Using Simple Fluid Wetting as a Model for Cell Spreading

Similar documents
High Throughput In-Silico Screening Against Flexible Protein Receptors

Modeling the Free Energy of Polypeptides in Different Environments

Hamiltonian Replica Exchange Molecular Dynamics Using Soft-Core Interactions to Enhance Conformational Sampling

Exploring the Free Energy Surface of Short Peptides by Using Metadynamics

Wetting Transitions at Fluid Interfaces and Related Topics

Line adsorption in a mean-field density functional model

Modelling of Possible Binding Modes of Caffeic Acid Derivatives to JAK3 Kinase

Aggregation of the Amyloid-β Protein: Monte Carlo Optimization Study

Jacco Snoeijer PHYSICS OF FLUIDS

THE MODIFIED YOUNG S EQUATION FOR THE CONTACT ANGLE OF A SMALL SESSILE DROP FROM AN INTERFACE DISPLACEMENT MODEL

Scalable Systems for Computational Biology

Molecular Dynamics Simulations of the Metaloenzyme Thiocyanate Hydrolase with Non-Corrinoid Co(III) in Active Site

Conformational Studies of UDP-GlcNAc in Environments of Increasing Complexity

Line and boundary tensions on approach to the wetting transition

Line Tension Effect upon Static Wetting

How much does the core structure of a three-phase contact line contribute to the line tension near a wetting transition?

spreading of drops on soft surfaces

Binary Hard-Sphere Mixtures Within Spherical Pores

Long-time behavior and different shear regimes in quenched binary mixtures

arxiv: v2 [cond-mat.other] 16 Dec 2011

Four-phase merging in sessile compound drops

Capillary Contact Angle in a Completely Wet Groove

Quark Physics from Lattice QCD

Thermodynamic expansion of nucleation free-energy barrier and size of critical nucleus near the vapor-liquid coexistence

COMPARISON OF WETTABILITY AND CAPILLARY EFFECT EVALUATED BY DIFFERENT CHARACTERIZING METHODS

Physics 106a/196a Problem Set 7 Due Dec 2, 2005

Molecular Simulation Study of the Effect of Pressure on the Vapor-Liquid Interface of the Square-Well Fluid

Exercise: concepts from chapter 10

Module17: Intermolecular Force between Surfaces and Particles. Lecture 23: Intermolecular Force between Surfaces and Particles

Effect of interfacial dislocations on ferroelectric phase stability and domain morphology in a thin film a phase-field model

Capillarity and Wetting Phenomena

Exchange Frequencies in 2D Solids: Example of Helium 3 Adsorbed on Graphite and the Wigner Crystal

De novo all atom folding of helical proteins

Continuum Model of Avalanches in Granular Media

Absorption of gas by a falling liquid film

Direct determination of the Tolman length from the bulk pressures of liquid drops via molecular dynamics simulations

Modeling Interfaces in Structural Dynamics Analysis

the expansion for the Helmholtz energy derived in Appendix A, part 2, the expression for the surface tension becomes: σ = ( a + ½ k(ρ) ρ 2 x ) dx

Capillarity. ESS5855 Lecture Fall 2010

Electrical Connections

Molecular dynamics investigation of thickness effect on liquid films

Supporting Information for Conical Nanopores. for Efficient Ion Pumping and Desalination

INTERFACIAL PHENOMENA GRADING SCHEME

arxiv: v1 [physics.class-ph] 13 Sep 2008

The Wilhelmy balance. How can we measure surface tension? Surface tension, contact angles and wettability. Measuring surface tension.

DRIVING FORCE IN SIMULATION OF PHASE TRANSITION FRONT PROPAGATION

Mass Transfer Fundamentals. Chapter#3

Nucleation rate (m -3 s -1 ) Radius of water nano droplet (Å) 1e+00 1e-64 1e-128 1e-192 1e-256

Bulk permittivity of a composite with coated spheroidal filler particles

Entropic wetting and the fluid fluid interface of a model colloid polymer mixture

arxiv: v1 [physics.bio-ph] 26 Nov 2007

Praktikum zur. Materialanalytik

CONTROLLING CHAOS. Sudeshna Sinha. The Institute of Mathematical Sciences Chennai

Creating Localized Mixing Stations within Microfluidic Channels

Free energy concept Free energy approach LBM implementation Parameters

Compression and entanglement, entanglement transformations

Derivation of continuum models for the moving contact line problem based on thermodynamic principles. Abstract

