Morandi Mattia I, Busko Petro, Ozer-Partuk Efrat, Khan Suman, Zarfati Giulia, Elbaz-Alon Yael, Abou Karam Paula, Napso Shogan Tina, Ginini Lana, Gil Ziv, Regev-Rudzki Neta, Avinoam Ori
Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 7610001, Israel.
Faculty of Health, Bar Ilan University, Ramat-Gan 5290002, Israel.
PNAS Nexus. 2022 Aug 16;1(4):pgac156. doi: 10.1093/pnasnexus/pgac156. eCollection 2022 Sep.
Extracellular vesicles (EVs) transfer bioactive molecules between cells in a process reminiscent of enveloped viruses. EV cargo delivery is thought to occur by protein-mediated and pH-dependent membrane fusion of the EV and the cellular membrane. However, there is a lack of methods to identify the fusion proteins and resolve their mechanism. We developed and benchmarked an biophysical assay to investigate EV membrane fusion. The assay was standardized by directly comparing EV and viral fusion with liposomes. We show that EVs and retroviruses fuse with liposomes mimicking the membrane composition of the late endosome in a pH- and protein-dependent manner. Moreover, we directly visualize the stages of membrane fusion using cryo-electron tomography. We find that, unlike most retroviruses, EVs remain fusogenic after acidification and reneutralization. These results provide novel insights into the EV cargo delivery mechanism and an experimental approach to identify the EV fusion machinery.
细胞外囊泡(EVs)在细胞间传递生物活性分子,这一过程类似于包膜病毒。EVs的货物递送被认为是通过蛋白质介导的、依赖pH的EV与细胞膜的膜融合来实现的。然而,目前缺乏识别融合蛋白并解析其机制的方法。我们开发并验证了一种生物物理检测方法来研究EV膜融合。该检测方法通过直接比较EV和病毒与脂质体的融合进行了标准化。我们发现,EVs和逆转录病毒以pH和蛋白质依赖的方式与模拟晚期内体膜组成的脂质体融合。此外,我们使用冷冻电子断层扫描直接观察膜融合的各个阶段。我们发现,与大多数逆转录病毒不同,EVs在酸化和再中和后仍具有融合活性。这些结果为EV货物递送机制提供了新的见解,并为识别EV融合机制提供了一种实验方法。