Computational Analysis of a Cross-linked Actin-like Network
Gels formed from G-actin or other filament-forming monomers exhibit a range of morphologies that differ widely in terms of pore size, fiber diameter, degree of isotropy, and frequency of cross-linking or branching. These characteristics are determined, in large part, by the nature and concentration...
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Published in | Experimental mechanics Vol. 49; no. 1; pp. 91 - 104 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Springer US
01.02.2009
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Abstract | Gels formed from G-actin or other filament-forming monomers exhibit a range of morphologies that differ widely in terms of pore size, fiber diameter, degree of isotropy, and frequency of cross-linking or branching. These characteristics are determined, in large part, by the nature and concentration of the proteins that form cross-links between single filaments, yet little is known how filament-forming monomers and cross-linkers assemble to generate a particular network morphology. Some of the important attributes of a cross-linker are the spatial and angular orientation of its two filament binding sites, its size, and stiffness to both rotation and extension. Here, we introduce a Brownian dynamics (BD) simulation model in three dimensions in which actin monomers polymerize and become cross-linked by two types of cross-linking molecules that form either parallel filament bundles or perpendicular cross-links. We analyze the effects of various system parameters on the growth and morphology of the resulting network. Some scaling behaviors emerge that are insensitive to the detailed choice of parameters. Our model thus has the potential as a base BD model that can be further refined for investigating various actin-related phenomena. |
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AbstractList | Gels formed from G-actin or other filament-forming monomers exhibit a range of morphologies that differ widely in terms of pore size, fiber diameter, degree of isotropy, and frequency of cross-linking or branching. These characteristics are determined, in large part, by the nature and concentration of the proteins that form cross-links between single filaments, yet little is known how filament-forming monomers and cross-linkers assemble to generate a particular network morphology. Some of the important attributes of a cross-linker are the spatial and angular orientation of its two filament binding sites, its size, and stiffness to both rotation and extension. Here, we introduce a Brownian dynamics (BD) simulation model in three dimensions in which actin monomers polymerize and become cross-linked by two types of cross-linking molecules that form either parallel filament bundles or perpendicular cross-links. We analyze the effects of various system parameters on the growth and morphology of the resulting network. Some scaling behaviors emerge that are insensitive to the detailed choice of parameters. Our model thus has the potential as a base BD model that can be further refined for investigating various actin-related phenomena. |
Author | Kim, T. Kamm, R. D. Hwang, W. |
