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Dive into the research topics where Gillian L. Ryan is active.

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Featured researches published by Gillian L. Ryan.


Biomacromolecules | 2010

Protein Specificity of Charged Sequences in Polyanions and Heparins

A. Basak Kayitmazer; Bonnie Quinn; Kozue Kimura; Gillian L. Ryan; Angela J. Tate; David A. Pink; Paul L. Dubin

Long-range electrostatic interactions are generally assigned a subordinate role in the high-affinity binding of proteins by glycosaminoglycans, the most highly charged biopolyelectrolytes. The discovery of high and low sulfation domains in heparan sulfates, however, suggests selectivity via complementarity of their linear sulfation patterns with protein charge patterns. We examined how charge sequences in anionic/nonionic copolymers affect their binding to a protein with prominent charge anisotropy. Experiments and united-atom Monte Carlo simulations, together with Delphi electrostatic modeling for the protein, confirm strongest binding when polyanion sequences allow for optimization of repulsive and attractive electrostatics. Simulations also importantly identified retention of considerable polyion conformational freedom, even for strong binding. The selective affinity for heparins of high and low charge density found for this protein is consistent with nonspecific binding to distinctly different protein charge domains. These findings suggest a more nuanced view of specificity than previously proposed for heparinoid-binding proteins.


Cytoskeleton | 2012

A review of models of fluctuating protrusion and retraction patterns at the leading edge of motile cells.

Gillian L. Ryan; Dimitrios Vavylonis

A characteristic feature of motile cells as they undergo a change in motile behavior is the development of fluctuating exploratory motions of the leading edge, driven by actin polymerization. We review quantitative models of these protrusion and retraction phenomena. Theoretical studies have been motivated by advances in experimental and computational methods that allow controlled perturbations, single molecule imaging, and analysis of spatiotemporal correlations in microscopic images. To explain oscillations and waves of the leading edge, most theoretical models propose nonlinear interactions and feedback mechanisms among different components of the actin cytoskeleton system. These mechanisms include curvature‐sensing membrane proteins, myosin contraction, and autocatalytic biochemical reaction kinetics. We discuss how the combination of experimental studies with modeling promises to quantify the relative importance of these biochemical and biophysical processes at the leading edge and to evaluate their generality across cell types and extracellular environments.


Molecular Biology of the Cell | 2014

New single-molecule speckle microscopy reveals modification of the retrograde actin flow by focal adhesions at nanometer scales

Sawako Yamashiro; Hiroaki Mizuno; Matthew B. Smith; Gillian L. Ryan; Tai Kiuchi; Dimitrios Vavylonis

This paper introduces a new, easy-to-use method of fluorescence single-molecule speckle microscopy for actin with nanometer-scale accuracy. This new method reveals that actin flows in front of mature focal adhesions (FAs) are fast and biased toward FAs, suggesting that mature FAs are actively engaged in pulling and remodeling the local actin network.


Materials | 2017

Reduced Graphene Oxide on Nickel Foam for Supercapacitor Electrodes

Uma Ramabadran; Gillian L. Ryan; Xuan Zhou; Susan Farhat; Felicia Manciu; Yigang Tong; Ryan Ayler; Graham Garner

The focus of this paper is the investigation of reduced graphene oxide (GO)/nickel foam (RGON) samples for use as supercapacitor electrodes. Nickel foam samples were soaked in a GO suspension and dried before being subjected to two different methods to remove oxygen. Atmospheric pressure annealed (APA) samples were treated with a varying number (10–18) of nitrogen plasma jet scans, where sample temperatures did not exceed 280 °C. Furnace annealed (FA) samples were processed in an atmosphere of hydrogen and argon, at temperatures ranging from 600 °C to 900 °C. Environmental Scanning Electron Microscope (ESEM) data indicated that the carbon to oxygen (C:O) ratio for APA samples was minimized at an intermediate number of plasma scans. Fourier Transform Infrared Spectroscopic (FTIR) and Raman spectroscopic data supported this finding. ESEM analysis from FA samples showed that with increasing temperatures of annealing, GO is transformed to reduced graphene oxide (RGO), with C:O ratios exceeding 35:1. X-ray Photoelectron Spectroscopy (XPS) and X-ray diffraction (XRD) data indicated the formation of RGO with an increasing annealing temperature until 800 °C, when oxygen reincorporation in the surface atomic layers becomes an issue. Supercapacitors, constructed using the FA samples, demonstrated performances that correlated with surface atomic layer optimization of the C:O ratio.


Cytoskeleton | 2017

Cell protrusion and retraction driven by fluctuations in actin polymerization: A two-dimensional model

Gillian L. Ryan; Danielle Holz; Sawako Yamashiro; Daisuke Taniguchi; Dimitrios Vavylonis

Animal cells that spread onto a surface often rely on actin‐rich lamellipodial extensions to execute protrusion. Many cell types recently adhered on a two‐dimensional substrate exhibit protrusion and retraction of their lamellipodia, even though the cell is not translating. Travelling waves of protrusion have also been observed, similar to those observed in crawling cells. These regular patterns of protrusion and retraction allow quantitative analysis for comparison to mathematical models. The periodic fluctuations in leading edge position of XTC cells have been linked to excitable actin dynamics using a one‐dimensional model of actin dynamics, as a function of arc‐length along the cell. In this work we extend this earlier model of actin dynamics into two dimensions (along the arc‐length and radial directions of the cell) and include a model membrane that protrudes and retracts in response to the changing number of free barbed ends of actin filaments near the membrane. We show that if the polymerization rate at the barbed ends changes in response to changes in their local concentration at the leading edge and/or the opposing force from the cell membrane, the model can reproduce the patterns of membrane protrusion and retraction seen in experiment. We investigate both Brownian ratchet and switch‐like force‐velocity relationships between the membrane load forces and actin polymerization rate. The switch‐like polymerization dynamics recover the observed patterns of protrusion and retraction as well as the fluctuations in F‐actin concentration profiles. The model generates predictions for the behavior of cells after local membrane tension perturbations.


Biophysical Journal | 2012

Excitable Actin Dynamics in Lamellipodial Protrusion and Retraction

Gillian L. Ryan; Heather Petroccia; Dimitrios Vavylonis


Cell Structure and Function | 2013

Image Analysis Tools to Quantify Cell Shape and Protein Dynamics near the Leading Edge

Gillian L. Ryan; Dimitrios Vavylonis


Bulletin of the American Physical Society | 2015

Cellular Hokey Pokey: A Coarse-Grained Model of Lamellipodia Protrusion Dynamics Driven by Fluctuations in Actin Polymerization

Gillian L. Ryan; Dimitrios Vavylonis


Bulletin of the American Physical Society | 2015

Latent Heat Recovery Modification from Sodium Acetate Trihydrate due to Structural Changes Caused by Silver Nanoparticles

Gillian L. Ryan; Uma B. Ramabadran; Frederick Garcia


Biophysical Journal | 2012

A Two-Dimensional Model of Leading Edge Protrusion and Retraction Driven by Excitable Actin Dynamics

Gillian L. Ryan; Dimitrios Vavylonis

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Bonnie Quinn

St. Francis Xavier University

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David A. Pink

St. Francis Xavier University

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A. Basak Kayitmazer

University of Massachusetts Amherst

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Felicia Manciu

University of Texas at El Paso

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Paul L. Dubin

University of Massachusetts Amherst

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