Forming giant vesicles with controlled membrane composition, asymmetry, and contents
Models, Molecular
Phosphatidylinositol 4,5-Diphosphate
0301 basic medicine
Microscopy, Confocal
Qa-SNARE Proteins
Rhodamines
106002 Biochemie
Green Fluorescent Proteins
Microfluidics
Membrane Proteins
106002 Biochemistry
Biological Transport
Rats
R-SNARE Proteins
Kinetics
Membrane Lipids
03 medical and health sciences
Models, Chemical
Phosphatidylcholines
Animals
SNARE Proteins
Porosity
Unilamellar Liposomes
Protein Binding
DOI:
10.1073/pnas.1016410108
Publication Date:
2011-05-19T04:44:34Z
AUTHORS (6)
ABSTRACT
Growing knowledge of the key molecular components involved in biological processes such as endocytosis, exocytosis, and motility has enabled direct testing of proposed mechanistic models by reconstitution. However, current techniques for building increasingly complex cellular structures and functions from purified components are limited in their ability to create conditions that emulate the physical and biochemical constraints of real cells. Here we present an integrated method for forming giant unilamellar vesicles with simultaneous control over (i) lipid composition and asymmetry, (ii) oriented membrane protein incorporation, and (iii) internal contents. As an application of this method, we constructed a synthetic system in which membrane proteins were delivered to the outside of giant vesicles, mimicking aspects of exocytosis. Using confocal fluorescence microscopy, we visualized small encapsulated vesicles docking and mixing membrane components with the giant vesicle membrane, resulting in exposure of previously encapsulated membrane proteins to the external environment. This method for creating giant vesicles can be used to test models of biological processes that depend on confined volume and complex membrane composition, and it may be useful in constructing functional systems for therapeutic and biomaterials applications.
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