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Laurence Salome

Publications and source records attributed to Laurence Salome.

3 recordsLinked to original sources

Probing DNA conformational changes with high temporal resolution by Tethered Particle Motion

The Tethered Particle Motion (TPM) technique informs about conformational changes of DNA molecules, e.g. upon looping or interaction with proteins, by tracking the Brownian motion of a particle probe tethered to a surface by a single DNA molecule and detecting changes of its amplitude of movement. We discuss in this context the time resolution of TPM, which strongly depends on the particle-DNA complex relaxation time, i.e. the characteristic time it takes to explore its configuration space by diffusion. By comparing theory, simulations and experiments, we propose a calibration of TPM at the dynamical level: we analyze how the relaxation time grows with both DNA contour length (from 401 to 2080 base pairs) and particle radius (from 20 to 150~nm). Notably we demonstrate that, for a particle of radius 20~nm or less, the hydrodynamic friction induced by the particle and the surface does not significantly slow down the DNA. This enables us to determine the optimal time resolution of TPM in distinct experimental contexts which can be as short as 20~ms.

cond-mat.soft↗

Comment to the Paper of Michael J. Saxton: "A Biological Interpretation of Transient Anomalous Subdiffusion. I. Qualitative Model"

In a recent paper, Michael J. Saxton proposes to interpret as anomalous diffusion the occurrence of apparent transient sub-diffusive regimes in mean-squared displacements (MSD) plots, calculated from experimental trajectories of molecules diffusing in living cells, acquired by Single Particle (or Molecule) Tracking techniques (SPT or SMT). In this Comment, without questioning the existence of sub-diffusive behaviors, which certainly play a key role in numbers of mechanisms in living systems, we point out that the data used by J.M. Saxton can as well be fitted by a simple law, resulting from confined diffusion at short times, with a slower free diffusion superimposed at larger times. When visualizing MSD plots, the transition from short-term diffusion confined in domains of size L, to slower, longer-term free diffusion, can be confused with anomalous diffusion over several orders of magnitude of time.

q-bio.SC↗

Quantification and Correction of Systematic Errors Due to Detector Time-Averaging in Single-Molecule Tracking Experiments

Single-molecule tracking is a powerful way to look at the dynamic organization of plasma membranes. However, there are some limitations to its use. For example, it was recently observed, using numerical simulation, that time-averaging effects inherent to the exposure time of detectors are likely to bias the apparent motion of molecules confined in microdomains. Here, we solve this apparently limiting issue analytically. We explore this phenomenon by calculating its effects on the observed diffusion coefficients and domain sizes. We demonstrate that the real parameters can be easily recovered from the measured apparent ones. Interestingly, we find that single-molecule tracking can be used to explore events occurring at a timescale smaller than the exposure time.

q-bio.QM↗