Electrophoresis of individual microtubules in microchannels
Open accessAbstract
We use micrometer-sized fluidic channels to confine and measure electrophoresis of freely suspended individual microtubules. We measure orientation-dependent velocities of microtubules and the electro-osmotic flow mobility in our channels to infer the anisotropic electrophoretic mobility of microtubules under physiological conditions. We discuss the difference between electrophoresis and purely hydrodynamic motion and its implications for interpreting mobility measurements. We show that the mobility anisotropy is a factor of 0.83, clearly different from the well known anisotropy factor of 0.5 in Stokes drag coefficients for cylindrical objects. We also show that the velocity is independent of microtubule length, which would be different for hydrodynamic motion. We demonstrate that the electric force on the counterions has important consequences for the interpretation of electrophoresis experiments and that ignoring this can lead to an underestimation of the effective charge by orders of magnitude. From the electrophoresis measurements, we calculate an effective surface-charge density of -36.7 +/- 0.4 mC/m2 for microtubules. Electrophoretic measurements of subtilisin-digested microtubules, which have the negatively charged C termini on the outer surface removed, show a 24% decrease in mobility and, correspondingly, in surface charge, but no change in anisotropy.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Like MTs, AFs can be manipulated by external electric fields.
“Like MTs [96], AFs can be manipulated by external electric fields [113].”
From An Overview of Sub-Cellular Mechanisms Involved in the Action of TTFields (2016) · cites this paper as [96]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Intermolecular and Surface Forces
(2011) · Elsevier eBooks · doi:10.1016/b978-0-12-391927-4.10024-6 · Cited by 17,234 · see citing works
Structure of the αβ tubulin dimer by electron crystallography
Nogales, E., Wolf, S., & Downing, K. (1998) · Nature · doi:10.1038/34465 · Cited by 1,623 · see citing works
High-Resolution Model of the Microtubule
Nogales, E., Whittaker, M., Milligan, R. A., & Downing, K. H. (1999) · Cell · doi:10.1016/s0092-8674(00)80961-7 · Cited by 1,200 · see citing works
The cataphoresis of suspended particles. Part I.—The equation of cataphoresis
Henry, D. C. (1931) · Proceedings of the Royal Society of London Series A Containing Papers of a Mathematical and Physical Character · doi:10.1098/rspa.1931.0133 · Cited by 983 · see citing works
Calculation of the electrophoretic mobility of a spherical colloid particle
Wiersema, P. H., Loeb, A. L., & Overbeek, J. T. G. (1966) · Journal of Colloid and Interface Science · doi:10.1016/0021-9797(66)90069-5 · Cited by 840 · see citing works
Electrophoresis of DNA and other polyelectrolytes: Physical mechanisms
Viovy, J. (2000) · Reviews of Modern Physics · doi:10.1103/revmodphys.72.813 · Cited by 723 · see citing works
Streaming Currents in a Single Nanofluidic Channel
van der Heyden, F. H. J., Stein, D., & Dekker, C. (2005) · Physical Review Letters · doi:10.1103/physrevlett.95.116104 · Cited by 547 · see citing works
Self-citationHuang, X. C., Gordon, M. J., & Zare, R. N. (1988) · Analytical Chemistry · doi:10.1021/ac00168a040 · Cited by 489 · see citing works
The force exerted by a single kinesin molecule against a viscous load
Hunt, A. J., Gittes, F., & Howard, J. (1994) · Biophysical Journal · doi:10.1016/s0006-3495(94)80537-5 · Cited by 344 · see citing works
Complete amino acid sequence of beta-tubulin from porcine brain.
Krauhs, E., Little, M., Kempf, T., Hofer-Warbinek, R., Ade, W., & Ponstingl, H. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.7.4156 · Cited by 305 · see citing works
Complete amino acid sequence of alpha-tubulin from porcine brain.