Author_xml | – sequence: 1 givenname: T. surname: Kim fullname: Kim, T. organization: Department of Mechanical Engineering, Massachusetts Institute of Technology – sequence: 2 givenname: W. surname: Hwang fullname: Hwang, W. organization: Department of Biomedical Engineering, Texas A&M University – sequence: 3 givenname: R. D. surname: Kamm fullname: Kamm, R. D. email: rdkamm@mit.edu organization: Departments of Mechanical Engineering and Biological Engineering, Massachusetts Institute of Technology |
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Cites_doi | 10.1083/jcb.153.5.947 10.1021/bi00278a021 10.1074/jbc.270.19.11437 10.1152/japplphysiol.01226.2004 10.1529/biophysj.105.071480 10.1006/jmbi.1999.3332 10.1038/nmat1718 10.1016/S0006-3495(98)77712-4 10.1083/jcb.120.4.923 10.1016/0263-7855(96)00018-5 10.1126/science.347575 10.1103/RevModPhys.66.381 10.1083/jcb.103.6.2747 10.1529/biophysj.105.069765 10.1073/pnas.93.23.12937 10.1103/PhysRevLett.98.168103 10.1021/ma025995f 10.1111/j.1432-1033.1983.tb07160.x 10.1021/ma946418x 10.1529/biophysj.105.073924 10.1103/PhysRevLett.91.108102 10.1242/jcs.100.1.187 10.1016/S0006-3495(01)75731-1 10.1016/S0006-3495(95)79975-1 10.1002/cm.10056 10.1242/jcs.108.6.2131 10.1073/pnas.0510190103 10.1073/pnas.0503732102 10.1103/PhysRevE.68.061907 10.1017/CBO9780511607318 10.1529/biophysj.105.076968 10.1529/biophysj.104.047373 10.1529/biophysj.105.062224 10.1006/jmbi.1996.0571 10.1038/nature05824 10.1093/oso/9780198599579.001.0001 10.1038/347044a0 10.1038/nphys567 10.1074/jbc.M306090200 10.1016/S0006-3495(03)74773-0 10.1016/j.jnnfm.2003.10.006 10.1063/1.1528912 10.1073/pnas.91.26.12962 |
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References | LiaoQDobryninAVRubinsteinMMolecular dynamics simulations of polyelectrolyte solutions: Nonuniform stretching of chains and scaling behaviorMacromolecules20033693386339810.1021/ma025995f BelagyiJGrofPRotational motion of actin monomer at low and high salt concentrationEur J Biochem1983130235335810.1111/j.1432-1033.1983.tb07160.x ClaessensMMAEActin-binding proteins sensitively mediate F-actin bundle stiffnessNat Mater20065974875310.1038/nmat1718 SeptDMcCammonJAThermodynamics and kinetics of actin filament nucleationBiophys J200181266767410.1016/S0006-3495(01)75731-1 TsudaYTorsional rigidity of single actin filaments and actin–actin bond breaking force under torsion measured directly by in vitro micromanipulationP Natl Acad Sci USA19969323129371294210.1073/pnas.93.23.12937 WagnerBCytoskeletal polymer networks: The molecular structure of cross-linkers determines macroscopic propertiesP Natl Acad Sci USA200610338139741397810.1073/pnas.0510190103 OdaTEffect of the length and effective diameter of F-actin on the filament orientation in liquid crystalline sols measured by X-ray fiber diffractionBiophys J19987562672268110.1016/S0006-3495(98)77712-41678786 PenderNMccullochCAGQuantitation of actin polymerization in 2 human fibroblast subtypes responding to mechanical stretchingJ Cell Sci1991100187193 ForgacsGOn the possible role of cytoskeletal filamentous networks in intracellular signaling—an approach based on percolationJ Cell Sci199510821312143 ChuJWVothGAAllostery of actin filaments: Molecular dynamics simulations and coarse-grained analysisP Natl Acad Sci USA200510237131111311610.1073/pnas.0503732102 YuXPCarlssonAEMultiscale study of counterion-induced attraction and bundle formation of F-actin using an ising-like mean-field modelBiophys J20038563532354310.1016/S0006-3495(03)74773-0 