Rhythmic pore dynamics in a shrinking lipid vesicle

Physical Review E - Statistical, Nonlinear, and Soft Matter Physics

Volumn 80, Issue 5, 2009, Pages

  Hamada, Tsutomu ^a   Hirabayashi, Yuichi ^a   Ohta, Takao ^b   Takagi, Masahiro ^a  

^a JAPAN ADVANCED INSTITUTE OF SCIENCE AND TECHNOLOGY   (Japan)

^b KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CONCENTRATION OF; CYCLE OSCILLATIONS; ELASTIC FREE ENERGY; HIGH CONCENTRATION; LIPID VESICLES; LOW CONCENTRATIONS; MEMBRANE PORES; NONEQUILIBRIUM CONDITIONS; RHYTHMIC MOTION; SURFACTANT TRITON-X; VESICLE SIZE;

DYNAMICS; SHRINKAGE; SURFACE ACTIVE AGENTS;

CONCENTRATION (PROCESS);

EID: 71849108719     PISSN: 15393755     EISSN: 15502376     Source Type: Journal    
DOI: 10.1103/PhysRevE.80.051921     Document Type: Article

References (53)

1. R. Lipowsky and E. Sackmann, Structure and Dynamics of Membranes (Elsevier, New York, 1995).
2. P. L. Luisi and P. Walde, Giant Vesicles (Wiley & Sons, New York, 2000).
3. H.-G. Döbereiner, Curr. Opin. Colloid Interface Sci. 5, 256 (2000). 10.1016/S1359-0294(00)00064-9
4. R. Dimova, S. Aranda, N. Bezlyepkina, V. Nikolov, K. A. Riske, and R. Lipowsky, J. Phys.: Condens. Matter 18, S1151 (2006). 10.1088/0953-8984/18/28/ S04
5. A. Karlsson, R. Karlsson, M. Karsson, A.-S. Cans, A. Strömberg, F. Ryttsén, and O. Orwar, Nature (London) 409, 150 (2001). 10.1038/35051656
6. I. Tsafrir, Y. Caspi, M.-A. Guedeau-Boudeville, T. Arzi, and J. Stavans, Phys. Rev. Lett. 91, 138102 (2003). 10.1103/PhysRevLett.91.138102
7. R. Bar-Ziv, E. Moses, and P. Nelson, Biophys. J. 75, 294 (1998). 10.1016/S0006-3495(98)77515-0
8. T. Baumgart, S. T. Hess, and W. W. Webb, Nature (London) 425, 821 (2003). 10.1038/nature02013
9. T. Hamada, Y. Miura, K. Ishii, S. Araki, K. Yoshikawa, M. Vestergaard, and M. Takagi, J. Phys. Chem. B 111, 10853 (2007). 10.1021/jp075412+
10. N. Khalifat, N. Puff, S. Bonneau, J.-B. Fournier, and M. I. Angelova, Biophys. J. 95, 4924 (2008). 10.1529/biophysj.108.136077
11. S. L. Veatch and S. L. Keller, Biochim. Biophys. Acta 1746, 172 (2005). 10.1016/j.bbamcr.2005.06.010
12. E. Evans, V. Heinrich, F. Ludwig, and W. Rawicz, Biophys. J. 85, 2342 (2003). 10.1016/S0006-3495(03)74658-X
13. M. Yanagisawa, M. Imai, and T. Taniguchi, Phys. Rev. Lett. 100, 148102 (2008). 10.1103/PhysRevLett.100.148102
14. U. Seifert, K. Berndl, and R. Lipowsky, Phys. Rev. A 44, 1182 (1991). 10.1103/PhysRevA.44.1182
15. L. Miao, U. Seifert, M. Wortis, and H.-G. Döbereiner, Phys. Rev. E 49, 5389 (1994). 10.1103/PhysRevE.49.5389
16. U. Seifert, Adv. Phys. 46, 13 (1997). 10.1080/00018739700101488
17. P. Ziherl and S. Svetina, Europhys. Lett. 70, 690 (2005). 10.1209/epl/i2004-10527-4
18. G. Lim H. W., M. Wortis, and R. Mukhopadhyay, Proc. Natl. Acad. Sci. U.S.A. 99, 16766 (2002). 10.1073/pnas.202617299
19. L. Bagatolli and P. B. S. Kumar, Soft Matter 5, 3234 (2009). 10.1039/b901866b
20. J. Käs and E. Sackmann, Biophys. J. 60, 825 (1991). 10.1016/S0006-3495(91)82117-8
21. K. Ishii, T. Hamada, M. Hatakeyama, R. Sugimoto, T. Nagasaki, and M. Takagi, ChemBioChem 10, 251 (2009). 10.1002/cbic.200800482
22. S. Ramaswamy and M. Rao, C. R. Acad. Sci., Ser. IV Phys. Astrophys. 2, 817 (2001).
23. F. Nomura, M. Nagata, T. Inaba, H. Hiramatsu, H. Hotani, and K. Takiguchi, Proc. Natl. Acad. Sci. U.S.A. 98, 2340 (2001). 10.1073/pnas.041419098
24. O. Sandre, L. Moreaux, and F. Brochard-Wyart, Proc. Natl. Acad. Sci. U.S.A. 96, 10591 (1999). 10.1073/pnas.96.19.10591
25. F. Brochard-Wyart, P. G. de Gennes, and O. Sandre, Physica A 278, 32 (2000). 10.1016/S0378-4371(99)00559-2
26. E. Karatekin, O. Sandre, H. Guitouni, N. Borghi, P.-H. Puech, and F. Brochard-Wyart, Biophys. J. 84, 1734 (2003). 10.1016/S0006-3495(03)74981-9
27. E. Karatekin, O. Sandre, and F. Brochard-Wyart, Polym. Int. 52, 486 (2003). 10.1002/pi.1007
28. J. Prost and R. Bruinsma, Europhys. Lett. 33, 321 (1996). 10.1209/epl/i1996-00340-1