Ponstingl, H., Krauhs, E., Little, M., & Kempf, T. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.5.2757 · Cited by 272 · see citing works
Molecular Sorting by Electrical Steering of Microtubules in Kinesin-Coated Channels
van den Heuvel, M. G. L., de Graaff, M. P., & Dekker, C. (2006) · Science · doi:10.1126/science.1124258 · Cited by 244 · see citing works
Self-citationErratum: Structure of the αβ tubulin dimer by electron crystallography
Nogales, E., Wolf, S. G., & Downing, K. H. (1998) · Nature · doi:10.1038/30288 · Cited by 227 · see citing works
Viscous force and torque constants for a cylinder
Broersma, S. (1981) · The Journal of Chemical Physics · doi:10.1063/1.441071 · Cited by 197 · see citing works
Elastic Response, Buckling, and Instability of Microtubules under Radial Indentation
Schaap, I. A. T., Carrasco, C., de Pablo, P. J., MacKintosh, F. C., & Schmidt, C. F. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.077826 · Cited by 175 · see citing works
Acting on actin: the electric motility assay
Riveline, D., Ott, A., Jülicher, F., Winkelmann, D. A., Cardoso, O., Lacapère, J.-J., Magnúsdóttir, S., Viovy, J., Talini, L., & Prost, J. (1998) · European Biophysics Journal · doi:10.1007/s002490050147 · Cited by 151 · see citing works
Redeker, V., Melki, R., Promé, D., Caër, J. L., & Rossier, J. (1992) · FEBS Letters · doi:10.1016/0014-5793(92)81441-n · Cited by 148 · see citing works
Analysis of the migration behaviour of single microtubules in electric fields
Stracke, R., Böhm, K. J., Wollweber, L., Tuszynski, J. A., & Unger, E. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00251-6 · Cited by 147 · see citing works
Tubulin, hybrid dimers, and tubulin S. Stepwise charge reduction and polymerization.
Bhattacharyya, B., Sackett, D. L., & Wolff, J. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)39233-5 · Cited by 128 · see citing works
Microscale Transport and Sorting by Kinesin Molecular Motors
Jia, L., Moorjani, S. G., Jackson, T. N., & Hancock, W. O. (2004) · Biomedical Microdevices · doi:10.1023/b:bmmd.0000013368.89455.8d · Cited by 122 · see citing works
Stigter, D. (1978) · The Journal of Physical Chemistry · doi:10.1021/j100501a019 · Cited by 109 · see citing works
Henry's Function for Electrophoresis of a Cylindrical Colloidal Particle
Ohshima, H. (1996) · Journal of Colloid and Interface Science · doi:10.1006/jcis.1996.0305 · Cited by 108 · see citing works
A note on the screening of hydrodynamic interactions, in electrophoresis, and in porous media
Long, D., & Ajdari, A. (2001) · The European Physical Journal E · doi:10.1007/s101890170139 · Cited by 98 · see citing works
Proteolysis of tubulin and the substructure of the tubulin dimer.
Sackett, D. L., & Wolff, J. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)84489-7 · Cited by 92 · see citing works
Stigter, D. (1978) · The Journal of Physical Chemistry · doi:10.1021/j100501a020 · Cited by 71 · see citing works
High-Throughput Single-Molecule DNA Screening Based on Electrophoresis
Shortreed, M. R., Li, H., Huang, W., & Yeung, E. S. (2000) · Analytical Chemistry · doi:10.1021/ac991428n · Cited by 69 · see citing works
Bittl, J. A., Weisfeldt, M. L., & Jacobus, W. E. (1985) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)89717-4 · Cited by 66 · see citing works
Movement and Alignment of Microtubules in Electric Fields and Electric-Dipole-Moment Estimates
Böhm, K. J., Mavromatos, N. E., Michette, A. G., Stracke, R., & Unger, E. (2005) · Electromagnetic Biology and Medicine · doi:10.1080/15368370500380010 · Cited by 50 · see citing works
Theory of conductance of colloidal electrolytes in univalent salt solutions
Stigter, D. (1979) · The Journal of Physical Chemistry · doi:10.1021/j100475a017 · Cited by 19 · see citing works
MacConnell, D. J. (1967) · The Astronomical Journal · doi:10.1086/110330 · Cited by 14 · see citing works
Single filament electrophoresis of F-actin and filamentous virus fd
