Exosome enrichment of human serum using multiple cycles of centrifugation

被引:66
作者
Kim, Jeongkwon [1 ]
Tan, Zhijing [2 ]
Lubman, David M. [2 ]
机构
[1] Chungnam Natl Univ, Dept Chem, Taejon 305764, South Korea
[2] Univ Michigan, Med Ctr, Dept Surg, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院; 新加坡国家研究基金会;
关键词
Centrifugation; Exosomes; Human serum; Mass spectrometry; Ultracentrifugation; PROTEOMIC ANALYSIS; URINARY EXOSOMES; HUMAN PLASMA; EXTRACELLULAR VESICLES; STEM-CELLS; SUBPOPULATIONS; IDENTIFICATION; APOPTOSIS; MICRORNA; ANTIGENS;
D O I
10.1002/elps.201500131
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, we compared the use of repeated cycles of centrifugation at conventional speeds for enrichment of exosomes from human serum compared to the use of ultracentrifugation (UC). After removal of cells and cell debris, a speed of 110000 x g or 40000 x g was used for the UC or centrifugation enrichment process, respectively. The enriched exosomes were analyzed using the bicinchoninic acid assay, 1D gel separation, transmission electron microscopy, Western blotting, and high-resolution LC-MS/MS analysis. It was found that a five-cycle repetition of UC or centrifugation is necessary for successful removal of nonexosomal proteins in the enrichment of exosomes from human serum. More significantly, 5x centrifugation enrichment was found to provide similar or better performance than 5x UC enrichment in terms of enriched exosome protein amount, Western blot band intensity for detection of CD-63, and numbers of identified exosome-related proteins and cluster of differentiation (CD) proteins. A total of 478 proteins were identified in the LC-MS/MS analyses of exosome proteins obtained from 5x UCs and 5x centrifugations including many important CD membrane proteins. The presence of previously reported exosome-related proteins including key exosome protein markers demonstrates the utility of this method for analysis of proteins in human serum.
引用
收藏
页码:2017 / 2026
页数:10
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