(丙氨酸)之间。这些结果可能为理解福氏志贺菌的生理学和发病机制提供有用的见解。