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使用聚酯、毛细管通道聚合物纤维柱中的吐温-20 洗脱溶剂从人尿中分离和定量外泌体。

Isolation and quantification of human urinary exosomes using a Tween-20 elution solvent from polyester, capillary-channeled polymer fiber columns.

机构信息

Department of Chemistry, Biosystems Research Complex, Clemson University, Clemson, SC, 29634-0973, USA.

Department of Chemistry, Biosystems Research Complex, Clemson University, Clemson, SC, 29634-0973, USA.

出版信息

Anal Chim Acta. 2024 Nov 15;1329:343242. doi: 10.1016/j.aca.2024.343242. Epub 2024 Sep 12.

Abstract

BACKGROUND

Exosomes, a subset of extracellular vesicles (EVs), are a type of membrane-secreted vesicle essential for intercellular communication. There is a great deal of interest in developing methods to isolate and quantify exosomes to study their role in intercellular processes and as potential therapeutic delivery systems. Polyester, capillary-channeled polymer fiber columns and spin-down tips are highly efficient, low-cost means of exosome isolation. As the methodology evolves, there remain questions as to the optimum elution solvent for specific end-uses of the recovered vesicles; fundamental biochemistry, clinical diagnostics, or therapeutic vectors.

RESULTS

While both acetonitrile and glycerol have been proven highly successful in terms of EV recoveries in the hydrophobic interaction chromatography workflow, many biological studies entail the use of the non-ionic detergent, Tween-20, as a working solvent. Here we evaluate the use of Tween-20 as the elution solvent for the recovery of exosomes. A novel 10-min, two-step gradient elution method, employing 0.1 % v/v Tween-20, efficiently isolated EVs at a concentration of ∼10 EV mL from a 100 μL urine injection. Integration of absorbance and multi-angle light scattering detectors in standard HPLC instrumentation enables a comprehensive single-injection determination of eluted exosome concentration and sizes. Transmission electron microscopy verifies the retention of the vesicular structure of the exosomes. The micro-bicinchoninic acid protein quantification assay confirmed high-purity isolations of exosomes (∼99 % removal of background proteins) SIGNIFICANCE: The effective use of Tween-20 as an elution solvent for exosome isolation/purification using capillary-channeled polymer fiber columns adds greater versatility to the portfolio of the approach. The proposed method holds promise for a wide range of fundamental biochemistry, clinical diagnostics, and therapeutic applications, marking a significant advancement in EV-based methodologies.

摘要

背景

外泌体是细胞外囊泡 (EV) 的一个子集,是细胞间通讯所必需的一种膜分泌囊泡。开发分离和定量外泌体的方法来研究它们在细胞间过程中的作用以及作为潜在的治疗性递药系统的方法引起了广泛关注。聚酯、毛细管通道聚合物纤维柱和离心管 tips 是高效、低成本的外泌体分离方法。随着方法的不断发展,对于回收囊泡的特定用途(基础生物化学、临床诊断或治疗载体),仍然存在最佳洗脱溶剂的问题。

结果

虽然乙腈和甘油在疏水性相互作用色谱工作流程中都被证明在外泌体回收方面非常成功,但许多生物学研究都需要使用非离子型洗涤剂吐温-20 作为工作溶剂。在这里,我们评估了使用吐温-20 作为洗脱溶剂来回收外泌体。一种新颖的 10 分钟、两步梯度洗脱方法,采用 0.1% v/v 吐温-20,能够有效地从 100μL 尿液注射中以约 10 EV mL 的浓度分离 EV。在标准 HPLC 仪器中集成吸光度和多角度光散射检测器,可实现洗脱外泌体浓度和大小的综合单次进样测定。透射电子显微镜验证了保留了外泌体的囊泡结构。微量 bicinchoninic 酸蛋白定量测定证实了外泌体的高纯度分离(去除背景蛋白约 99%)。

意义

使用毛细管通道聚合物纤维柱将吐温-20 有效用作外泌体分离/纯化的洗脱溶剂,为该方法增加了更大的多功能性。所提出的方法有望在广泛的基础生物化学、临床诊断和治疗应用中得到应用,标志着基于外泌体的方法取得了重大进展。

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