A Quantitative Comparison of Single-Dye Tracking Analysis Tools Using Monte Carlo Simulations

Single-particle tracking (SPT) is widely used to study processes from membrane receptor organization to the dynamics of RNAs in living cells. While single-dye labeling strategies have the benefit of being minimally invasive, this comes at the expense of data quality; typically a data set of short trajectories is obtained and analyzed by means of the mean square displacements (MSD) or the distribution of the particles’ displacements in a set time interval (jump distance, JD). To evaluate the applicability of both approaches, a quantitative comparison of both methods under typically encountered experimental conditions is necessary. Here we use Monte Carlo simulations to systematically compare the accuracy of diffusion coefficients (D-values) obtained for three cases: one population of diffusing species, two populations with different D-values, and a population switching between two D-values. For the first case we find that the MSD gives more or equally accurate results than the JD analysis (relative errors of D-values <6%). If two diffusing species are present or a particle undergoes a motion change, the JD analysis successfully distinguishes both species (relative error <5%). Finally we apply the JD analysis to investigate the motion of endogenous LPS receptors in live macrophages before and after treatment with methyl-β-cyclodextrin and latrunculin B.

[1]  J. Westwater,et al.  The Mathematics of Diffusion. , 1957 .

[2]  W. Webb,et al.  Diffusion of low density lipoprotein-receptor complex on human fibroblasts , 1982, The Journal of cell biology.

[3]  R. Steinman,et al.  Specific antimononuclear phagocyte monoclonal antibodies. Application to the purification of dendritic cells and the tissue localization of macrophages , 1983, The Journal of experimental medicine.

[4]  S. Goyert,et al.  The monocyte differentiation antigen, CD14, is anchored to the cell membrane by a phosphatidylinositol linkage. , 1988, Journal of immunology.

[5]  H. Qian,et al.  Single particle tracking. Analysis of diffusion and flow in two-dimensional systems. , 1991, Biophysical journal.

[6]  R. Cherry,et al.  Tracking of cell surface receptors by fluorescence digital imaging microscopy using a charge-coupled device camera. Low-density lipoprotein and influenza virus receptor mobility at 4 degrees C. , 1992, Journal of cell science.

[7]  M. Saxton,et al.  Single-particle tracking: models of directed transport. , 1994, Biophysical journal.

[8]  D. Grier,et al.  Methods of Digital Video Microscopy for Colloidal Studies , 1996 .

[9]  W. Webb,et al.  Constrained diffusion or immobile fraction on cell surfaces: a new interpretation. , 1996, Biophysical journal.

[10]  K. Jacobson,et al.  Single-particle tracking: applications to membrane dynamics. , 1997, Annual review of biophysics and biomolecular structure.

[11]  M. Saxton Single-particle tracking: the distribution of diffusion coefficients. , 1997, Biophysical journal.

[12]  H Schindler,et al.  Single-molecule microscopy on model membranes reveals anomalous diffusion. , 1997, Biophysical journal.

[13]  G. Schütz,et al.  Free Brownian motion of individual lipid molecules in biomembranes. , 1999, Biophysical journal.

[14]  B. Beutler,et al.  Tlr4: central component of the sole mammalian LPS sensor. , 2000, Current opinion in immunology.

[15]  S. Simon,et al.  Tracking single proteins within cells. , 2000, Biophysical journal.

[16]  M K Cheezum,et al.  Quantitative comparison of algorithms for tracking single fluorescent particles. , 2001, Biophysical journal.

[17]  F. Gusovsky,et al.  Inhibition of Endotoxin Response by E5564, a Novel Toll-Like Receptor 4-Directed Endotoxin Antagonist , 2003, Journal of Pharmacology and Experimental Therapeutics.

[18]  H. Spaink,et al.  In vivo plasma membrane organization: results of biophysical approaches. , 2004, Biochimica et biophysica acta.

[19]  T. Hartung,et al.  Lateral diffusion of Toll-like receptors reveals that they are transiently confined within lipid rafts on the plasma membrane , 2004, Journal of Cell Science.

[20]  M. Saxton,et al.  Membrane lateral mobility obstructed by polymer-tethered lipids studied at the single molecule level. , 2005, Biophysical journal.

