Nanomechanical action opens endo-lysosomal compartments

• Published in: Nature communications Vol. 14; no. 1; pp. 6645 - 11
• Main Authors: Zhao, Yu, Ye, Zhongfeng, Song, Donghui, Wich, Douglas, Gao, Shuliang, Khirallah, Jennifer, Xu, Qiaobing
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20.10.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 42; 631/61/54; 631/67/1059; 639/166/985; 639/301/54; 639/638/439; Animals; Anticancer properties; Antigen (tumor-associated); Antigens; Azo compounds; Biological products; Biological Products - metabolism; Biological Transport; Compartments; Cytoplasm; Dendritic cells; Destabilization; Humanities and Social Sciences; Intracellular; Irradiation; Light; Light irradiation; Lipids; Lysosomes - metabolism; Melanoma; Membranes; Mice; Molecular machines; multidisciplinary; Nucleic acids; Photons; Proteins; Radiation; Science; Science (multidisciplinary); Ultraviolet radiation
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-023-42280-9

Endo-lysosomal escape is a highly inefficient process, which is a bottleneck for intracellular delivery of biologics, including proteins and nucleic acids. Herein, we demonstrate the design of a lipid-based nanoscale molecular machine, which achieves efficient cytosolic transport of biologics by destabilizing endo-lysosomal compartments through nanomechanical action upon light irradiation. We fabricate lipid-based nanoscale molecular machines, which are designed to perform mechanical movement by consuming photons, by co-assembling azobenzene lipidoids with helper lipids. We show that lipid-based nanoscale molecular machines adhere onto the endo-lysosomal membrane after entering cells. We demonstrate that continuous rotation-inversion movement of Azo lipidoids triggered by ultraviolet/visible irradiation results in the destabilization of the membranes, thereby transporting cargoes, such as mRNAs and Cre proteins, to the cytoplasm. We find that the efficiency of cytosolic transport is improved about 2.1-fold, compared to conventional intracellular delivery systems. Finally, we show that lipid-based nanoscale molecular machines are competent for cytosolic transport of tumour antigens into dendritic cells, which induce robust antitumour activity in a melanoma mouse model. Endo-lysosomal escape is a highly inefficient process. Here the authors present a lipid-based nanoscale molecular machine that achieves efficient cytosolic transport of biologics by destabilizing endo-lysosomal compartments through nanomechanical action upon light irradiation.