Li, G., Wen, Q., & Tang, J. X. (2005) · The Journal of Chemical Physics · doi:10.1063/1.1859284 · Cited by 11 · see citing works
Flagged first, then by citations
Research works printed but not linked: 13
- [4]Stigter D. J Phys Chem. 1978;82:1417–1423. [Google Scholar]
- [6]Henry D. Proc R Soc London Ser A. 1933;133:106–129. [Google Scholar]
- [7]Viovy JL. Rev Mod Phys. 2000;72:813–872. [Google Scholar]
- [10]Long D, Ajdari A. Eur Phys J E. 2001;4:29–32. [Google Scholar]
- [11]Ohshima H. J Colloid Interface Sci. 1996;180:299–301. [Google Scholar]
- [12]Wiersema PH, Loeb AL, Overbeek JT. J Colloid Interface Sci. 1966;22:78–99. [Google Scholar]
- [13]Stigter D. J Phys Chem. 1978;82:1424–1429. [Google Scholar]
- [14]Huang XH, Gordon MJ, Zare RN. Anal Chem. 1988;60:1837–1838. [Google Scholar]
- [15]Bohm KJ, Mavromatos NE, Michette A, Stracke R, Unger E. Electromagn Biol And Med. 2005;24:319–330. [Google Scholar]
- [16]Broersma S. J Chem Phys. 1981;74:6989–6990. [Google Scholar]
- [24]Sackett DL, Wolff J. J Biol Chem. 1986;261:9070–9076. [PubMed] [Google Scholar]
- [26]Bhattacharyya B, Sackett DL, Wolff J. J Biol Chem. 1985;260:208–216. [PubMed] [Google Scholar]
- [27]Stigter D. J Phys Chem. 1979;83:1663–1670. [Google Scholar]
Cited by
Sorted by citations
Effect of Joule heating on electrokinetic transport
Çetin, B., & Li, D. (2008) · Electrophoresis · doi:10.1002/elps.200700601 · Cited by 116 · see citing works
An Overview of Sub-Cellular Mechanisms Involved in the Action of TTFields
Tuszynski, J., Wenger, C., Friesen, D., & Preto, J. (2016) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph13111128 · Cited by 95 · see citing works
Microtubule curvatures under perpendicular electric forces reveal a low persistence length
Van den Heuvel, M. G. L., de Graaff, M. P., & Dekker, C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704169105 · Cited by 88 · see citing works
Self-citationPagonabarraga, I., Rotenberg, B., & Frenkel, D. (2010) · Physical Chemistry Chemical Physics · doi:10.1039/c004012f · Cited by 82 · see citing works
Hilitski, F., Ward, A. R., Cajamarca, L., Hagan, M. F., Grason, G. M., & Dogic, Z. (2015) · Physical Review Letters · doi:10.1103/physrevlett.114.138102 · Cited by 68 · see citing works
A DNA turbine powered by a transmembrane potential across a nanopore
Shi, X., Pumm, A.-K., Maffeo, C., Köhler, F., Feigl, E., Zhao, W.-X., Verschueren, D. V., Golestanian, R., Aksimentiev, A., Dietz, H., et al. (2023) · Nature Nanotechnology · doi:10.1038/s41565-023-01527-8 · Cited by 66 · see citing works
Self-citationAll Wired Up: An Exploration of the Electrical Properties of Microtubules and Tubulin
Kalra, A. P., Eakins, B. B., Patel, S. D., Ciniero, G., Rezania, V., Shankar, K., & Tuszynski, J. A. (2020) · ACS Nano · doi:10.1021/acsnano.0c06945 · Cited by 49 · see citing works
Chung, P. J., Choi, M. C., Miller, H. P., Feinstein, H. E., Raviv, U., Li, Y., Wilson, L., Feinstein, S. C., & Safinya, C. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513172112 · Cited by 49 · see citing works
Biological wires, communication systems, and implications for disease
Friesen, D. E., Craddock, T. J. A., Kalra, A. P., & Tuszynski, J. A. (2015) · Biosystems · doi:10.1016/j.biosystems.2014.10.006 · Cited by 48 · see citing works
Dynamics of wormlike and glassy wormlike chains
Kroy, K. (2008) · Soft Matter · doi:10.1039/b807018k · Cited by 31 · see citing works
Fuwad, A., Ryu, H., Han, E. D., Lee, J., Malmstadt, N., Kim, Y., Seo, Y. H., Kim, S. M., & Jeon, T. (2024) · npj Clean Water · doi:10.1038/s41545-024-00301-0 · Cited by 29 · see citing works
Investigation of the Electrical Properties of Microtubule Ensembles under Cell-Like Conditions
Kalra, A. P., Patel, S., Bhuiyan, A., Preto, J., Scheuer, K. G., Mohammed, U., Lewis, J. D., Rezania, V., Shankar, K., & Tuszyński, J. A. (2020) · Nanomaterials · doi:10.3390/nano10020265 · Cited by 29 · see citing works
