Reinsalu Olavi, Samel Anneli, Niemeister Elen, Kurg Reet
Institute of Technology, University of Tartu, 50411 Tartu, Estonia.
Int J Mol Sci. 2021 May 14;22(10):5208. doi: 10.3390/ijms22105208.
Extracellular vesicles (EVs) are valued candidates for the development of new tools for medical applications. Vesicles carrying melanoma-associated antigen A (MAGEA) proteins, a subfamily of cancer-testis antigens, are particularly promising tools in the fight against cancer. Here, we have studied the biophysical and chemical properties of MAGEA4-EVs and show that they are stable under common storage conditions such as keeping at +4 °C and -80 °C for at least 3 weeks after purification. The MAGEA4-EVs can be freeze-thawed two times without losing MAGEA4 in detectable quantities. The attachment of MAGEA4 to the surface of EVs cannot be disrupted by high salt concentrations or chelators, but the vesicles are sensitive to high pH. The MAGEA4 protein can bind to the surface of EVs in vitro, using robust passive incubation. In addition, EVs can be loaded with recombinant proteins fused to the MAGEA4 open reading frame within the cells and also in vitro. The high stability of MAGEA4-EVs ensures their potential for the development of EV-based anti-cancer applications.
细胞外囊泡(EVs)是开发新型医学应用工具的理想候选者。携带黑色素瘤相关抗原A(MAGEA)蛋白(癌-睾丸抗原的一个亚家族)的囊泡,在抗癌斗争中是特别有前景的工具。在此,我们研究了MAGEA4-EVs的生物物理和化学性质,并表明它们在常见储存条件下是稳定的,例如纯化后在+4°C和-80°C保存至少3周。MAGEA4-EVs可以冻融两次而不会损失可检测量的MAGEA4。高盐浓度或螯合剂不会破坏MAGEA4与EVs表面的结合,但囊泡对高pH敏感。使用强力被动孵育,MAGEA4蛋白在体外可与EVs表面结合。此外,EVs可以在细胞内以及体外加载与MAGEA4开放阅读框融合的重组蛋白。MAGEA4-EVs的高稳定性确保了它们在基于EVs的抗癌应用开发中的潜力。