使用吐温-20 洗脱溶剂从聚酯毛细管通道聚合物纤维柱中分离和定量人类尿液外泌体

IF 5.7 2区 化学 Q1 CHEMISTRY, ANALYTICAL Analytica Chimica Acta Pub Date : 2024-09-12 DOI:10.1016/j.aca.2024.343242
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引用次数: 0

摘要

外泌体是细胞外囊泡(EVs)的一个分支,是一种膜分泌囊泡,对细胞间的交流至关重要。人们对开发分离和量化外泌体的方法非常感兴趣,以研究它们在细胞间过程中的作用,并将其作为潜在的治疗递送系统。聚酯、毛细管通道聚合物纤维柱和旋降吸头是高效、低成本的外泌体分离方法。随着该方法的发展,对于回收囊泡的特定最终用途(基础生化、临床诊断或治疗载体),最佳洗脱溶剂的问题依然存在。在疏水相互作用色谱工作流程中,乙腈和甘油都被证明是非常成功的囊泡回收溶剂,但许多生物研究需要使用非离子洗涤剂吐温-20 作为工作溶剂。在此,我们评估了使用吐温-20 作为洗脱溶剂回收外泌体的情况。使用 0.1 % v/v Tween-20 的新型 10 分钟两步梯度洗脱法能从 100 μL 尿液注射液中有效分离出浓度为 10 ∼ 10 EV mL 的外泌体。将吸光度和多角度光散射检测器集成到标准的高效液相色谱仪中,一次进样即可全面测定洗脱的外泌体浓度和大小。透射电子显微镜验证了外泌体囊泡结构的保留。微双喹啉酸蛋白定量测定证实了外泌体的高纯度分离(背景蛋白去除率为99%)。 在使用毛细管通道聚合物纤维柱分离/纯化外泌体时,可有效地使用吐温-20作为洗脱溶剂,这为该方法的组合增加了更大的通用性。该方法有望广泛应用于基础生化、临床诊断和治疗领域,标志着基于外泌体的方法取得了重大进展。
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Isolation and quantification of human urinary exosomes using a Tween-20 elution solvent from polyester, capillary-channeled polymer fiber columns

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 ∼1011 EV mL−1 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.

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来源期刊
Analytica Chimica Acta
Analytica Chimica Acta 化学-分析化学
CiteScore
10.40
自引率
6.50%
发文量
1081
审稿时长
38 days
期刊介绍: Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.
期刊最新文献
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