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Making artificial cells like soap bubbles!

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Posted August 4, 2016
This news or article is intended for readers with certain scientific or professional knowledge in the field.

Researchers at the University of Tokyo used MEMS (Micro Electro Mechanical Systems) technology to produce spherical vesicles (asymmetric giant lipid vesicles/liposomes) surrounded by a membrane that, like the membrane of our cells, has an inner and outer layer composed of different phospholipids. In contrast to conventional methods of creating vesicles, this new method leaves little trace of organic solvents inside the vesicle and is an important contribution as a fundamental technique for development of artificial cell models.

A cross-sectional view of an asymmetric GV that mimics a cell membrane The lipid flip-flop behavior and the improvement of the reconstitution ratio of the membrane proteins. This will be a useful tool for researching the mysteries of asymmetric cell membranes. Image credit: Aki Sato.

A cross-sectional view of an asymmetric GV that mimics a cell membrane. The lipid flip-flop behavior and the improvement of the reconstitution ratio of the membrane proteins. This will be a useful tool for researching the mysteries of asymmetric cell membranes. Image credit: Aki Sato.

Giant liposome formation methods using MEMS technology can better control the size and the encapsulated concentration compared with conventional formation methods. However, when using these formation methods based on the MEMS technology, it is impossible to avoid incorporating organic solvents in the liposome membranes, greatly affecting the stability of the liposome and rendering such methods unsuitable as a tool for researching artificial cells.

Professor Shoji Takeuchi at the Institute of Industrial Science, the University of Tokyo, and Researcher Koki Kamiya at the Kanagawa Academy of Science and Technology and their colleagues have successfully produced asymmetric giant lipid vesicles (GVs) that include little organic solvent by using MEMS technology, applying a water jet to a phospholipid planar bilayer membrane in a manner similar to the creation of a soap bubble. Lipids in the asymmetric GVs were observed flipping between the inner and outer layers of the membrane at approximately the same timescale as cell death occurs in living cells. In addition, when the group added peptides (protein fragments) that interact with lipid membranes, the flip-flop activity was promoted approximately tenfold compared to normal conditions. Moreover, they revealed an increase in uptake of membrane proteins when the outer layer of the asymmetric GVs contains negatively charged lipids.

Using our asymmetric GVs, we observed the dynamics of lipid molecules and the reconstitution of membrane proteins into the asymmetric lipid bilayer,” says Takeuchi. He continues, “Our asymmetric GVs provide a platform to understand the biological functions of lipid asymmetry.”

This research was carried out in collaboration with Kanagawa Academy of Science and Technology and Kyoto University and is now available in the journal Nature Chemistry.

Source: University of Tokyo

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