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应用16O/18O反向蛋白水解标记法测定生物膜培养对牙龈卟啉单胞菌W50细胞包膜蛋白质组的影响。

Application of 16O/18O reverse proteolytic labeling to determine the effect of biofilm culture on the cell envelope proteome of Porphyromonas gingivalis W50.

作者信息

Ang Ching-Seng, Veith Paul D, Dashper Stuart G, Reynolds Eric C

机构信息

Centre for Oral Health Science, School of Dental Science, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Australia.

出版信息

Proteomics. 2008 Apr;8(8):1645-60. doi: 10.1002/pmic.200700557.

Abstract

Porphyromonas gingivalis is an oral pathogen linked to chronic periodontitis. The bacterium exists as part of a polymicrobial biofilm accreted onto the tooth surface. An understanding of the changes to the proteome especially of the cell envelope of biofilm cells compared with planktonic cells could provide valuable insight into the molecular processes of biofilm formation. To establish which proteins changed in abundance between the planktonic and biofilm growth states, the cell envelope fractions of two biological replicates of P. gingivalis cultivated in a chemostat were analysed. Proteins were separated by 1-D SDS-PAGE, in-gel digested with trypsin in the presence of H216O or H218O and identified and quantified by LC-MALDI TOF/TOF-MS. Using a reverse labeling strategy we identified and quantified the changes in abundance of 81 P. gingivalis cell envelope proteins. No form of bias between the labels was observed. Twenty four proteins increased in abundance and 18 decreased in abundance in the biofilm state. A group of cell-surface located C-Terminal Domain family proteins including RgpA, HagA, CPG70 and PG99 increased in abundance in the biofilm cells. Other proteins that exhibited significant changes in abundance included transport related proteins (HmuY and IhtB), metabolic enzymes (FrdAB) and immunogenic proteins.

摘要

牙龈卟啉单胞菌是一种与慢性牙周炎相关的口腔病原体。该细菌作为附着在牙齿表面的多微生物生物膜的一部分而存在。了解生物膜细胞与浮游细胞相比蛋白质组尤其是细胞包膜的变化,可为生物膜形成的分子过程提供有价值的见解。为了确定浮游生长状态和生物膜生长状态之间哪些蛋白质的丰度发生了变化,对在恒化器中培养的牙龈卟啉单胞菌的两个生物学重复样本的细胞包膜部分进行了分析。蛋白质通过一维SDS-PAGE分离,在H216O或H218O存在下用胰蛋白酶进行胶内消化,并通过LC-MALDI TOF/TOF-MS进行鉴定和定量。使用反向标记策略,我们鉴定并定量了81种牙龈卟啉单胞菌细胞包膜蛋白丰度的变化。未观察到标记之间存在任何形式的偏差。在生物膜状态下,24种蛋白质的丰度增加,18种蛋白质的丰度降低。一组位于细胞表面的C末端结构域家族蛋白,包括RgpA、HagA、CPG70和PG99,在生物膜细胞中的丰度增加。其他丰度有显著变化的蛋白质包括转运相关蛋白(HmuY和IhtB)、代谢酶(FrdAB)和免疫原性蛋白。

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