Pauwels Jarne, Van de Steene Tessa, De Muyer Freya, De Pauw Danaë, Baeke Femke, Eyckerman Sven, Gevaert Kris
VIB-UGent Center for Medical Biotechnology, VIB, Ghent, Belgium.
Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
J Extracell Vesicles. 2025 Jul;14(7):e70103. doi: 10.1002/jev2.70103.
Extracellular vesicles (EVs), nanoscale vesicles that are secreted by cells, are critical mediators of intercellular communication and play a crucial role in diverse pathologies such as cancer development. Therefore, EVs are regarded as having high potential in the clinic, both for diagnostic and therapeutic applications. Unfortunately, EVs reside in complex biofluids and their consistent preparation at sufficient purity for mass spectrometry-based proteomics has proven to be challenging, especially when increased high-throughput is required. Here, we describe the incorporation of our previously reported filter-aided EV enrichment (FAEVEr) strategy for the separation of EVs from conditioned medium, from harvest to proteomic analysis completely to a streamlined 96-well format. We compared our approach with ultracentrifugation, the most widely used method for EV enrichment, in terms of protein identifications, consistency, reproducibility and overall performance, including the invested time, resources and required expertise. In addition, our results show that including relative high percentages of Tween-20, a mild detergent, markedly improves the final purity of the EV proteome by removing the bulk of non-EV proteins (e.g., serum proteins) and significantly increases the number of identified transmembrane proteins. Moreover, our FAEVEr 96-well strategy improves the overall reproducibility with a consistent number of protein identifications and decreased number of missing values across replicates. This promotes the validity and comparability between results, which is essential in both a clinical and research setting, where consistency is paramount.
细胞外囊泡(EVs)是细胞分泌的纳米级囊泡,是细胞间通讯的关键介质,在癌症发展等多种病理过程中发挥着至关重要的作用。因此,EVs在临床诊断和治疗应用方面都被认为具有很高的潜力。不幸的是,EVs存在于复杂的生物流体中,要以足够的纯度持续制备用于基于质谱的蛋白质组学分析的EVs已被证明具有挑战性,尤其是在需要提高高通量的情况下。在这里,我们描述了将我们之前报道的滤膜辅助EV富集(FAEVEr)策略从收获到蛋白质组学分析完全整合到一个简化的96孔板形式中,用于从条件培养基中分离EVs。我们在蛋白质鉴定、一致性、可重复性和整体性能(包括投入的时间、资源和所需的专业知识)方面,将我们的方法与最广泛使用的EV富集方法——超速离心法进行了比较。此外,我们的结果表明,加入相对高比例的温和去污剂吐温-20,通过去除大部分非EV蛋白(如血清蛋白),显著提高了EV蛋白质组的最终纯度,并显著增加了鉴定出的跨膜蛋白数量。而且,我们的FAEVEr 96孔板策略提高了整体可重复性,蛋白质鉴定数量一致,重复样本中缺失值数量减少。这促进了结果之间的有效性和可比性,这在临床和研究环境中都是至关重要的,因为一致性是至关重要的。