Literature DB >> 17854206

Surface hydrophobicity modulates the operation of actomyosin-based dynamic nanodevices.

Dan V Nicolau1, Gerardin Solana, Murat Kekic, Florin Fulga, Chitladda Mahanivong, Jonathan Wright, Elena P Ivanova, Cristobal G dos Remedios.   

Abstract

We studied the impact of surface hydrophobicity on the motility of actin filaments moving on heavy-meromyosin (HMM)-coated surfaces. Apart from nitrocellulose (NC), which is the current standard for motility assays, all materials tested are good candidates for microfabrication: hydrophilic and hydrophobic glass, poly(methyl methacrylate) (PMMA), poly(tert-butyl methacrylate) (PtBuMA), and a copolymer of O-acryloyl acetophenone oxime with a 4-acryloyloxybenzophenone (AAPO). The most hydrophilic (hydrophilic glass, contact angle 35 degrees) and the most hydrophobic (PtBuMA, contact angle 78 degrees) surfaces do not maintain the motility of actin filaments, presumably because of the low density of adsorbed HMM protein or its high levels of denaturation, respectively. The velocity of actin filaments presents higher values in the middle of this "surface hydrophobicity motility window" (NC, PMMA), and a bimodal distribution, which is more apparent at the edges of this motility window (hydrophobic glass and AAPO). A molecular surface analysis of HMM and its S1 units suggests that the two very different, temporally separated conformations of the HMM heads could exacerbate the surface-modulated protein behavior, which is common to all microdevices using surface-immobilized proteins. An explanation for the above behavior proposes that the motility of actin filaments on HMM-functionalized surfaces is the result of the action of three populations of motors, each in a different surface-protein conformation, that is, HMM with both heads working (high velocities), working with one head (low velocities), and fully denatured HMM (no motility). It is also proposed that the molecularly dynamic nature of polymer surfaces amplifies the impact of surface hydrophobicity on protein behavior. The study demonstrates that PMMA is a good candidate for the fabrication of future actomyosin-driven dynamic nanodevices because it induces the smoothest motility of individual nano-objects with velocities comparable with those obtained on NC.

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Year:  2007        PMID: 17854206     DOI: 10.1021/la700412m

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  7 in total

Review 1.  Translational actomyosin research: fundamental insights and applications hand in hand.

Authors:  Alf Månsson
Journal:  J Muscle Res Cell Motil       Date:  2012-05-26       Impact factor: 2.698

2.  Positional Isomers of a Non-Nucleoside Substrate Differentially Affect Myosin Function.

Authors:  Mike Woodward; Eric Ostrander; Seung P Jeong; Xiarong Liu; Brent Scott; Matt Unger; Jianhan Chen; Dhandapani Venkataraman; Edward P Debold
Journal:  Biophys J       Date:  2020-06-30       Impact factor: 4.033

3.  Long-term storage of surface-adsorbed protein machines.

Authors:  Nuria Albet-Torres; Alf Månsson
Journal:  Langmuir       Date:  2011-05-12       Impact factor: 3.882

4.  High-Resolution Imaging of a Single Gliding Protofilament of Tubulins by HS-AFM.

Authors:  Jakia Jannat Keya; Daisuke Inoue; Yuki Suzuki; Toshiya Kozai; Daiki Ishikuro; Noriyuki Kodera; Takayuki Uchihashi; Arif Md Rashedul Kabir; Masayuki Endo; Kazuki Sada; Akira Kakugo
Journal:  Sci Rep       Date:  2017-07-21       Impact factor: 4.379

5.  Comparative analysis of widely used methods to remove nonfunctional myosin heads for the in vitro motility assay.

Authors:  Mohammad A Rahman; Aseem Salhotra; Alf Månsson
Journal:  J Muscle Res Cell Motil       Date:  2019-03-08       Impact factor: 2.698

6.  Protein molecular surface mapped at different geometrical resolutions.

Authors:  Dan V Nicolau; Ewa Paszek; Florin Fulga; Dan V Nicolau
Journal:  PLoS One       Date:  2013-03-14       Impact factor: 3.240

7.  Sensing surface mechanical deformation using active probes driven by motor proteins.

Authors:  Daisuke Inoue; Takahiro Nitta; Arif Md Rashedul Kabir; Kazuki Sada; Jian Ping Gong; Akihiko Konagaya; Akira Kakugo
Journal:  Nat Commun       Date:  2016-10-03       Impact factor: 14.919

  7 in total

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