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Originally published as Biophys J. BioFAST on February 9, 2007.
doi:10.1529/biophysj.106.097105
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Biophysical Journal 92:3178-3194 (2007)
© 2007 The Biophysical Society

Single GUV Method Reveals Interaction of Tea Catechin (–)-Epigallocatechin Gallate with Lipid Membranes

Yukihiro Tamba *, Shinya Ohba {dagger}, Masayo Kubota {ddagger}, Hiroe Yoshioka {ddagger}, Hisashi Yoshioka ¶ and Masahito Yamazaki * {dagger} §

* Innovative Joint Research Center, Shizuoka University, Hamamatsu 432-8011, Japan; {dagger} Department of Physics, Faculty of Science, {ddagger} Radiochemical Research Laboratory, Faculty of Science, and § Integrated Bioscience Section, Graduate School of Science and Technology, Shizuoka University, Shizuoka 422-8529, Japan; and Institute for Environmental Sciences, Shizuoka University, Shizuoka 422-8526, Japan

Correspondence: Address reprint requests to Dr. Masahito Yamazaki, Integrated Bioscience Section, Graduate School of Science and Technology, Shizuoka University, 836 Oya, Suruga-ku, Shizuoka 422-8529, Japan. Tel./Fax: 81-54-238-4741; E-mail: spmyama{at}ipc.shizuoka.ac.jp.

Tea catechins, which are flavonoids and the main components of green tea extracts, are thought to have antibacterial and antioxidant activity. Several studies indicate that lipid membranes are one of the targets of the antibacterial activity of catechins. Studies using a suspension of large unilamellar vesicles (LUVs) indicate that catechin causes gradual leakage of internal contents from LUVs. However, the detailed characteristics of the interaction of catechins with lipid membranes remain unclear. In this study, we investigated the interaction of (–)-epigallocatechin gallate (EGCg), a major catechin in tea extract, with single giant unilamellar vesicles (GUVs) of egg phosphatidylcholine (egg PC) using phase-contrast fluorescence microscopy and the single GUV method. We prepared GUVs of lipid membranes of egg PC in a physiological ion concentration (~150 mM NaCl) using the polyethylene glycol-lipid method. Low concentrations of EGCg at and above 30 µM induced rapid leakage of a fluorescent probe, calcein, from the inside of single egg PC-GUVs; after the leakage, the GUVs changed into small lumps of lipid membranes. On the other hand, phase-contrast microscopic images revealed the detailed process of the EGCg-induced burst of GUVs, the decrease in their diameter, and their transformation into small lumps. The dependence of the fraction of burst GUVs on EGCg concentration was almost the same as that of the fraction of leaked GUV. This correlation strongly indicates that the leakage of calcein from the inside to the outside of the GUV occurred as a result of the burst of the GUV. The fraction of completely leaked GUV and the fraction of the burst GUV increased with time and also increased with increasing EGCg concentration. We compared the EGCg-induced leakage from single GUVs with EGCg-induced leakage from a LUV suspension. The analysis of the EGCg-induced shape changes shows that the binding of EGCg to the external monolayer of the GUV increases its membrane area, inducing an increase in its surface pressure. Small angle x-ray scattering experiments indicate that the intermembrane distance of multilamellar vesicles of PC membrane greatly decreased at EGCg concentrations above the threshold, suggesting that neighboring membranes came in close contact with each other. On the basis of these results, we discuss the mechanism of the EGCg-induced bursting of vesicles.




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