KreisTValeRGuidebook to the cytoskeletal and motor proteins19992New York, NYOxford University Press ReifFFundamentals of statistical and thermal physics1965New York, NYMcGraw-Hill PollardTDRate constants for the reactions of Atp–actin and Adp–actin with the ends of actin-filamentsJ Cell Biol198610362747275410.1083/jcb.103.6.2747 MofradMRKKammRDCytoskeletal Mechanics2006New York, NYCambridge University Press GittesFFlexural rigidity of microtubules and actin-filaments measured from thermal fluctuations in shapeJ Cell Biol1993120492393410.1083/jcb.120.4.923 BellGIModels for specific adhesion of cells to cellsScience1978200434261862710.1126/science.347575 HolmesKCAtomic model of the actin filamentNature19903476288444910.1038/347044a0 VolkmannNAn atomic model of actin filaments cross-linked by fimbrin and its implications for bundle assembly and functionJ Cell Biol2001153594795610.1083/jcb.153.5.947 YapBKammRDMechanical deformation of neutrophils into narrow channels induces pseudopod projection and changes in biomechanical propertiesJ Appl Physiol20059851930193910.1152/japplphysiol.01226.2004 IsambertHMaggsACDynamics and rheology of actin solutionsMacromolecules19962931036104010.1021/ma946418x ShlomovitzRGovNSMembrane waves driven by actin and myosinPhys Rev Lett2007981616810316830010.1103/PhysRevLett.98.168103 LeYSeptDCarlssonAEEnergetics and dynamics of constrained actin filament bundlingBiophys J200690124295430410.1529/biophysj.105.076968 AtilganEWirtzDSunSXMechanics and dynamics of actin-driven thin membrane protrusionsBiophys J2006901657610.1529/biophysj.105.071480 CostaKDHuckerWJYinFCPBuckling of actin stress fibers: A new wrinkle in the cytoskeletal tapestryCell Motil Cytoskel200252426627410.1002/cm.10056 DhontJKGBrielsWJInhomogeneous suspensions of rigid rods in flowJ Chem Phys200311831466147810.1063/1.1528912 CooperJAKinetic evidence for a monomer activation step in actin polymerizationBiochemistry19832292193220210.1021/bi00278a021 TrepatXUniversal physical responses to stretch in the living cellNature20074477144592595 HeadDALevineAJMacKintoshECDeformation of cross-linked semiflexible polymer networksPhys Rev Lett20039110108102108102 HiguchiHYanagidaTGoldmanYECompliance of thin-filaments in skinned fibers of rabbit skeletal-muscleBiophys J19956931000101010.1016/S0006-3495(95)79975-1 SeptDElcockAHMcCammonJAComputer simulations of actin polymerization can explain the barbed-pointed end asymmetryJ Mol Biol199929451181118910.1006/jmbi.1999.3332 YasudaRMiyataHKinositaKDirect measurement of the torsional rigidity of single actin filamentsJ Mol Biol1996263222723610.1006/jmbi.1996.0571 HumphreyWDalkeASchultenKVMD: Visual molecular dynamicsJ Mol Graph1996141333810.1016/0263-7855(96)00018-5 UnderhillPTDoylePSOn the coarse-graining of polymers into bead-spring chainsJ Non-Newton Fluid Mech20041221–33311115.8235110.1016/j.jnnfm.2003.10.006 LodishHMolecular cell biology20045New York, NYW. H. Freeman and Company DamköhlerGStromungs und warmeubergangsprobleme in chemischer technik and forschungChem Ing Tech193912469 YuXPCarlssonAEKinetics of filament bundling with attractive interactionsBiophys J20048763679368910.1529/biophysj.104.047373 HeadDALevineAJMacKintoshFCDistinct regimes of elastic response and deformation modes of cross-linked cytoskeletal and semiflexible polymer networksPhys Rev E2003686061907061907 