4.6 Article

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

期刊

PLOS ONE
卷 8, 期 5, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0064287

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资金

  1. Engineering and Physical Sciences Research Council (EPSRC)
  2. Studienstiftung des deutschen Volkes
  3. Horserace Betting Levy Board (HBLB) scholarship
  4. Medical Research Council (MRC)
  5. BBSRC [BB/H021930/1] Funding Source: UKRI
  6. MRC [G1000133, G0901545, MC_UU_12010/4] Funding Source: UKRI
  7. Biotechnology and Biological Sciences Research Council [BB/H021930/1] Funding Source: researchfish
  8. Medical Research Council [G1000133, MC_UU_12010/4, G0901545] Funding Source: researchfish

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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-beta-cyclodextrin and latrunculin B.

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