The Institute of Chemistry, The Center for Nanoscience and Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
State Key Laboratory of Biogeology and Environmental Geology, Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, People's Republic of China.
ACS Nano. 2023 Aug 22;17(16):15308-15327. doi: 10.1021/acsnano.3c04415. Epub 2023 Aug 7.
Membrane fusion processes play key roles in biological transformations, such as endocytosis/exocytosis, signal transduction, neurotransmission, or viral infections, and substantial research efforts have been directed to emulate these functions by artificial means. The recognition and dynamic reconfiguration properties of nucleic acids provide a versatile means to induce membrane fusion. Here we address recent advances in the functionalization of liposomes or membranes with structurally engineered lipidated nucleic acids guiding the fusion of cell-like containments, and the biophysical and chemical parameters controlling the fusion of the liposomes will be discussed. Intermembrane bridging by duplex or triplex nucleic acids and light-induced activation of membrane-associated nucleic acid constituents provide the means for spatiotemporal fusion of liposomes or nucleic acid modified liposome fusion with native cell membranes. The membrane fusion processes lead to exchange of loads in the fused containments and are a means to integrate functional assemblies. This is exemplified with the operation of biocatalytic cascades and dynamic DNA polymerization/nicking or transcription machineries in fused protocell systems. Membrane fusion processes of protocell assemblies are found to have important drug-delivery, therapeutic, sensing, and biocatalytic applications. The future challenges and perspectives of DNA-guided fused containments and membranes are addressed.
膜融合过程在生物转化中起着关键作用,如内吞作用/外排作用、信号转导、神经传递或病毒感染,人们已经投入大量研究努力通过人工手段来模拟这些功能。核酸的识别和动态重构特性为诱导膜融合提供了一种通用的方法。在这里,我们将讨论最近在结构工程化的脂质化核酸功能化脂质体或膜方面的进展,这些核酸指导细胞样容器的融合,并且将讨论控制脂质体融合的生物物理和化学参数。双链体或三链体核酸的跨膜桥接以及光诱导的膜相关核酸成分的激活为脂质体或核酸修饰的脂质体与天然细胞膜的时空融合提供了手段。膜融合过程导致融合容器中负载的交换,并且是整合功能组件的一种手段。这可以通过在融合原细胞系统中生物催化级联和动态 DNA 聚合/切口或转录机制的操作来例证。原细胞组装的膜融合过程在药物输送、治疗、传感和生物催化应用中具有重要意义。本文还讨论了 DNA 引导的融合容器和膜的未来挑战和前景。