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用于尿液细胞外囊泡鉴定和蛋白质组分析的静水压过滤透析法与超速离心法的比较

Comparison of Hydrostatic Filtration Dialysis with Ultracentrifugation Methods for the Identification and Proteomic Profiling of Urinary Extracellular Vesicles.

作者信息

Chen Yunying, Hong Guobao, Wu Fan, Sheng Jieli, Zou Ziliang, Xiong Chongxiang, Zhang Ying, Jin Deng, Tang Hongjuan, Wang Xin, Zou Hequn

出版信息

Clin Lab. 2019 Apr 1;65(4). doi: 10.7754/Clin.Lab.2018.180922.

Abstract

BACKGROUND

Urinary extracellular vesicles (UEVs) carry rich markers of their parent cells, so they can serve as possible biomarkers of kidney diseases.

METHODS

In this study, we isolated urinary extracellular vesicles from five individuals using a simple, clinically applicable method called hydrostatic filtration dialysis (HFD) and compared it to the gold-standard ultracentrifuga-tion (UC) with transmission electron microscopy (TEM). We also employed a proteomic approach using pooled human urine samples from the same five individuals to profile the protein composition of UEVs to evaluate the effectiveness of these two methods.

RESULTS

Notably, using TEM, we found that all isolations contained 0 - 400 nm vesicles with the traditionally reported morphology, although the TEM results showed that the UEVs isolated from HFD compared to those from UC are larger and more extensive. We obtained a total of 2,564 UEV proteins in the two methods. We showed a large overlap (2,185 > 85%) between the proteins identified by both isolation methods. The result also showed that the obtained proteins in extracellular vesicles, which are isolated with these methods, are consistent with the results in currently available databases. However, in the associated gene ontologies, the enriched proteins found by the two methods showed some differences.

CONCLUSIONS

The HFD method is clinically feasible and allows large-scale protein profiling of UEV biomarkers. The results of this study also provide valuable UEV protein data from the methodological comparison, which might be valuable to other researchers.

摘要

背景

尿细胞外囊泡(UEVs)携带其母细胞的丰富标志物,因此可作为肾脏疾病的潜在生物标志物。

方法

在本研究中,我们使用一种简单的、临床适用的方法——静水压过滤透析(HFD),从五名个体中分离尿细胞外囊泡,并通过透射电子显微镜(TEM)将其与金标准超速离心法(UC)进行比较。我们还采用蛋白质组学方法,使用来自相同五名个体的混合人尿样本,对UEVs的蛋白质组成进行分析,以评估这两种方法的有效性。

结果

值得注意的是,通过透射电子显微镜观察,我们发现所有分离物均含有0-400nm的囊泡,具有传统报道的形态,尽管透射电子显微镜结果显示,与UC法分离的UEVs相比,HFD法分离的UEVs更大且更广泛。我们在两种方法中总共获得了2564种UEV蛋白。我们发现两种分离方法鉴定出的蛋白质之间有很大的重叠(2185种,>85%)。结果还表明,用这些方法分离的细胞外囊泡中获得的蛋白质与现有数据库中的结果一致。然而,在相关的基因本体论中,两种方法发现的富集蛋白存在一些差异。

结论

HFD方法在临床上可行,可对UEV生物标志物进行大规模蛋白质分析。本研究结果还提供了来自方法学比较的有价值的UEV蛋白质数据,这可能对其他研究人员有价值。

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