Active particles induce large shape deformations in giant lipid vesicles.
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
04
11
2019
accepted:
24
07
2020
entrez:
1
10
2020
pubmed:
2
10
2020
medline:
12
1
2021
Statut:
ppublish
Résumé
Biological cells generate intricate structures by sculpting their membrane from within to actively sense and respond to external stimuli or to explore their environment
Identifiants
pubmed: 32999485
doi: 10.1038/s41586-020-2730-x
pii: 10.1038/s41586-020-2730-x
doi:
Substances chimiques
Lipid Bilayers
0
Phosphatidylcholines
0
Unilamellar Liposomes
0
1,2-oleoylphosphatidylcholine
EDS2L3ODLV
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
52-56Références
Mattila, P. K. & Lappalainen, P. Filopodia: molecular architecture and cellular functions. Nat. Rev. Mol. Cell Biol. 9, 446–454 (2008).
doi: 10.1038/nrm2406
Fletcher, D. A. & Mullins, R. D. Cell mechanics and the cytoskeleton. Nature 463, 485–492 (2010).
doi: 10.1038/nature08908
Needleman, D. & Dogic, Z. Active matter at the interface between materials science and cell biology. Nat. Rev. Mater. 2, 17048 (2017).
doi: 10.1038/natrevmats.2017.48
Turlier, H. et al. Equilibrium physics breakdown reveals the active nature of red blood cell flickering. Nat. Phys. 12, 513–519 (2016).
doi: 10.1038/nphys3621
Pizarro-Cerdá, J., Charbit, A., Enninga, J., Lafont, F. & Cossart, P. in Seminars in Cell & Developmental Biology Vol. 60, 155–167 (Elsevier, 2016).
Dimova, R. & Marques, C. The Giant Vesicle Book (CRC Press, 2019).
Keber, F. C. et al. Topology and dynamics of active nematic vesicles. Science 345, 1135–1139 (2014).
doi: 10.1126/science.1254784
Mulla, Y., Aufderhorst-Roberts, A. & Koenderink, G. H. Shaping up synthetic cells. Phys. Biol. 15, 041001 (2018).
doi: 10.1088/1478-3975/aab923
Steinkühler, J. et al. Controlled division of cell-sized vesicles by low densities of membrane-bound proteins. Nat. Commun. 11, 905 (2020).
doi: 10.1038/s41467-020-14696-0
Ganzinger, K. A. & Schwille, P. More from less—bottom-up reconstitution of cell biology. J. Cell Sci. 132, 227488 (2019).
doi: 10.1242/jcs.227488
Mellouli, S. et al. Self-organization of the bacterial cell-division protein Ftsz in confined environments. Soft Matter 9, 10493–10500 (2013).
doi: 10.1039/c3sm51163d
Elgeti, J. & Gompper, G. Wall accumulation of self-propelled spheres. Eur. Phys. Lett. 101, 48003 (2013).
doi: 10.1209/0295-5075/101/48003
Fily, Y., Baskaran, A. & Hagan, M. F. Dynamics of self-propelled particles under strong confinement. Soft Matter 10, 5609 (2014).
doi: 10.1039/C4SM00975D
Bechinger, C. et al. Active particles in complex and crowded environments. Rev. Mod. Phys. 88, 045006 (2016).
doi: 10.1103/RevModPhys.88.045006
Gompper, G. et al. The 2019 motile active matter roadmap. J. Phys. Condens. Matter 32, 193001 (2020).
doi: 10.1088/1361-648X/ab6348
Paoluzzi, M., Di Leonardo, R., Marchetti, M. C. & Angelani, L. Shape and displacement fluctuations in soft vesicles filled by active particles. Sci. Rep. 6, 34146 (2016).
doi: 10.1038/srep34146
Wang, C., Guo, Y.-k., Tian, W.-d. & Chen, K. Shape transformation and manipulation of a vesicle by active particles. J. Chem. Phys. 150, 044907 (2019).
doi: 10.1063/1.5078694
Li, Y. & ten Wolde, P. Shape transformations of vesicles induced by swim pressure. Phys. Rev. Lett. 123, 148003 (2019).
doi: 10.1103/PhysRevLett.123.148003
Kroll, D. & Gompper, G. The conformation of fluid membranes: Monte Carlo simulations. Science 255, 968 (1992).
doi: 10.1126/science.1546294
Pécréaux, J., Döbereiner, H.-G., Prost, J., Joanny, J.-F. & Bassereau, P. Refined contour analysis of giant unilamellar vesicles. Eur. Phys. J. E 13, 277–290 (2004).
doi: 10.1140/epje/i2004-10001-9
Heinrich, V. & Waugh, R. E. A piconewton force transducer and its application to measurement of the bending stiffness of phospholipid membranes. Ann. Biomed. Eng. 24, 595–605 (1996).
