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Mary Lou P. Bailey

Publications and source records attributed to Mary Lou P. Bailey.

2 recordsLinked to original sources

The effect of loops on the mean square displacement of Rouse-model chromatin

Many researchers have been encouraged to describe the dynamics of chromosomal loci in chromatin using the classical Rouse model of polymer dynamics by the agreement between the measured mean square displacement (MSD) versus time of fluorescently-labelled loci and the Rouse-model predictions. However, the discovery of intermediate-scale chromatin organization, known as topologically associating domains (TADs), together with the proposed explanation of TADs in terms of chromatin loops and loop extrusion, is at odds with the classical Rouse model, which does not contain loops. Accordingly, we introduce an extended Rouse model that incorporates chromatin loop configurations from loop-extrusion-factor-model simulations. Specifically, we extend the classical Rouse model by modifying the polymer's dynamical matrix to incorporate extra springs that represent loop bases. We also theoretically generalize the friction coefficient matrix so that the Rouse beads with non-uniform friction coefficients are compatible with our Rouse model simulation method. This extended Rouse model allowes us to investigate the impact of loops and loop extrusion on the dynamics of chromatin. We show that loops significantly suppress the averaged MSD of a chromosomal locus, consistent with recent experiments that track fluorescently-labelled chromatin loci in fission yeast [M. L. P. Bailey, I. Surovtsev, J. F. Williams, H. Yan, T. Yuan, S. G. Mochrie, and M. C. King, Mol. Biol. Cell (in press)]. We also find that loops slightly reduce the MSD's stretching exponent from the classical Rouse-model value of 0.5 to a loop-density-dependent value in the 0.45-0.40 range. Remarkably, stretching exponent values in this range have also been reported in recent experiments [S. C. Weber, A. J. Spakowitz, and J. A. Theriot, Phys. Rev. Lett. 104, 238102 (2010) and Bailey et al., Mol. Biol. Cell (in press)].

physics.bio-ph↗

Uncovering diffusive states of the yeast proton pump, Pma1, and how labeling method can change diffusive behavior

We present and analyze video-microscopy-based single-particle-tracking measurements of the budding yeast (Saccharomyces cerevisiae) membrane protein, Pma1, fluorescently-labeled either by direct fusion to the switchable fluorescent protein, mEos3.2, or by a novel, light-touch, labeling scheme, in which a 5 amino acid tag is directly fused to the C-terminus of Pma1, which then binds mEos3.2. The diffusivity distributions of these two populations of single particle tracks differ significantly, demonstrating that labeling method can be an important determinant of diffusive behavior. We also applied perturbation expectation maximization (pEMv2) [Physical Review E 94, 052412 (2016)], which sorts trajectories into the statistically-optimum number of diffusive states. For both TRAP-labeled Pma1 and Pma1-mEos3.2, pEMv2 sorts the tracks into two diffusive states: an essentially immobile state and a more mobile state. However, the mobile fraction of Pma1-mEos3.2 tracks is much smaller (0.1) than the mobile fraction of TRAP-labeled Pma1 tracks (0.5). In addition, the diffusivity of Pma1-mEos3.2's mobile state is several times smaller than the diffusivity of TRAP-labeled Pma1's mobile state. To critically assess pEMv2's performance, we compare the diffusivity and covariance distributions of the experimental pEMv2-sorted populations to corresponding theoretical distributions, assuming that Pma1 displacements realize a Gaussian random process. The experiment-theory comparisons for both the TRAP-labeled Pma1 and Pma1-mEos3.2 reveal good agreement, bolstering the pEMv2 approach.

physics.bio-ph↗