Extracellular vesicles (EVs) are critical mediators of intercellular communication, and valuable sources of biomarkers for diagnostic and therapeutic applications. However, the complexity and heterogeneity of EVs present significant challenges for their proteomic characterization. Major challenges of EV samples include low yield, technical variability, and the need for sensitive and high throughput quantification approaches. In this study, we implement a tandem mass tag (TMT)-based MS workflow for comprehensive, quantitative proteomic profiling of isolated EVs. Through comparison with label-free quantitation (LFQ), we highlight the potential pitfalls and limitations of methodological choices in EV proteomic analyses. Our study integrates standard EV isolation with robust TMT labeling and high-resolution MS, providing insights into practical EV analysis. Utilizing this approach, we profiled EVs isolated from human fibroblasts treated with ionizing radiation. The TMT workflow uncovered an EV proteomic signature reflective of the cellular origins and potential functional roles of irradiated fibroblasts, compared to the LFQ workflow. Our case study underscores the potential of TMT-based MS to overcome common barriers in EV proteomics, facilitating new discoveries in EV biology and advancing their application in biomarker development and translational research.
Proteomics in Practice: A Case Study Highlighting Tandem Mass Tag-Based MS for Quantitative Profiling of Extracellular Vesicles and Application to Irradiated Fibroblasts.
阅读:3
作者:Berumen Sánchez Greg, Patel Purvi, Rose Kristie Lindsey, Rafat Marjan
| 期刊: | Proteomics | 影响因子: | 3.900 |
| 时间: | 2026 | 起止号: | 2026 Feb;26(2-3):163-177 |
| doi: | 10.1002/pmic.70103 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
