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牙龈卟啉单胞菌细胞内定量蛋白质组学

Quantitative proteomics of intracellular Porphyromonas gingivalis.

作者信息

Xia Qiangwei, Wang Tiansong, Taub Fred, Park Yoonsuk, Capestany Cindy A, Lamont Richard J, Hackett Murray

机构信息

Department of Chemical Engineering, University of Washington, Seattle, WA 98195, USA.

出版信息

Proteomics. 2007 Dec;7(23):4323-37. doi: 10.1002/pmic.200700543.

Abstract

Whole-cell quantitative proteomic analyses were conducted to investigate the change from an extracellular to intracellular lifestyle for Porphyromonas gingivalis, a Gram-negative intracellular pathogen associated with periodontal disease. Global protein abundance data for P. gingivalis strain ATCC 33277 internalized for 18 h within human gingival epithelial cells and controls exposed to gingival cell culture medium were obtained at sufficient coverage to provide strong evidence that these changes are profound. A total of 385 proteins were overexpressed in internalized P. gingivalis relative to controls; 240 proteins were shown to be underexpressed. This represented in total about 28% of the protein encoding ORFs annotated for this organism, and slightly less than half of the proteins that were observed experimentally. Production of several proteases, including the classical virulence factors RgpA, RgpB, and Kgp, was decreased. A separate validation study was carried out in which a 16-fold dilution of the P. gingivalis proteome was compared to the undiluted sample in order to assess the quantitative false negative rate (all ratios truly alternative). Truly null (no change) abundance ratios from technical replicates were used to assess the rate of quantitative false positives over the entire proteome. A global comparison between the direction of abundance change observed and previously published bioinformatic gene pair predictions for P. gingivalis will assist with future studies of P. gingivalis gene regulation and operon prediction.

摘要

进行全细胞定量蛋白质组分析,以研究牙龈卟啉单胞菌从细胞外生活方式转变为细胞内生活方式的变化。牙龈卟啉单胞菌是一种与牙周疾病相关的革兰氏阴性细胞内病原体。获得了牙龈卟啉单胞菌菌株ATCC 33277在人牙龈上皮细胞内化18小时后的整体蛋白质丰度数据,以及暴露于牙龈细胞培养基的对照数据,其覆盖范围足以提供有力证据证明这些变化是深刻的。相对于对照,共有385种蛋白质在内化的牙龈卟啉单胞菌中过表达;有240种蛋白质表达不足。这总共约占该生物体注释的蛋白质编码开放阅读框的28%,略少于实验观察到的蛋白质的一半。包括经典毒力因子RgpA、RgpB和Kgp在内的几种蛋白酶的产生减少。进行了一项单独的验证研究,将牙龈卟啉单胞菌蛋白质组稀释16倍后的样品与未稀释样品进行比较,以评估定量假阴性率(所有比率均为真正的差异)。来自技术重复的真正无变化(无变化)丰度比率用于评估整个蛋白质组的定量假阳性率。观察到的丰度变化方向与先前发表的牙龈卟啉单胞菌生物信息学基因对预测之间的全局比较,将有助于未来对牙龈卟啉单胞菌基因调控和操纵子预测的研究。

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