On the displacement of three-dimensional fluid droplets adhering to a plane wall in viscous pressure-driven flows

arxiv:q-bio/ v1 [q-bio.qm] 30 Nov 2003

Generalized continuum theory for ferroelectric thin films

Phenomenological Theories of Nucleation

Theory of Interfacial Tension of Partially Miscible Liquids

arxiv:cond-mat/ v1 [cond-mat.stat-mech] 11 Dec 2002

Invaded cluster dynamics for frustrated models

arxiv: v1 [physics.class-ph] 16 Jan 2008

Size-Selective Nanoparticle Assembly on Substrates. by DNA Density Patterning

Supporting Information for Lysozyme Adsorption in ph-responsive Hydrogel Thin-Films: The non-trivial Role of Acid-Base Equilibrium

VIII. Phase Transformations. Lecture 38: Nucleation and Spinodal Decomposition

The Biot-Savart Law: From Infinitesimal to Infinite

Spri ringer. INTERFACIAL TRANSPORT PHENOMENA 2 nd Edition. John C. Slattery Department ofaerospace Engineering Texas A&M University

Mush liquid interfaces with cross flow

NCHRP FY 2004 Rotational Limits for Elastomeric Bearings. Final Report. Appendix I. John F. Stanton Charles W. Roeder Peter Mackenzie-Helnwein

Generalized Wenzel equation for contact angle of droplets on spherical rough solid substrates

Distance Between Ellipses in 2D

ENAS 606 : Polymer Physics

The thermodynamics of solid-solid interfaces in systems of fixed mass

ISCST shall not be responsible for statements or opinions contained in papers or printed in its publications.

Interface Profiles in Field Theory

PORE-SCALE PHASE FIELD MODEL OF TWO-PHASE FLOW IN POROUS MEDIUM

5.2 Surface Tension Capillary Pressure: The Young-Laplace Equation. Figure 5.1 Origin of surface tension at liquid-vapor interface.

ADSORPTION IN MICROPOROUS MATERIALS: ANALYTICAL EQUATIONS FOR TYPE I ISOTHERMS AT HIGH PRESSURE

Short-Term Scientific Mission (STSM) Report for Nematic-Smectic Pattern Formation in Confined Geometries Action TD

Monte Carlo Simulation of Long-Range Self-Diffusion in Model Porous Membranes and Catalysts

+ S/y. The wetted portion of the surface is then delimited by a certain contact line L (here a

PF BC. When is it Energetically Favourable for a Rivulet of Perfectly Wetting Fluid to Split?

BRIEF COMMUNICATION TO SURFACES ANALYSIS OF ADHESION OF LARGE VESICLES

Application of the variational calculus to wetting phenomena in chemical engineering

Floating Drops. Ray Treinen. January 26, University of Toledo. Ray Treinen (University of Toledo) Floating Drops January 26, / 32

Heat Transfer of Condensation in Smooth Round Tube from Superheated Vapor

Molecular Modeling and Simulation of Phase Equilibria for Chemical Engineering

Electrochemical methods : Fundamentals and Applications

Direct calculation of interfacial tensions from computer simulation: Results for freely jointed tangent hard sphere chains

AIMS Education Foundation

Clusters and Percolation

CHEMICAL ENGINEERING (CHE)

Recapitulation: Questions on Chaps. 1 and 2 #A

KOROSH TORABI. Ph.D. Chemical Engineering, Purdue University, West Lafayette, IN Dec. 2011

Frieder Mugele. Physics of Complex Fluids. University of Twente. Jacco Snoeier Physics of Fluids / UT

Developed and Published by. AIMS Education Foundation

The glass transition as a spin glass problem

Transcription:

John von Neumann Institute for Computing Using Simple Fluid Wetting as a Model for Cell Spreading Matthew Reuter, Caroline Taylor published in NIC Workshop 26, From Computational Biophysics to Systems Biology, Jan Meinke, Olav Zimmermann, Sandipan Mohanty, Ulrich H.E. Hansmann (Editors) John von Neumann Institute for Computing, Jülich, NIC Series, Vol. 34, ISBN-1: 3-981843--6, ISBN-13: 978-3-981843--6, pp. 137-14, 26. c 26 by John von Neumann Institute for Computing Permission to make digital or hard copies of portions of this work for personal or classroom use is granted provided that the copies are not made or distributed for profit or commercial advantage and that copies bear this notice and the full citation on the first page. To copy otherwise requires prior specific permission by the publisher mentioned above. http://www.fz-juelich.de/nic-series/volume34

