LC-MS/MS分离粪便外膜小泡及蛋白质组学分析方法

Journal of proteomics & bioinformatics Pub Date : 2019-01-01 Epub Date: 2019-03-18 DOI:10.4172/0974-276X.1000494
Jing Wu, Mingrui An, Jianhui Zhu, Zhijing Tan, Grace Y Chen, Ryan W Stidham, David M Lubman
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引用次数: 6

摘要

外膜囊泡(omv)是由细菌分泌的纳米级球体,类似于大多数哺乳动物细胞类型分泌的外泌体囊泡。与许多研究侧重于优化从生物体液中富集外泌体的方法相比,很少有研究对粪便样本中的外膜囊泡进行研究。在此,我们开发了一个由膜过滤和多次超离心(UC)组成的管道,从粪便样本中分离omv进行蛋白质组学分析,其中需要多次超离心来去除污染物。通过iTRAQ标记定量蛋白质组学分析,比较了不同过滤尺寸(0.22 μm和0.45 μm)在富集omv和去除背景粪便物质方面的性能。与0.22 μm过滤器相比,使用0.45 μm过滤器获得的蛋白质产量略高,但没有从细菌中鉴定出额外的污染蛋白质。利用0.45 μm滤镜和UC的多个循环分离omv进行蛋白质组学分析。据我们所知,这是第一个从粪便样本中分析大量OMV蛋白的研究。这种能力可能有助于为了解宿主和微生物群之间的交流提供有价值的信息,这对预防癌症和疾病的发展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Method for Isolation and Proteomic Analysis of Outer Membrane Vesicles from Fecal Samples by LC-MS/MS.

A Method for Isolation and Proteomic Analysis of Outer Membrane Vesicles from Fecal Samples by LC-MS/MS.

A Method for Isolation and Proteomic Analysis of Outer Membrane Vesicles from Fecal Samples by LC-MS/MS.

A Method for Isolation and Proteomic Analysis of Outer Membrane Vesicles from Fecal Samples by LC-MS/MS.

Outer membrane vesicles (OMVs) are nanosized spheres secreted by bacteria that are similar to the vesicles known as exosomes, which are secreted by most mammalian cell types. In contrast to many studies focusing on optimizing methods for enriching exosomes from biological fluid, few studies have been conducted to investigate outer membrane vesicles from fecal samples. Herein, we have developed a pipeline comprised of membrane filtration and multiple cycles of ultracentrifugation (UC) to isolate OMVs from fecal samples for proteomics analysis, where multiple cycles of UC are required for removal of contaminants. By iTRAQ labeling quantitative proteomics analysis, different filter sizes (0.22 μm and 0.45 μm) were compared in terms of their performance in enriching OMVs and eliminating background fecal material. Using the 0.45 μm filter, a slightly higher protein yield was obtained but no additional contaminating proteins from bacteria were identified compared to those from the 0.22 μm filter. The 0.45 μm filter together with the multiple cycles of UC were thus used to isolate OMVs for proteomics analysis. To our knowledge, this is the first study profiling a large number of OMV proteins from fecal samples. Such capabilities may help provide valuable information in understanding the communication between the host and microbiota, which is critical in preventing cancer and disease development.

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