Modeling electrokinetic flows by the smoothed profile method
Luo, X., Beşkök, A., & Karniadakis, G. E. (2010) · Journal of Computational Physics · doi:10.1016/j.jcp.2010.01.030 · Cited by 27 · see citing works
Chierici, F., Dogariu, A. C., & Tuszyński, J. A. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.884043 · Cited by 26 · see citing works
Single Centrosome Manipulation Reveals Its Electric Charge and Associated Dynamic Structure
Hormeño, S., Ibarra, B., Chichón, F. J., Habermann, K., Lange, B. M. H., Valpuesta, J., Carrascosa, J. L., & Arias‐Gonzalez, J. R. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.06.004 · Cited by 24 · see citing works
Cooperative lattice dynamics and anomalous fluctuations of microtubules
Mohrbach, H., Johner, A., & Kulić, I. M. (2011) · European Biophysics Journal · doi:10.1007/s00249-011-0778-0 · Cited by 23 · see citing works
Microelectrophoresis of Silica Rods Using Confocal Microscopy
Bakker, H. E., Besseling, T. H., Wijnhoven, J. E. G. J., Helfferich, P., van Blaaderen, A., & Imhof, A. (2017) · Langmuir · doi:10.1021/acs.langmuir.6b03863 · Cited by 23 · see citing works
Single-Molecule Observation of Anomalous Electrohydrodynamic Orientation of Microtubules
van den Heuvel, M. G. L., Bondesan, R., Lagomarsino, M. C., & Dekker, C. (2008) · Physical Review Letters · doi:10.1103/physrevlett.101.118301 · Cited by 22 · see citing works
Self-citationElectrophoresis-Based Adaptive Manipulation of Nanowires in Fluid Suspension
Wu, J., Li, X.-L., & Yu, K. (2020) · IEEE/ASME Transactions on Mechatronics · doi:10.1109/tmech.2020.2974379 · Cited by 22 · see citing works
Modeling Microtubule Counterion Distributions and Conductivity Using the Poisson-Boltzmann Equation
Eakins, B. B., Patel, S., Kalra, A. P., Rezania, V., Shankar, K., & Tuszyński, J. A. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.650757 · Cited by 22 · see citing works
Inhibition of Microtubule Depolymerization by Osmolytes
Bachand, G. D., Jain, R., Ko, R., Bouxsein, N. F., & VanDelinder, V. (2018) · Biomacromolecules · doi:10.1021/acs.biomac.7b01799 · Cited by 19 · see citing works
Models of protein linear molecular motors for dynamic nanodevices
Fulga, F., Nicolau, D. V., & Nicolau, D. V. (2008) · Integrative Biology · doi:10.1039/b814985b · Cited by 18 · see citing works
Freely relaxing polymers remember how they were straightened
Obermayer, B., Möbius, W., Hallatschek, O., Frey, E., & Kroy, K. (2009) · Physical Review E · doi:10.1103/physreve.79.021804 · Cited by 17 · see citing works
Single Filament Behavior of Microtubules in the Presence of Added Divalent Counterions
Bouxsein, N. F., & Bachand, G. D. (2014) · Biomacromolecules · doi:10.1021/bm500988r · Cited by 14 · see citing works
Roadmap for network-based biocomputation
van Delft, F. C. M. J. M., Månsson, A., Kugler, H., Korten, T., Reuther, C., Zhu, J., Lyttleton, R. W., Blaudeck, T., Meinecke, C., Reuter, D., et al. (2022) · Nano Futures · doi:10.1088/2399-1984/ac7d81 · Cited by 13 · see citing works
Wu, J., & Yu, K. (2022) · IEEE Transactions on Automation Science and Engineering · doi:10.1109/tase.2022.3187956 · Cited by 12 · see citing works
Lab-on-chip microscope platform for electro-manipulation of a dense microtubules network
Havelka, D., Zhernov, I., Teplan, M., Lánský, Z., Chafai, D. E., & Cifra, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-06255-y · Cited by 11 · see citing works
Gregorio, E. D., Staelens, M., Hosseinkhah, N., Karimpoor, M., Liburd, J., Lim, L., Shankar, K., & Tuszyński, J. A. (2024) · Nanomaterials · doi:10.3390/nano14131093 · Cited by 10 · see citing works
Mousavidoust, S., Mobasheri, H., & Riazi, G. H. (2016) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2016.1254683 · Cited by 10 · see citing works
A Nanometric Probe of the Local Proton Concentration in Microtubule-Based Biophysical Systems