DalhaimerPDischerDELubenskyTCCrosslinked actin networks show liquid crystal elastomer behaviour, including soft-mode elasticityNat Phys20073535436010.1038/nphys567 CarlssonAEStimulation of actin polymerization by filament severingBiophys J200690241342210.1529/biophysj.105.069765 ChuJWVothGACoarse-grained modeling of the actin filament derived from atomistic-scale simulationsBiophys J20069051572158210.1529/biophysj.105.073924 NakayamaTYakuboKOrbachRLDynamical properties of fractal networks-scaling, numerical simulations, and physical realizationsRev Mod Phys199466238144310.1103/RevModPhys.66.381 IsambertHFlexibility of actin-filaments derived from thermal fluctuations-effect of bound nucleotide, phalloidin, and muscle regulatory proteinsJ Biol Chem199527019114371144410.1074/jbc.270.19.11437 GovNSGopinathanADynamics of membranes driven by actin polymerizationBiophys J200690245446910.1529/biophysj.105.062224 HowardJMechanics of motor proteins and the cytoskeleton2001Sunderland, MASinauer Associates TsengYThe bimodal role of filamin in controlling the architecture and mechanics of F-actin networksJ Biol Chem200427931819182610.1074/jbc.M306090200 KojimaHIshijimaAYanagidaTDirect measurement of stiffness of single actin-filaments with and without tropomyosin by in-vitro nanomanipulationP Natl Acad Sci USA19949126129621296610.1073/pnas.91.26.12962 J Howard (9091_CR1) 2001 J Belagyi (9091_CR44) 1983; 130 B Yap (9091_CR41) 2005; 98 KC Holmes (9091_CR26) 1990; 347 P Dalhaimer (9091_CR37) 2007; 3 R Shlomovitz (9091_CR16) 2007; 98 AE Carlsson (9091_CR11) 2006; 90 N Volkmann (9091_CR34) 2001; 153 B Wagner (9091_CR35) 2006; 103 Q Liao (9091_CR19) 2003; 36 9091_CR42 D Sept (9091_CR3) 2001; 81 KD Costa (9091_CR39) 2002; 52 H Isambert (9091_CR22) 1995; 270 H Isambert (9091_CR46) 1996; 29 MRK Mofrad (9091_CR5) 2006 R Yasuda (9091_CR25) 1996; 263 JKG Dhont (9091_CR43) 2003; 118 Y Tsuda (9091_CR24) 1996; 93 G Damköhler (9091_CR29) 1939; 12 H Higuchi (9091_CR21) 1995; 69 JW Chu (9091_CR8) 2005; 102 JA Cooper (9091_CR4) 1983; 22 F Gittes (9091_CR23) 1993; 120 Y Le (9091_CR7) 2006; 90 G Forgacs (9091_CR30) 1995; 108 GI Bell (9091_CR28) 1978; 200 Y Tseng (9091_CR38) 2004; 279 T Nakayama (9091_CR31) 1994; 66 H Lodish (9091_CR2) 2004 W Humphrey (9091_CR47) 1996; 14 T Oda (9091_CR45) 1998; 75 T Kreis (9091_CR6) 1999 NS Gov (9091_CR15) 2006; 90 D Sept (9091_CR10) 1999; 294 E Atilgan (9091_CR14) 2006; 90 9091_CR32 9091_CR33 XP Yu (9091_CR13) 2004; 87 TD Pollard (9091_CR27) 1986; 103 F Reif (9091_CR17) 1965 PT Underhill (9091_CR18) 2004; 122 MMAE Claessens (9091_CR36) 2006; 5 JW Chu (9091_CR9) 2006; 90 H Kojima (9091_CR20) 1994; 91 N Pender (9091_CR40) 1991; 100 XP Yu (9091_CR12) 2003; 85 |
References_xml | – volume: 153 start-page: 947 issue: 5 year: 2001 ident: 9091_CR34 publication-title: J Cell Biol doi: 10.1083/jcb.153.5.947 contributor: fullname: N Volkmann – volume: 22 start-page: 2193 issue: 9 year: 1983 ident: 9091_CR4 publication-title: Biochemistry doi: 10.1021/bi00278a021 contributor: fullname: JA Cooper – volume: 270 start-page: 11437 issue: 19 year: 1995 ident: 9091_CR22 publication-title: J Biol Chem doi: 10.1074/jbc.270.19.11437 contributor: fullname: H Isambert – volume: 98 start-page: 1930 issue: 5 year: 2005 ident: 9091_CR41 publication-title: J Appl Physiol doi: 10.1152/japplphysiol.01226.2004 contributor: fullname: B Yap – volume: 90 start-page: 65 issue: 1 year: 2006 ident: 9091_CR14 publication-title: Biophys J doi: 10.1529/biophysj.105.071480 contributor: fullname: E Atilgan – volume: 294 start-page: 1181 issue: 5 year: 1999 ident: 9091_CR10 publication-title: J Mol Biol doi: 10.1006/jmbi.1999.3332 contributor: fullname: D Sept – volume: 5 start-page: 748 issue: 9 year: 2006 ident: 9091_CR36 publication-title: Nat Mater doi: 10.1038/nmat1718 contributor: fullname: MMAE Claessens – volume: 75 start-page: 2672 issue: 6 year: 1998 ident: 9091_CR45 publication-title: Biophys J doi: 10.1016/S0006-3495(98)77712-4 contributor: fullname: T Oda – volume: 120 start-page: 923 issue: 4 year: 1993 ident: 9091_CR23 publication-title: J Cell Biol doi: 10.1083/jcb.120.4.923 contributor: fullname: F Gittes – volume: 12 start-page: 469 year: 1939 ident: 9091_CR29 publication-title: Chem Ing Tech contributor: fullname: G Damköhler – volume: 14 start-page: 33 issue: 1 year: 1996 ident: 9091_CR47 publication-title: J Mol Graph doi: 10.1016/0263-7855(96)00018-5 contributor: fullname: W Humphrey – volume: 200 start-page: 618 issue: 4342 year: 1978 ident: 9091_CR28 publication-title: Science doi: 10.1126/science.347575 contributor: fullname: GI Bell – volume: 66 start-page: 381 issue: 2 year: 1994 ident: 9091_CR31 publication-title: Rev Mod Phys doi: 10.1103/RevModPhys.66.381 contributor: fullname: T Nakayama – volume: 103 start-page: 2747 issue: 6 year: 1986 ident: 9091_CR27 publication-title: J Cell Biol doi: 10.1083/jcb.103.6.2747 contributor: fullname: TD Pollard – volume-title: Fundamentals of statistical and thermal physics year: 1965 ident: 9091_CR17 contributor: fullname: F Reif – volume: 90 start-page: 413 issue: 2 year: 2006 ident: 9091_CR11 publication-title: Biophys J doi: 10.1529/biophysj.105.069765 contributor: fullname: AE Carlsson – volume: 93 start-page: 12937 issue: 23 year: 1996 ident: 9091_CR24 publication-title: P Natl Acad Sci USA doi: 10.1073/pnas.93.23.12937 contributor: fullname: Y Tsuda – volume: 98 start-page: 168103 issue: 16 year: 2007 ident: 9091_CR16 publication-title: Phys Rev Lett doi: 10.1103/PhysRevLett.98.168103 contributor: fullname: R Shlomovitz – volume: 36 start-page: 3386 issue: 9 year: 2003 ident: 9091_CR19 publication-title: Macromolecules doi: 10.1021/ma025995f contributor: fullname: Q Liao – volume: 130 start-page: 353 issue: 2 year: 1983 ident: 9091_CR44 publication-title: Eur J Biochem doi: 10.1111/j.1432-1033.1983.tb07160.x contributor: fullname: J Belagyi – volume: 29 start-page: 1036 issue: 3 year: 1996 ident: 9091_CR46 publication-title: Macromolecules doi: 10.1021/ma946418x contributor: fullname: H Isambert – volume: 90 start-page: 1572 issue: 5 year: 2006 ident: 9091_CR9 publication-title: Biophys J doi: 10.1529/biophysj.105.073924 contributor: fullname: JW Chu – ident: 9091_CR32 doi: 10.1103/PhysRevLett.91.108102 – volume: 100 start-page: 187 year: 1991 ident: 9091_CR40 publication-title: J Cell Sci doi: 10.1242/jcs.100.1.187 contributor: fullname: N Pender – volume-title: Molecular cell biology year: 2004 ident: 9091_CR2 contributor: fullname: H Lodish – volume: 81 start-page: 667 issue: 2 year: 2001 ident: 9091_CR3 publication-title: Biophys J doi: 10.1016/S0006-3495(01)75731-1 contributor: fullname: D Sept – volume: 69 start-page: 1000 issue: 3 year: 1995 ident: 9091_CR21 publication-title: