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Anomalous Diffusion in Inverted Variable-Lengthscale Fluorescence Correlation Spectroscopy.


ABSTRACT: Using fluorescence correlation spectroscopy (FCS) to distinguish between different types of diffusion processes is often a perilous undertaking because the analysis of the resulting autocorrelation data is model dependant. Two recently introduced strategies, however, can help move toward a model-independent interpretation of FCS experiments: 1) the obtention of correlation data at different length scales and 2) their inversion to retrieve the mean-squared displacement associated with the process under study. We use computer simulations to examine the signature of several biologically relevant diffusion processes (simple diffusion, continuous-time random walk, caged diffusion, obstructed diffusion, two-state diffusion, and diffusing diffusivity) in variable-length-scale FCS. We show that, when used in concert, length-scale variation and data inversion permit us to identify non-Gaussian processes and, regardless of Gaussianity, to retrieve their mean-squared displacement over several orders of magnitude in time. This makes unbiased discrimination between different classes of diffusion models possible.

SUBMITTER: Stolle MDN 

PROVIDER: S-EPMC6400862 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

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Anomalous Diffusion in Inverted Variable-Lengthscale Fluorescence Correlation Spectroscopy.

Stolle Michael D N MDN   Fradin Cécile C  

Biophysical journal 20190130 5


Using fluorescence correlation spectroscopy (FCS) to distinguish between different types of diffusion processes is often a perilous undertaking because the analysis of the resulting autocorrelation data is model dependant. Two recently introduced strategies, however, can help move toward a model-independent interpretation of FCS experiments: 1) the obtention of correlation data at different length scales and 2) their inversion to retrieve the mean-squared displacement associated with the process  ...[more]

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