[21]  P. Koumoutsakos,et al.  Feature point tracking and trajectory analysis for video imaging in cell biology. , 2005, Journal of structural biology.

[22]  W E Moerner,et al.  Cholesterol depletion suppresses the translational diffusion of class II major histocompatibility complex proteins in the plasma membrane. , 2005, Biophysical journal.

[23]  R. Tsien,et al.  The Fluorescent Toolbox for Assessing Protein Location and Function , 2006, Science.

[24]  Y. Henis,et al.  Cyclodextrins but not Compactin Inhibit the Lateral Diffusion of Membrane Proteins Independent of Cholesterol , 2006, Traffic.

[25]  Gernot Guigas,et al.  Size-dependent diffusion of membrane inclusions. , 2006, Biophysical journal.

[26]  D. Klenerman,et al.  Nanopipette delivery of individual molecules to cellular compartments for single-molecule fluorescence tracking. , 2007, Biophysical journal.

[27]  Gerhard J Schütz,et al.  (Un)confined diffusion of CD59 in the plasma membrane determined by high-resolution single molecule microscopy. , 2007, Biophysical journal.

[28]  G. Mashanov,et al.  Automatic detection of single fluorophores in live cells. , 2007, Biophysical journal.

[29]  F. Dumas,et al.  Functional membrane diffusion of G-protein coupled receptors , 2007, European Biophysics Journal.

[30]  Mingzhai Sun,et al.  The effect of cellular cholesterol on membrane-cytoskeleton adhesion , 2007, Journal of Cell Science.

[31]  H. Leonhardt,et al.  Probing Intranuclear Environments at the Single-Molecule Level , 2007, Biophysical journal.

[32]  H. Leonhardt,et al.  Discontinuous movement of mRNP particles in nucleoplasmic regions devoid of chromatin , 2008, Proceedings of the National Academy of Sciences.

[33]  A. Sergé,et al.  Dynamic multiple-target tracing to probe spatiotemporal cartography of cell membranes , 2008, Nature Methods.

[34]  Michael Z. Lin,et al.  Improving the photostability of bright monomeric orange and red fluorescent proteins , 2008, Nature Methods.

[35]  K. Lidke,et al.  Actin restricts FcɛRI diffusion and facilitates antigen-induced receptor immobilization , 2008, Nature Cell Biology.

[36]  K. Jaqaman,et al.  Robust single particle tracking in live cell time-lapse sequences , 2008, Nature Methods.

[37]  Michael J Saxton,et al.  Single-particle tracking: connecting the dots , 2008, Nature Methods.

[38]  Gerhard J Schütz,et al.  Versatile analysis of single-molecule tracking data by comprehensive testing against Monte Carlo simulations. , 2008, Biophysical journal.

[39]  Marjeta Urh,et al.  HaloTag: a novel protein labeling technology for cell imaging and protein analysis. , 2008, ACS chemical biology.

[40]  Gerhard J Schütz,et al.  Tracking single molecules in the live cell plasma membrane-Do's and Don't's. , 2008, Methods.

[41]  Gaudenz Danuser,et al.  Computational image analysis of cellular dynamics: a case study based on particle tracking. , 2009, Cold Spring Harbor protocols.

[42]  Michael J. Saxton,et al.  SINGLE-PARTICLE TRACKING , 2009 .

[43]  Antoine Triller,et al.  Single‐particle tracking methods for the study of membrane receptors dynamics , 2009, The European journal of neuroscience.

[44]  Yannis Kalaidzidis,et al.  Multiple objects tracking in fluorescence microscopy , 2008, Journal of mathematical biology.

[45]  Nico Stuurman,et al.  Computer Control of Microscopes Using µManager , 2010, Current protocols in molecular biology.

[46]  Klaus Müllen,et al.  Single molecule fluorescence microscopy investigations on heterogeneity of translational diffusion in thin polymer films. , 2011, Physical chemistry chemical physics : PCCP.

[47]  Akihiro Kusumi,et al.  Hierarchical mesoscale domain organization of the plasma membrane. , 2011, Trends in biochemical sciences.