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缓冲密度梯度超速离心(C-DGUC)提高了细胞外囊泡的分离效率。

Cushioned-Density Gradient Ultracentrifugation (C-DGUC) improves the isolation efficiency of extracellular vesicles.

机构信息

Surgical Service San Francisco VA Medical Center, San Francisco, California, United States of America.

Division of Vascular and Endovascular Surgery, Department of Surgery, University of California, San Francisco, California, United States of America.

出版信息

PLoS One. 2019 Apr 11;14(4):e0215324. doi: 10.1371/journal.pone.0215324. eCollection 2019.

Abstract

Ultracentrifugation (UC) is recognized as a robust approach for the isolation of extracellular vesicles (EVs). However, recent studies have highlighted limitations of UC including low recovery efficiencies and aggregation of EVs that could impact downstream functional analyses. We tested the benefit of using a liquid cushion of iodixanol during UC to address such shortcomings. In this study, we compared the yield and purity of EVs isolated from J774A.1 macrophage conditioned media by conventional UC and cushioned-UC (C-UC). We extended our study to include two other common EV isolation approaches: ultrafiltration (UF) and polyethylene glycol (PEG) sedimentation. After concentrating EVs using these four methods, the concentrates underwent further purification by using OptiPrep density gradient ultracentrifugation (DGUC). Our data show that C-DGUC provides a two-fold improvement in EV recovery over conventional UC-DGUC. We also found that UF-DGUC retained ten-fold more protein while PEG-DGUC achieved similar performance in nanoparticle and protein recovery compared to C-DGUC. Regarding purity as assessed by nanoparticle to protein ratio, our data show that EVs isolated by UC-DGUC achieved the highest purity while C-DGUC and PEG-DGUC led to similarly pure preparations. Collectively, we demonstrate that the use of a high-density iodixanol cushion during the initial concentration step improves the yield of EVs derived from cell culture media compared to conventional UC. This enhanced yield without substantial retention of protein contaminants and without exposure to forces causing aggregation offers new opportunities for the isolation of EVs that can subsequently be used for functional studies.

摘要

超速离心(UC)被认为是分离细胞外囊泡(EVs)的一种强大方法。然而,最近的研究强调了 UC 的局限性,包括回收率低和 EV 聚集,这可能会影响下游的功能分析。我们测试了在 UC 过程中使用碘克沙醇液体垫来解决这些缺点的益处。在这项研究中,我们比较了通过常规 UC 和垫 UC(C-UC)从 J774A.1 巨噬细胞条件培养基中分离的 EV 的产量和纯度。我们将研究扩展到包括另外两种常见的 EV 分离方法:超滤(UF)和聚乙二醇(PEG)沉淀。使用这四种方法浓缩 EV 后,通过使用 OptiPrep 密度梯度超速离心(DGUC)进一步纯化浓缩物。我们的数据表明,C-DGUC 比常规 UC-DGUC 提高了 EV 回收率两倍。我们还发现 UF-DGUC 保留了十倍以上的蛋白质,而 PEG-DGUC 在纳米颗粒和蛋白质回收率方面与 C-DGUC 相比具有相似的性能。关于通过纳米颗粒与蛋白质比值评估的纯度,我们的数据表明,通过 UC-DGUC 分离的 EV 具有最高的纯度,而 C-DGUC 和 PEG-DGUC 导致类似纯度的制备物。总的来说,我们证明了在初始浓缩步骤中使用高密度碘克沙醇垫可以提高从细胞培养基中分离 EV 的产量,与常规 UC 相比。这种增强的产量没有实质性保留蛋白质污染物,并且没有暴露于导致聚集的力,为 EV 的分离提供了新的机会,随后可以用于功能研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2310/6459479/ca8c93d96d2d/pone.0215324.g001.jpg

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