29. J.-B. Manneville, P. Bassereau, S. Ramaswamy, and J. Prost, Phys. Rev. E 64, 021908 (2001). 10.1103/PhysRevE.64.021908
30. P. Girard, J. Prost, and P. Bassereau, Phys. Rev. Lett. 94, 088102 (2005). 10.1103/PhysRevLett.94.088102
31. M. D. El Alaoui Faris, D. Lacoste, J. Pécréaux, J.-F. Joanny, J. Prost, and P. Bassereau, Phys. Rev. Lett. 102, 038102 (2009). 10.1103/PhysRevLett.102.038102
32. K. H. de Haas, C. Blom, D. van den Ende, M. H. G. Duits, and J. Mellema, Phys. Rev. E 56, 7132 (1997). 10.1103/PhysRevE.56.7132
33. M.-A. Mader, V. Vitkova, M. Abkarian, A. Viallat, and T. Podgorski, Eur. Phys. J. E 19, 389 (2006). 10.1140/epje/i2005-10058-x
34. J. Deschamps, V. Kantsler, and V. Steinberg, Phys. Rev. Lett. 102, 118105 (2009). 10.1103/PhysRevLett.102.118105
35. J. Beaucourt, F. Rioual, T. Séon, T. Biben, and C. Misbah, Phys. Rev. E 69, 011906 (2004). 10.1103/PhysRevE.69.011906
36. H. Noguchi and G. Gompper, Phys. Rev. Lett. 98, 128103 (2007). 10.1103/PhysRevLett.98.128103
37. U. Seifert, Eur. Phys. J. B 8, 405 (1999). 10.1007/s100510050706
38. P. M. Vlahovska and R. S. Gracia, Phys. Rev. E 75, 016313 (2007). 10.1103/PhysRevE.75.016313
39. V. V. Lebedev, K. S. Turitsyn, and S. S. Vergeles, Phys. Rev. Lett. 99, 218101 (2007). 10.1103/PhysRevLett.99.218101
40. R. Finken, A. Lamura, U. Seifert, and G. Gompper, Eur. Phys. J. E 25, 309 (2008). 10.1140/epje/i2007-10299-7
41. M. Almgren, Biochim. Biophys. Acta 1508, 146 (2000). 10.1016/S0005- 2736(00)00309-6
42. M.-T. Paternostre, M. Roux, and J.-L. Rigaud, Biochemistry 27, 2668 (1988). 10.1021/bi00408a006
43. A. de la Maza and J. L. Parra, Langmuir 11, 2435 (1995). 10.1021/la00007a021
44. U. Kragh-Hansen, M. le Maire, and J. V. Møller, Biophys. J. 75, 2932 (1998). 10.1016/S0006-3495(98)77735-5
45. K.-C. Huang, C.-M. Lin, H.-K. Tsao, and Y.-J. Sheng, J. Chem. Phys. 130, 245101 (2009). 10.1063/1.3155209
46. T. Umeda, F. Nomura, T. Inaba, K. Takiguchi, and H. Hotani, ChemPhysChem 6, 1047 (2005). 10.1002/cphc.200400519
47. M. Kaga and T. Ohta, Eur. Phys. J. E 21, 91 (2006). 10.1140/epje/i2006- 10050-0
48. M. Kaga and T. Ohta, J. Phys. Soc. Jpn. 76, 094003 (2007). 10.1143/JPSJ.76.094003
49. K. Tsumoto, H. Matsuo, M. Tomita, and T. Yoshimura, Colloids Surf., B 68, 98 (2009). 10.1016/j.colsurfb.2008.09.023
50. See EPAPS Document No. E-PLEEE8-80-119911 for movies of rhythmic-pore shrinkage (movie1.mpeg) and continuous-pore shrinkage (movie2.mpg). The movies shown are in real speed. For more information on EPAPS, see http://www.aip.org/ pubservs/epaps.html.
51. We adjusted the microscopic focus position to the vesicle equator and preferentially detected pores opened at the vesicle equator for the images and movies. In addition to the pores, enhanced membrane thermal fluctuation is observed within the pore-opening vesicles due to the temporary gain of excess area. Even if a pore appears on the pole of vesicles far from the microscopic focus position, we can decide when vesicles open a pore according to the observed membrane fluctuation behavior. Thus, our analyses such as cycle period are not affected by the out-of-focus position of opening pores.
52. We consider that the loss of membrane materials from the inner and outer leaflets of the bilayer is essentially simultaneous. It is because that surfactant-saturated fluid membranes show rapid flip-flop and materials are quickly distributed between the leaflets, see M. le Maire, J. V. Møller, and P. Champeil, Biochemistry 26, 4803 (1987). 10.1021/bi00389a030
53. We previously reported the dynamic response of phase-separated giant vesicles upon the addition of TX-100 in Ref.. The increase in membrane area induced budding of the phase domains due to the line energy of phase boundaries, while the homogeneous vesicles studied here show large deformations of the entire membrane surface.