Using Simple Fluid Wetting as a Model for Cell Spreading Matthew Reuter and Caroline Taylor Department of Chemistry, Michigan Technological University Houghton, Michigan 49931, USA E-mail: cmtaylor@mtu.edu Cell morphology in contact with external media is dictated by the cell s interactions with the external media. One component that influences morphology is the thermodynamic aspect of cell spreading, which can be seen as analogous to wetting in a three-phase equilibrium. Results of classical density functional theory within the mean field approximation for a binary fluid are summarized to motivate simple changes to the model through the effective mass coefficient. We find that by altering the effective interactions we can alter the stable morphology, increasing contact by increasing component similarity. Thus we are able to propose a systematic approach to modeling cell spreading from simple mean field results. 1 Background The spreading of a cell on a surface, though complex, is driven primarily by two components. One is a mechanical force from actin filament formation. The other is a more thermodynamic driving force, associated with balancing surface interactions, that allows analogy to simple wetting phenomena. This influence is visible in cell-cell contacts, such as found in tissues, and is of particular importance in biomedical applications 1, where patterned substrates are often employed in the design of biomimetic materials 2. The rate and extent of adsorption depends on the surface film s composition 3, 4, which is exploited in micro-patterning applications 5. To develop the thermodynamic basis for cellular spreading from a line of three-phase contact, the cell-substrate-surround system can be envisioned as a constrained three-phase equilibrium, where there are two true phases and a third (the cell) which mimics one. Viewed in such a manner, there is readily conceivable an analog to the line tension which behaves characteristically in the spreading process, as is the case for a drop on a surface. There are three general morphologies available to a drop in contact with an interface, shown in Figure 1. These are determined by the balance of interactions between the phases and characterized by a contact angle determined directly via Young s Law 6. The drop can bead (Fig. 1) or spread only minimally (non-wetting), as the system attempts to minimize the unfavorable interactions between the phases. Alternatively, it can spread unrestrictedly across the surface and wet it completely (Fig. 1(c)). Between these two regimes there is an intermediate state, in which the drop only partially wets the surface (Fig. 1). In these instances, there is a line of three-phase contact along the drop boundary. Immediately before complete wetting, there is another possibility, that of pre-wetting (Fig. 1(d)), in which a layer of finite thickness first coats the interface before a discontinuous transition to infinite thickness occurs. Because the extent of cellular spreading is bounded by the cell membrane, it is to this final possibility that comparisons are most natural. current address: Department of Chemistry, Northwestern University, Evanston, IL 628 The author also holds a visiting appointment at the James Franck Institute, University of Chicago, Chicago, Illinois 6637, USA. 137

θ θ (c) (d) Figure 1. Wetting states possible for a drop on a surface: non-wetting; partial wetting; (c) complete wetting; (d) pre-wetting. 2 Simple Fluid wetting in a binary system A binary three-phase system consists of two components (i = 1, 2) in three phases (,, ), all of which are in equilibrium with each other, as shown in Figure 2, and is described by a free energy functional dependent upon the spatial component densities, F [, ]. At the intersection of the three two-phase boundaries (I =,, ), there is a line where all three phases are in contact. About this boundary there is a two-dimensional region of inhomogeneities which gives rise to an excess concentration along the line of three-phase contact. This results in an excess contribution to the free energy, yielding the line tension. A commonly assumed model free energy density, Ψ, accounts for the variation of the densities in the region of the phase interfaces to second order: Ψ = F [, ] + 1 m ij ρ i ρ j, (1) 2 where m ij is a constant mass interaction term. The surface tension, σ I, is determined by integrating this excess across the interface. The overall excess free energy is found similarly, and the surface excesses subtracted to yield the line tension: [ τ = min Ψ[, ]da ] (σ I R I ) = (Ψ[, ] 2F[, ])da. (2) ρ A I A The latter form of the line tension, due to Kerins and Boiteux 7, converges to the preceding variational form. Solving the Euler-Lagrange equations subject to the bulk conditions is i,j = b θ θ θ = +1 = 1 (c) Figure 2. Model system for a drop of phase at the interface between phases and. : Top view of the drop showing the three-phase contact (dashed line); : Side view of the drop on the interface; (c): Region normal to the line of three-phase contact, showing the bulk component densities in each of the phases. 138