Kalra, A. P., Eakins, B. B., Vagin, S. I., Wang, H., Patel, S., Winter, P., Aminpour, M., Lewis, J. D., Rezania, V., Shankar, K., et al. (2021) · Nano Letters · doi:10.1021/acs.nanolett.1c04487 · Cited by 9 · see citing works
Motorless transport of microtubules along tubulin, RanGTP, and salt gradients
Shim, S., Gouveia, B., Ramm, B., Valdez, V. A., Petry, S., & Stone, H. A. (2024) · Nature Communications · doi:10.1038/s41467-024-53656-w · Cited by 8 · see citing works
Functional localization of kinesin/microtubule-based motility system along metallic glass microwires
Kim, K., Sikora, A., Nakayama, K. S., Nakazawa, H., Umetsu, M., Hwang, W., & Teizer, W. (2014) · Applied Physics Letters · doi:10.1063/1.4896964 · Cited by 8 · see citing works
Simulations of polyelectrolyte dynamics in an externally applied electric field in confined geometry
Nedelcu, S., & Sommer, J. (2010) · The Journal of Chemical Physics · doi:10.1063/1.3509390 · Cited by 8 · see citing works
Wu, J., & Yu, K. (2020) · IFAC-PapersOnLine · doi:10.1016/j.ifacol.2020.12.516 · Cited by 8 · see citing works
Revealing and Attenuating the Electrostatic Properties of Tubulin and Its Polymers
Kalra, A. P., Patel, S., Eakins, B. B., Riddell, S., Kumar, P., Winter, P., Preto, J., Carlson, K. W., Lewis, J. D., Rezania, V., et al. (2020) · Small · doi:10.1002/smll.202003560 · Cited by 8 · see citing works
Accurate simulation dynamics of microscopic filaments using “caterpillar” Oseen hydrodynamics
Bailey, A. G., Lowe, C., Pagonabarraga, I., & Lagomarsino, M. C. (2009) · Physical Review E · doi:10.1103/physreve.80.046707 · Cited by 7 · see citing works
No observable non-thermal effect of microwave radiation on the growth of microtubules
Hammarin, G., Norder, P., Harimoorthy, R., Chen, G., Berntsen, P., Widlund, P. O., Stoij, C., Rodilla, H., Swenson, J., Brändén, G., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-68852-3 · Cited by 6 · see citing works
Electrodiffusiophoresis of a large- zeta -potential particle in weak fields
Tricoli, V., & Orsini, G. (2015) · Journal of Physics Condensed Matter · doi:10.1088/0953-8984/27/41/415102 · Cited by 6 · see citing works
Electrical behaviour and evolutionary computation in thin films of bovine brain microtubules
Vissol-Gaudin, E., Pearson, C., Groves, C., Zeze, D. A., Cantiello, H. F., Cantero, M. D. R., & Petty, M. C. (2021) · Scientific Reports · doi:10.1038/s41598-021-90260-0 · Cited by 6 · see citing works
Prospects for single-molecule electrostatic detection in molecular motor gliding motility assays
Miranda, M., Lyttleton, R. W., Siu, P. H., Diez, S., Linke, H., & Micolich, A. P. (2021) · New Journal of Physics · doi:10.1088/1367-2630/abfdf5 · Cited by 5 · see citing works
Electrophoretic mobility of spherical particles in bounded domain
Liu, Y., Pennathur, S., & Meinhart, C. D. (2015) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2015.08.039 · Cited by 5 · see citing works
Electric field-induced reversible trapping of microtubules along metallic glass microwire electrodes
Kim, K., Sikora, A., Nakayama, K. S., Umetsu, M., Hwang, W., & Teizer, W. (2015) · Journal of Applied Physics · doi:10.1063/1.4917203 · Cited by 5 · see citing works
On the flow field about an electrophoretic particle
Orsini, G., & Tricoli, V. (2012) · Physics of Fluids · doi:10.1063/1.4757015 · Cited by 5 · see citing works
Li, X., Liu, K., Fang, H., Liu, Z., Tang, Y., & Dai, P. (2024) · APL Bioengineering · doi:10.1063/5.0197900 · Cited by 4 · see citing works
Electrophoresis-Based Manipulation of Micro- and Nanoparticles in Fluid Suspensions
Yu, K. (2021) · Springer eBooks · doi:10.1007/978-3-030-80197-7_6 · Cited by 4 · see citing works
Transport of Ions, DNA Polymers, and Microtubules in the Nanofluidic Regime
Stein, D., van den Heuvel, M. G. L., & Dekker, C. (2016) · Royal Society of Chemistry eBooks · doi:10.1039/9781849735230-00001 · Cited by 4 · see citing works
Self-citationThe effects of external electric fields on proteins
