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Rapid Isolation of Extracellular Vesicles from Cell Culture and Biological Fluids Using a Synthetic Peptide with Specific Affinity for Heat Shock Proteins

机译:使用对热休克蛋白具有特定亲和力的合成肽从细胞培养物和生物液中快速分离细胞外囊泡

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摘要

Recent studies indicate that extracellular vesicles are an important source material for many clinical applications, including minimally-invasive disease diagnosis. However, challenges for rapid and simple extracellular vesicle collection have hindered their application. We have developed and validated a novel class of peptides (which we named venceremin, or Vn) that exhibit nucleotide-independent specific affinity for canonical heat shock proteins. The Vn peptides were validated to specifically and efficiently capture HSP-containing extracellular vesicles from cell culture growth media, plasma, and urine by electron microscopy, atomic force microscopy, sequencing of nucleic acid cargo, proteomic profiling, immunoblotting, and nanoparticle tracking analysis. All of these analyses confirmed the material captured by the Vn peptides was comparable to those purified by the standard ultracentrifugation method. We show that the Vn peptides are a useful tool for the rapid isolation of extracellular vesicles using standard laboratory equipment. Moreover, the Vn peptides are adaptable to diverse platforms and therefore represent an excellent solution to the challenge of extracellular vesicle isolation for research and clinical applications.
机译:最近的研究表明,细胞外囊泡是许多临床应用(包括微创疾病诊断)的重要来源。然而,快速和简单的细胞外囊泡收集的挑战阻碍了它们的应用。我们已经开发并验证了一类新型肽(我们称其为venceremin或Vn),它们对典型的热激蛋白表现出不依赖核苷酸的特异性亲和力。通过电子显微镜,原子力显微镜,核酸货物测序,蛋白质组分析,免疫印迹和纳米颗粒跟踪分析,验证了Vn肽可从细胞培养生长培养基,血浆和尿液中特异性有效地捕获含HSP的细胞外囊泡。所有这些分析证实了Vn肽捕获的物质与通过标准超速离心方法纯化的物质相当。我们显示,Vn肽是使用标准实验室设备快速分离细胞外囊泡的有用工具。此外,Vn肽可适应多种平台,因此代表了针对研究和临床应用的细胞外囊泡分离挑战的绝佳解决方案。

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