Release Subtitle:
Researchers have devised light-induced disruptive liposomes, optically controllable carriers that enable precise control of substance delivery inside cells

Release Summary Text:
Proteoliposomes, specialized systems capable of accommodating a wide range of molecules, have emerged as effective carriers for intracellular substance delivery. Recently, researchers from Okayama University and Hokkaido University in Japan developed Light-induced disruptive liposome (LiDL), an innovative nanomaterial that enables precise control of content release through light activation. LiDLs offer a promising solution as optically controllable carriers for intracellular substance delivery.

Full text of release:
Artificial lipid bilayer vesicle liposomes, also called proteoliposomes, are specialized systems capable of incorporating various molecules, such as chemicals and drugs. Their unique properties make them ideal carriers for delivering substances inside cells. However, they must possess the dual characteristics of high stability in extracellular environments and low stability in intracellular environments.

Several techniques have been developed to regulate the stability of liposomes in a condition-dependent manner, with pH-sensitive liposomes being widely employed. A standard measure of acidity or basicity, the pH scale ranges from 1 to 14, with 7 standing for “neutral,” like water, a pH below 7 indicating acidity and that above 7 indicating basicity. Interestingly, pH-sensitive liposomes can be triggered to release their contents when exposed to an acidic pH below 5.5.

In a new study, a team of researchers, led by Professor Yuki Sudo from Okayama University, Japan, have developed a precise method of releasing contents from pH-sensitive liposomes using light. “The study presents a novel nanomaterial called light-induced disruptive liposome (LiDL) and applies it to light-controlled intracellular substance delivery, ” explains Prof. Sudo. Their work, co-authored by Mr. Taichi Tsuneishi of Okayama University and Prof. Yuma Yamada of Hokkaido University in Japan, was published in Issue 59 of the journal Chemical Communications on 15 June 2023.

The researchers utilized a protein called Rubricoccus marinus Xenorhodopsin (RmXeR), derived from a marine bacterium, to initiate acidification inside liposomes using light. To study the functionality of RmXeR within liposomes without interference from pH-dependent properties, they first developed pH-insensitive proteoliposomes using the lipid hydration method, combining phosphatidylcholine from egg yolk with cholesterol. Then, purified RmXeR was incorporated via the dilution method. The researchers estimated that the pH inside the thus obtained liposomes changed from 7.0 to 4.8 upon exposure to green light, rendering them suitable for light-induced disruption.

Subsequently, the team developed pH-sensitive proteoliposomes based on 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine and cholesteryl hemisuccinate. Interestingly, before introducing RmXeR within the liposomes, the researchers incorporated a water-soluble fluorescent dye called calcein as a testing substance to evaluate their release capability. By monitoring the fluorescence of calcein, they observed that its release from the liposomes occurred in a light-dependent manner, indicating that the liposomes effectively released substances when triggered by light. These pH-sensitive proteoliposomes, or LiDLs, displayed exceptional stability in the absence of light, maintaining their physiochemical properties when exposed to a temperature of 4°C for two weeks.

In the next phase of the study, the researchers introduced LiDL into mammalian HeLa cells to evaluate their effectiveness as carriers for delivering substances inside the cells. They monitored the cellular uptake for LiDLs, finding that the presence of LiDL, regardless of the inclusion of RmXeR, enhanced the uptake of liposomes by HeLa cells. This demonstrated the potential of LiDL as a carrier for intracellular substance delivery. To further improve the intracellular delivery efficiency, the researchers introduced a chemical called stearyl octaarginine into LiDL. This enhanced version, called LiDL-R8, exhibited significantly better performance compared to LiDL.

These findings highlight the utility of LiDL for the intracellular delivery of chemicals as well as biomolecules. "With LiDL, drug delivery can be controlled by light, potentially leading to advances in various therapies," emphasizes Prof. Sudo. Going forward, the team aims to enhance the content release efficiency by thoroughly characterizing the structure of the liposomes and optimizing the experimental conditions.

In effect, LiDLs hold great promise as optically controllable carriers for improved drug delivery. These liposomes offer enhanced efficacy without causing side effects, showcasing exceptional extracellular stability and controllable intracellular instability. “Our study will contribute towards ensuring healthy lives and promoting well-being for people of all ages, which ties in with one of the Sustainable Development Goal (SDG3) of the United Nations,” concludes an optimistic Prof. Sudo.

Release URL:
https://www.eurekalert.org/news-releases/993940

Reference:
Development of light-induced disruptive liposomes (LiDL) as a photoswitchable carrier for intracellular substance delivery
Journal: Chemical Communications
DOI:10.1039/d3cc02056h

Contact Person:Yuki Sudo
Yuki Sudo is currently affiliated with the Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences at Okayama University in Japan. He received a Ph.D. degree in Pharmaceutical Sciences from Hokkaido University in 2005. He has published 238 research articles, which have been cited around 1,500 times. His research interests include Biophysics, Spectroscopy, Photochemistry, and Chemical Biology. His current research project focuses on the discovery and study of novel retinal proteins in nature. In 2016, he received the Young Scientists’ Prize of the Commendation for Science and Technology by the Minister of Education, Culture, Sports, Science and Technology.