doi: 10.1007/BF02684228
Cuvelier, D., Derenyi, I., Bassereau, P. & Nassoy, P. Coalescence of membrane tethers: experiments, theory, and applications. Biophys. J. 88, 2714–2726 (2005).
doi: 10.1529/biophysj.104.056473
Takatori, S. C., Yan, W. & Brady, J. F. Swim pressure: stress generation in active matter. Phys. Rev. Lett. 113, 028103 (2014).
doi: 10.1103/PhysRevLett.113.028103
Manneville, J.-B., Bassereau, P., Lévy, D. & Prost, J. Activity of transmembrane proteins induces magnification of shape fluctuations of lipid membranes. Phys. Rev. Lett. 82, 4356–4359 (1999).
doi: 10.1103/PhysRevLett.82.4356
Takatori, S. C. & Sahu, A. Active contact forces drive nonequilibrium fluctuations in membrane vesicles. Phys. Rev. Lett. 124, 158102 (2020).
doi: 10.1103/PhysRevLett.124.158102
Park, Y. et al. Metabolic remodelling of the human red blood cell membrane. Proc. Natl Acad. Sci. USA 107, 1289–1294 (2010).
doi: 10.1073/pnas.0910785107
Natsume, Y. et al. Preparation of giant vesicles encapsulating microspheres by centrifugation of a water-in-oil emulsion. J. Vis. Exp. 119, e55282 (2017).
Song, J.-S., Tronc, F. & Winnik, M. A. Two-stage dispersion polymerization toward monodisperse, controlled micrometre-sized copolymer particles. J. Am. Chem. Soc. 126, 6562–6563 (2004).
doi: 10.1021/ja048862d
Vutukuri, H. R., Bet, B., Van Roij, R., Dijkstra, M. & Huck, W. T. Rational design and dynamics of self-propelled colloidal bead chains: from rotators to flagella. Sci. Rep. 7, 16758 (2017).
doi: 10.1038/s41598-017-16731-5
Drabik, D., Przybyło, M., Chodaczek, G., Iglič, A. & Langner, M. The modified fluorescence based vesicle fluctuation spectroscopy technique for determination of lipid bilayer bending properties. Biochim. Biophys. Acta Biomembr. 1858, 244–252 (2016).
doi: 10.1016/j.bbamem.2015.11.020
Yoon, Y.-Z. et al. Flickering analysis of erythrocyte mechanical properties: dependence on oxygenation level, cell shape, and hydration level. Biophys. J. 97, 1606–1615 (2009).
doi: 10.1016/j.bpj.2009.06.028
Bassereau, P., Sorre, B. & Lévy, A. Bending lipid membranes: experiments after W. Helfrich’s model. Adv. Colloid Interface Sci. 208, 47–57 (2014).
doi: 10.1016/j.cis.2014.02.002
Frigo, M. & Johnson, S. G. The design and implementation of FFTW3. Proc. IEEE 93, 216–231 (2005).
doi: 10.1109/JPROC.2004.840301
Gompper, G. & Kroll, D. M. in Statistical Mechanics of Membranes and Surfaces 2nd edn (eds Nelson, D. R. et al.) 359–426 (World Scientific, 2004).
Noguchi, H. & Gompper, G. Dynamics of fluid vesicles in shear flow: effect of the membrane viscosity and thermal fluctuations. Phys. Rev. E 72, 011901 (2005).
doi: 10.1103/PhysRevE.72.011901
Helfrich, W. Elastic properties of lipid bilayers: theory and possible experiments. Z. Naturforsch. C 28, 693–703 (1973).
doi: 10.1515/znc-1973-11-1209
Gompper, G. & Kroll, D. Random surface discretizations and the renormalization of the bending rigidity. J. Phys. I 6, 1305–1320 (1996).
Gompper, G. & Kroll, D. M. Network models of fluid, hexatic and polymerized membranes. J. Phys. Condens. Matter 9, 8795–8834 (1997).
doi: 10.1088/0953-8984/9/42/001
Guckenberger, A. & Gekle, S. Theory and algorithms to compute Helfrich bending forces: a review. J. Phys. Condens. Matter 29, 203001 (2017).
doi: 10.1088/1361-648X/aa6313
Allen, M. P. & Tildesley, D. J. Computer Simulation of Liquids (Clarendon Press, 1991).
Noguchi, H. & Gompper, G. Fluid vesicles with viscous membranes in shear flow. Phys. Rev. Lett. 93, 258102 (2004).
doi: 10.1103/PhysRevLett.93.258102
Wysocki, A., Winkler, R. G. & Gompper, G. Cooperative motion of active Brownian spheres in three-dimensional dense suspensions. Eur. Phys. Lett. 105, 48004 (2014).
doi: 10.1209/0295-5075/105/48004
Stenhammar, J., Marenduzzo, D., Allen, R. J. & Cates, M. E. Phase behaviour of active Brownian particles: the role of dimensionality. Soft Matter 10, 1489–1499 (2014).
doi: 10.1039/C3SM52813H