Biophys J doi: 10.1016/S0006-3495(95)79975-1 contributor: fullname: H Higuchi – volume: 52 start-page: 266 issue: 4 year: 2002 ident: 9091_CR39 publication-title: Cell Motil Cytoskel doi: 10.1002/cm.10056 contributor: fullname: KD Costa – volume: 108 start-page: 2131 year: 1995 ident: 9091_CR30 publication-title: J Cell Sci doi: 10.1242/jcs.108.6.2131 contributor: fullname: G Forgacs – volume-title: Mechanics of motor proteins and the cytoskeleton year: 2001 ident: 9091_CR1 contributor: fullname: J Howard – volume: 103 start-page: 13974 issue: 38 year: 2006 ident: 9091_CR35 publication-title: P Natl Acad Sci USA doi: 10.1073/pnas.0510190103 contributor: fullname: B Wagner – volume: 102 start-page: 13111 issue: 37 year: 2005 ident: 9091_CR8 publication-title: P Natl Acad Sci USA doi: 10.1073/pnas.0503732102 contributor: fullname: JW Chu – ident: 9091_CR33 doi: 10.1103/PhysRevE.68.061907 – volume-title: Cytoskeletal Mechanics year: 2006 ident: 9091_CR5 doi: 10.1017/CBO9780511607318 contributor: fullname: MRK Mofrad – volume: 90 start-page: 4295 issue: 12 year: 2006 ident: 9091_CR7 publication-title: Biophys J doi: 10.1529/biophysj.105.076968 contributor: fullname: Y Le – volume: 87 start-page: 3679 issue: 6 year: 2004 ident: 9091_CR13 publication-title: Biophys J doi: 10.1529/biophysj.104.047373 contributor: fullname: XP Yu – volume: 90 start-page: 454 issue: 2 year: 2006 ident: 9091_CR15 publication-title: Biophys J doi: 10.1529/biophysj.105.062224 contributor: fullname: NS Gov – volume: 263 start-page: 227 issue: 2 year: 1996 ident: 9091_CR25 publication-title: J Mol Biol doi: 10.1006/jmbi.1996.0571 contributor: fullname: R Yasuda – ident: 9091_CR42 doi: 10.1038/nature05824 – volume-title: Guidebook to the cytoskeletal and motor proteins year: 1999 ident: 9091_CR6 doi: 10.1093/oso/9780198599579.001.0001 contributor: fullname: T Kreis – volume: 347 start-page: 44 issue: 6288 year: 1990 ident: 9091_CR26 publication-title: Nature doi: 10.1038/347044a0 contributor: fullname: KC Holmes – volume: 3 start-page: 354 issue: 5 year: 2007 ident: 9091_CR37 publication-title: Nat Phys doi: 10.1038/nphys567 contributor: fullname: P Dalhaimer – volume: 279 start-page: 1819 issue: 3 year: 2004 ident: 9091_CR38 publication-title: J Biol Chem doi: 10.1074/jbc.M306090200 contributor: fullname: Y Tseng – volume: 85 start-page: 3532 issue: 6 year: 2003 ident: 9091_CR12 publication-title: Biophys J doi: 10.1016/S0006-3495(03)74773-0 contributor: fullname: XP Yu – volume: 122 start-page: 3 issue: 1–3 year: 2004 ident: 9091_CR18 publication-title: J Non-Newton Fluid Mech doi: 10.1016/j.jnnfm.2003.10.006 contributor: fullname: PT Underhill – volume: 118 start-page: 1466 issue: 3 year: 2003 ident: 9091_CR43 publication-title: J Chem Phys doi: 10.1063/1.1528912 contributor: fullname: JKG Dhont – volume: 91 start-page: 12962 issue: 26 year: 1994 ident: 9091_CR20 publication-title: P Natl Acad Sci USA doi: 10.1073/pnas.91.26.12962 contributor: fullname: H Kojima |
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SubjectTerms | Biomedical Engineering and Bioengineering Characterization and Evaluation of Materials Control Dynamical Systems Engineering Lasers Optical Devices Optics Photonics Solid Mechanics Vibration |
Title | Computational Analysis of a Cross-linked Actin-like Network |
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