Department of Chemistry and Biochemistry and Ohio State Biochemistry Program, The Ohio State University, 484 West 12th Avenue, Columbus, Ohio 43210, United States.
Acc Chem Res. 2022 Feb 1;55(3):309-318. doi: 10.1021/acs.accounts.1c00560. Epub 2022 Jan 11.
Biomolecules such as peptides, proteins, and nucleic acids generally cannot cross a cell membrane by passive diffusion. Nevertheless, cell-penetrating peptides (CPPs), bacterial protein toxins, certain eukaryotic proteins, viruses, and many synthetic drug delivery vehicles have been shown to enter the cytosol of eukaryotic cells with varying efficiencies. They generally enter the cell by one or more of the endocytic mechanisms and are initially localized inside the endosomes. But how they cross the endosomal membrane to reach the cytosol (i.e., endosomal escape) has been a mystery for decades, and this knowledge gap has been a major bottleneck for the development of efficient drug delivery systems. In addition, many bacterial and eukaryotic proteins are transported across the plasma membrane in their native states into the periplasmic/extracellular space through the twin-arginine translocation (TAT) and unconventional protein secretion (UPS) systems, respectively. Again, the mechanisms underpinning these protein export systems remain unclear.In this Account, I introduce a previously unrecognized, fundamental membrane translocation mechanism which we have termed the vesicle budding-and-collapse (VBC) mechanism. Through VBC, biomolecules of diverse sizes and physicochemical properties autonomously translocate across cell membranes topologically (i.e., from one side to the other side of the membrane) but not physically (i.e., without going through the membrane). We have demonstrated that CPPs and bacterial protein toxins escape the endosome by the VBC mechanism in giant unilamellar vesicles as well as live mammalian cells. This advance resulted from studies in which we labeled the biomolecules with a pH-sensitive, red-colored dye (pHAb) and phosphatidylserine with a pH-insensitive green dye (TopFluor) and monitored the intracellular trafficking of the biomolecules in real time by confocal microscopy. In addition, by enlarging the endosomes with a kinase inhibitor, we were able to visualize the structural changes of the endosomes (i.e., endosomal escape intermediates) as they went through the VBC process. I postulate that bacterial/viral/eukaryotic proteins, nonenveloped viruses, and synthetic drug delivery vehicles (e.g., polyplexes, lipoplexes, and lipid nanoparticles) may also escape the endosome by inducing VBC. Furthermore, I propose that VBC may be the mechanism that drives the bacterial TAT and eukaryotic UPS systems. Our findings fill a long-standing gap in cell biology and provide guiding principles for designing more efficient drug delivery vehicles.
生物分子,如肽、蛋白质和核酸,一般不能通过被动扩散穿过细胞膜。然而,细胞穿透肽 (CPP)、细菌蛋白毒素、某些真核蛋白、病毒和许多合成药物递送载体已被证明能够以不同的效率进入真核细胞的细胞质。它们通常通过一种或多种内吞作用机制进入细胞,最初定位于内体内部。但是,它们如何穿过内体膜到达细胞质(即内体逃逸)几十年来一直是一个谜,而这一知识空白一直是开发高效药物递送系统的主要瓶颈。此外,许多细菌和真核蛋白以其天然状态通过双精氨酸转运 (TAT) 和非常规蛋白分泌 (UPS) 系统分别穿过质膜进入周质/细胞外空间。同样,这些蛋白输出系统的机制仍不清楚。在本综述中,我介绍了一个以前未被认识到的基本膜转运机制,我们称之为囊泡出芽和塌陷 (VBC) 机制。通过 VBC,大小和物理化学性质不同的生物分子能够自主拓扑地(即从膜的一侧到另一侧)而不是物理地(即不穿过膜)穿过细胞膜。我们已经证明 CPP 和细菌蛋白毒素通过 VBC 机制从巨单层囊泡以及活哺乳动物细胞中逃逸内体。这一进展是通过用 pH 敏感的红色染料 (pHAb) 标记生物分子和用 pH 不敏感的绿色染料 (TopFluor) 标记磷脂酰丝氨酸,并通过共聚焦显微镜实时监测生物分子的细胞内转运而实现的。此外,通过用激酶抑制剂扩大内体,我们能够观察到内体的结构变化(即内体逃逸中间体),因为它们经历了 VBC 过程。我推测,细菌/病毒/真核蛋白、无包膜病毒和合成药物递送载体(例如,多聚物、脂多聚物和脂质纳米颗粒)也可能通过诱导 VBC 来逃避内体。此外,我提出 VBC 可能是驱动细菌 TAT 和真核 UPS 系统的机制。我们的发现填补了细胞生物学中的一个长期空白,并为设计更高效的药物递送载体提供了指导原则。