College of Engineering and Applied Sciences, MOE Key Laboratory of High Performance Polymer Materials & Technology, Nanjing University, Nanjing, 210033, China.
Center for Soft Condensed Matter Physics and Interdisciplinary Research, School of Physical Science and Technology, Soochow University, Suzhou, 215031, China.
ACS Nano. 2024 Jan 23;18(3):2162-2183. doi: 10.1021/acsnano.3c09452. Epub 2024 Jan 10.
Neutral nanomaterials functionalized with PEG or similar molecules have been popularly employed as nanomedicines. Compared to positive counterparts that are capable of harnessing the well-known proton sponge effect to facilitate their escape from lysosomes, it is yet unclear how neutral substances got their entry into the cytosol. In this study, by taking PEGylated, neutral Au nanospheres as an example, we systematically investigated their time-dependent translocation postuptake. Specifically, we harnessed dissipative particle dynamics simulations to uncover how nanospheres bypass lysosomal entrapment, wherein a mechanism termed as "squeezing-out" mode was discovered. We next conducted a comprehensive investigation on how nanomaterials implicate lysosomes in terms of integrity and functionality. By using single-molecule imaging, specific preservation of PEG-terminated with targeting moieties in lysosomes supports the "squeezing-out" mode as the mechanism underlying the lysosomal escape of nanomaterials. All evidence points out that such a process is benign to lysosomes, wherein the escape of nanomaterials proceeds at the expense of targeting moieties loss. Furthermore, we proved that by fine-tuning of the efficacy of nanomaterials escaping from lysosomes, modulation of distinct pathways and metabolic machinery can be achieved readily, thereby offering us a simple and robust tool to implicate cells.
经聚乙二醇(PEG)或类似分子功能化的中性纳米材料已被广泛用作纳米药物。与能够利用众所周知的质子海绵效应促进其从溶酶体逃逸的正对照物相比,中性物质如何进入细胞质尚不清楚。在这项研究中,我们以 PEG 修饰的中性 Au 纳米球为例,系统地研究了它们摄取后的时间依赖性转位。具体来说,我们利用耗散粒子动力学模拟揭示了纳米球如何绕过溶酶体的捕获,其中发现了一种称为“挤出”模式的机制。接下来,我们全面研究了纳米材料如何影响溶酶体的完整性和功能。通过使用单分子成像,靶向基团封端的 PEG 在溶酶体中的特异性保留支持了“挤出”模式是纳米材料溶酶体逃逸的机制。所有证据都表明,这样的过程对溶酶体是良性的,纳米材料的逃逸是以靶向基团损失为代价的。此外,我们证明通过精细调整纳米材料从溶酶体逃逸的效果,可以轻松实现对不同途径和代谢机制的调节,从而为我们提供了一种简单而强大的工具来干预细胞。