τ 1.4 1.2 1.8.6.4.2 -.2 -.4 -.6 contact angle, θ 2 4 6 8 1 12 vs. θ vs. b 2 ln(τ w τ) 1-1 -2-3 -4-5 -14-12 -1-8 -6-4 -2 ln(b-b w ).5 1 1.5 2 2.5 3 b 2 ξ rel 12 ξ 1 8 ξ 6 4 ξ A rel 12 1 8 6 4 2 2 4 6 8 1 12 2 2 4 6 8 1 12 contact angle, θ Figure 3. Results of solving the model binary system. Line tension approaching wetting; Response of the contact regions approaching the transition, relative to the b = 3 values. Used by permission from Ref. 9. equivalent to minimizing the the free energy per unit area and yields the equilibrium density profiles without restricting them to a particular form. The model system studied previously by Taylor and Widom 8, 9 is shown in Figure 2(c). It is described by a model free energy functional, F [, ; b] 1, which depends upon the relative component densities and a parameter (b, the bulk density of one of the components) which can be varied to induce a wetting transition, and m ij = δ ij. The line tension and contact region in this model exhibit an interesting behavior approaching the wetting transition, both changing qualitatively at the same point. In the line tension, shown in Figure 3, the slope changes near 2. A shift between clearly different structures occurs in the that region (b 2.3, θ 2 ), resulting in an average behavior which satisfies the mean field prediction. The spatial extent of the inhomogeneous region of the phase contact (measured by the correlation length ξ), Figure 3, supports this, exhibiting a distinct plateau in the growth rate of the contact area at the same region. Thus in even a so simple model there is non-uniformity, and it is this observation which motivates our current work, as it facilitates extension to systems where such behavior is involved. Such an approach allows the model to be applied to more complex systems by incorporating simple modifications. 3 Extending the model The simple picture above is modified by altering the balance of the components within the square-gradient approximation, by scaling the off-diagonal values of the effective mass interaction parameter, m ij. The rest of the model is as in the work of Taylor and Widom 9. A first test employs a value of m 12.75 and maintains the self-interaction constant at unity. In this manner, the components are made to appear more similar, and the static contact angle (b = 3, m 12.75) is 114, showing a greater extent of spreading (b = 3, m12 gives 12 ). This suggests that the variable morphology can be described by such a change in the simple model, although whether a wetting transition can be induced by such an external parameter is still undetermined. From the phenomenological first steps, the mass interaction coefficient must be related 139

to physically-relevant values. The obvious way to do so is to establish a reference state chosen based on the problem, and relate m ij to it, m ij = 1 ǫ i ǫ j ǫ. In addition, an i +ǫ j alternative form of the free energy functional itself is being constructed, with additional components that more closely mimic the real system 11. 4 Concluding Remarks The use of a simple wetting model is not uncommon as an initial extension in studies of cell spreading, and it is promising that altering the effective component interactions does alter the morphology. The benefit of this model is that it is relatively tractable, while maintaining many of the characteristics of the unmanageably complex real system, and is readily extensible to higher levels of complexity (i.e. made more physical). It is thus fruitful to consider the system on as simple a level as possible, and incorporate higher levels of complexity systematically. Within this classical wetting framework, a cell spreading on a surface can be represented as a set of three two-phase interfaces and simulations of slabs containing these interfaces used to determine the interfacial tensions (from the pressure tensor). From these, the analogues to the contact angle and line tension can be calculated via the spreading coefficient. Thus we may also carry out simple simulations that test the added complexity in the model and guide its development. Acknowledgments Funding for this work is provided by the Research Excellence Fund of the State of Michigan and Michigan Technological University. We are grateful to Benjamin Widom, Walter Nadler, and Prabhakar Bhimalapuram for many helpful and illuminating discussions. References 1. D. Falconnet, G. Csucs, H. M. Grandin, and M. Textor. Biomat., 27:344 363,26. 2. M. N. De Silva, J. Paulsen, M. J. Renn, and D. J. Odde. Biotech. Bioeng., 93:919 927, 26. 3. Y. Kikkawa, M. Fujita, T. Hiraishi, M. Yoshimoto, and Y. Doi. Biomacromolecules, 5:1642 1646, 24. 4. B. Nguyen, A. Upadhyaya, A. van Oudenaarden, and M. P. Brenner. Biophys. J., 86:274 2474, 24. 5. D. Lehnert, B. Wehrie-Haller, C. David, U. Weiland, and C. Ballestrem. J. Cell Sci., 117:41 52, 23. 6. J. S. Rowlinson and B. Widom. Molecular theory of capillarity. Clarendon Press, Oxford, 1982. 7. J. Kerins and M. Boiteux. Physica A, 117:575 592, 1983. 8. C. M. Taylor and B. Widom. Mol. Phys., 13:647 655, 25. 9. C. M. Taylor and B. Widom. Phys. A, 358:492 54, 25. 1. I. Szleifer and B. Widom. Mol. Phys., 75:925 943, 1992. 11. M. Reuter and C. M. Taylor. work in progress, 26. 14