Cifra, M., Pandey, S. K., Zakar, T., Poplová, M., Campoy, D. G. B., Průša, J., Havelka, D., Marracino, P., Liberti, M., Apollonio, F., et al. (2026) · Chemical Society Reviews · doi:10.1039/d3cs00244f · Cited by 4 · see citing works
Dixit, A., Parashar, C. K., Dutta, S., Mahanta, J., Kakati, N., & Bandyopadhyay, D. (2021) · Electrophoresis · doi:10.1002/elps.202100152 · Cited by 3 · see citing works
Purcell factors and Förster-resonance energy transfer in proximity to helical structures
Farhi, A., & Dogariu, A. C. (2022) · Physical Review A · doi:10.1103/physreva.106.013708 · Cited by 3 · see citing works
Nanoscale electromagnetic field interaction generated by microtubule vibration in neurons
Wang, Y., Wang, L., & Wu, J.-Z. (2021) · Acta Physica Sinica · doi:10.7498/aps.70.20210421 · Cited by 3 · see citing works
Role of microtubules in neuro-electrical transmission
Zhu, B. T. (2022) · Brain Network and Modulation · doi:10.4103/2773-2398.365025 · Cited by 2 · see citing works
Mechanical Stimulation‐Induced Orientation of Gliding Microtubules in Confined Microwells
Inoue, D., Kabir, A. M. R., Tokuraku, K., Sada, K., & Kakugo, A. (2020) · Advanced Materials Interfaces · doi:10.1002/admi.201902013 · Cited by 2 · see citing works
Dynamic and electrophoretic light scattering measurements on microtubules at low concentrations
George, A., Alva, E., Brancaleon, L., & Marucho, M. (2024) · PLoS ONE · doi:10.1371/journal.pone.0312430 · Cited by 1 · see citing works
Nanoscale Components of Neurons: From Biomolecules to Nanodevices
Woolf, N. J., Priel, A., & Tuszyński, J. A. (2009) · Biological and medical physics series · doi:10.1007/978-3-642-03584-5_2 · Cited by 1 · see citing works
[Study on the mesoscopic dynamic effects of tumor treating fields on cell tubulin].
Li, X., Liu, K., Guo, C., Fang, T., & Yang, F. (2024) · PubMed Central · doi:10.7507/1001-5515.202312063 · Cited by 1 · see citing works
NAKAHARA, T., Isozaki, N., Suguru, A. N. D. O., Kamisetty, N. K., Shintaku, H., Kotera, H., & Yokokawa, R. (2014) · IEEJ Transactions on Sensors and Micromachines · doi:10.1541/ieejsmas.134.64
Analysis of Electromigration in Nanofluidics
Liu, Y. (2015) · eScholarship (California Digital Library)
Cooperative Lattice Dynamics and Anomalous Fluctuations of MicrotubulesPreprint
Mohrbach, H., Johner, A., & Kulić, I. M. (2011) · arXiv (Cornell University) · doi:10.48550/arxiv.1108.4800
Palicha, K. A., Loganathan, P., Sudha, V., & Harinipriya, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-36902-x
Lieberwirth, E., Schaeper, A., Lange, R., Barke, I., Baltrusch, S., & Speller, S. (2025) · Beilstein Journal of Nanotechnology · doi:10.3762/bjnano.16.73
Samghabadi, F. S., McGovern, A. D., Edimeh, P., Robertson‐Anderson, R. M., & Conrad, J. C. (2025) · ACS Macro Letters · doi:10.1021/acsmacrolett.5c00633
- Authors
- van den Heuvel, M. G. L., de Graaff, M. P., Lemay, S. G., & Dekker, C.
- Affiliations
- Kavli Institute of Nanoscience, Delft University of Technology, Lorentzweg 1, 2628 CJ, Delft, The Netherlands
- Delft University of Technology (NL)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-05-08
- Volume
- 104
- Issue
- 19
- Pages
- 7770-7775
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1876522
- OpenAlex
- W2109115241
- Cited by
- 62
- References
- 31
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 7 · 2023: 2 · 2022: 7 · 2021: 7 · 2020: 6 · 2018: 1 · 2017: 1 · 2016: 3 · 2015: 6 · 2014: 4 · 2012: 1
- FWCI
- 2.62
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Electrostatics and Colloid Interactions
- Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Capillary Electrophoresis Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Keywords
- microtubules, electrophoresis, microchannels, electroosmotic flow, surface charge density, hydrodynamic motion, subtilisin digestion, Stokes drag
- MeSH terms
- Electrophoresis, Microtubules, Solutions, Surface Properties, Tubulin, Anisotropy, Dimerization
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review