Eric R. Dufresne

Mechanotransduction and extracellular matrix homeostasis

Soft connective tissues at steady state are dynamic; resident cells continually read environmental cues and respond to them to promote homeostasis, including maintenance of the mechanical properties of the extracellular matrix (ECM) that are fundamental to cellular and tissue health. The mechanosensing process involves assessment of the mechanics of the ECM by the cells through integrins and the actomyosin cytoskeleton, and is followed by a mechanoregulation process, which includes the deposition, rearrangement or removal of the ECM to maintain overall form and function. Progress towards understanding the molecular, cellular and tissue-level effects that promote mechanical homeostasis has helped to identify key questions for future research.

Optical tweezer arrays and optical substrates created with diffractive optics

We describe a simple method for creating multiple optical tweezers from a single laser beam using diffractive optical elements. As a demonstration of this technique, we have implemented a 4×4 square array of optical tweezers—the hexadeca tweezer. Not only will diffractively generated optical tweezers facilitate many new experiments in pure and applied physics, but they also will be useful for fabricating nanocomposite materials and devices, including photonic bandgap materials and optical circuit elements.

Computer-generated holographic optical tweezer arrays

Holographic techniques significantly extend the capabilities of laser tweezing, making possible extended trapping patterns for manipulating large numbers of particles and volumes of soft matter. We describe practical methods for creating arbitrary configurations of optical tweezers using computer-generated diffractive optical elements. While the discussion focuses on ways to create planar arrays of identical tweezers, the approach can be generalized to three-dimensional arrangements of heterogeneous tweezers and extended trapping patterns.

Membrane Tension Maintains Cell Polarity by Confining Signals to the Leading Edge during Neutrophil Migration

Little is known about how neutrophils and other cells establish a single zone of actin assembly during migration. A widespread assumption is that the leading edge prevents formation of additional fronts by generating long-range diffusible inhibitors or by sequestering essential polarity components. We use morphological perturbations, cell-severing experiments, and computational simulations to show that diffusion-based mechanisms are not sufficient for long-range inhibition by the pseudopod. Instead, plasma membrane tension could serve as a long-range inhibitor in neutrophils. We find that membrane tension doubles during leading-edge protrusion, and increasing tension is sufficient for long-range inhibition of actin assembly and Rac activation. Furthermore, reducing membrane tension causes uniform actin assembly. We suggest that tension, rather than diffusible molecules generated or sequestered at the leading edge, is the dominant source of long-range inhibition that constrains the spread of the existing front and prevents the formation of secondary fronts.

Structure, function, and self-assembly of single network gyroid (I4132) photonic crystals in butterfly wing scales

Complex three-dimensional biophotonic nanostructures produce the vivid structural colors of many butterfly wing scales, but their exact nanoscale organization is uncertain. We used small angle X-ray scattering (SAXS) on single scales to characterize the 3D photonic nanostructures of five butterfly species from two families (Papilionidae, Lycaenidae). We identify these chitin and air nanostructures as single network gyroid (I4132) photonic crystals. We describe their optical function from SAXS data and photonic band-gap modeling. Butterflies apparently grow these gyroid nanostructures by exploiting the self-organizing physical dynamics of biological lipid-bilayer membranes. These butterfly photonic nanostructures initially develop within scale cells as a core-shell double gyroid (Ia3d), as seen in block-copolymer systems, with a pentacontinuous volume comprised of extracellular space, cell plasma membrane, cellular cytoplasm, smooth endoplasmic reticulum (SER) membrane, and intra-SER lumen. This double gyroid nanostructure is subsequently transformed into a single gyroid network through the deposition of chitin in the extracellular space and the degeneration of the rest of the cell. The butterflies develop the thermodynamically favored double gyroid precursors as a route to the optically more efficient single gyroid nanostructures. Current approaches to photonic crystal engineering also aim to produce single gyroid motifs. The biologically derived photonic nanostructures characterized here may offer a convenient template for producing optical devices based on biomimicry or direct dielectric infiltration.

The Bacterial Cytoplasm Has Glass-like Properties and Is Fluidized by Metabolic Activity

The physical nature of the bacterial cytoplasm is poorly understood even though it determines cytoplasmic dynamics and hence cellular physiology and behavior. Through single-particle tracking of protein filaments, plasmids, storage granules, and foreign particles of different sizes, we find that the bacterial cytoplasm displays properties that are characteristic of glass-forming liquids and changes from liquid-like to solid-like in a component size-dependent fashion. As a result, the motion of cytoplasmic components becomes disproportionally constrained with increasing size. Remarkably, cellular metabolism fluidizes the cytoplasm, allowing larger components to escape their local environment and explore larger regions of the cytoplasm. Consequently, cytoplasmic fluidity and dynamics dramatically change as cells shift between metabolically active and dormant states in response to fluctuating environments. Our findings provide insight into bacterial dormancy and have broad implications to our understanding of bacterial physiology, as the glassy behavior of the cytoplasm impacts all intracellular processes involving large components.

Biomimetic Isotropic Nanostructures for Structural Coloration

The self-assembly of films that mimic color-producing nanostructures in bird feathers is described. These structures are isotropic and have a characteristic length-scale comparable to the wavelength of visible light. Structural colors are produced when wavelength-independent scattering is suppressed by limiting the optical path length through geometry or absorption.

High-Yield Synthesis of Monodisperse Dumbbell-Shaped Polymer Nanoparticles

We describe a method for producing highly monodisperse dumbbell-shaped polymer nanoparticles with dimensions on the order of a few hundred nanometers in extremely high yields. Our technique is based on seeded polymerization, where suspended core-shell particles (linear polystyrene core with polystyrene-co-trimethoxysilylpropylacrylate shell) are used as seeds. When an aqueous suspension of seed particles is mixed with monomer solution, the core-shell particles display dramatic changes in their morphology. Subsequent heating drives the polymerization of monomer, resulting in the formation of dumbbell-shaped particles. The relative sizes of the two lobes can be controlled by varying the relative volume of the monomer with respect to the seed particle. These particles are well-suited for future studies of the assembly of photonic crystals of anisotropic particles.

How Noniridescent Colors Are Generated by Quasi‐ordered Structures of Bird Feathers

We investigate the mechanism of structural coloration by quasi-ordered nanostructures in bird feather barbs. Small-angle X-ray scattering (SAXS) data reveal the structures are isotropic and have short-range order on length scales comparable to optical wavelengths. We perform angle-resolved reflection and scattering spectrometry to fully characterize the colors under directional and omni-directional illumination of white light. Under directional lighting, the colors change with the angle between the directions of illumination and observation. The angular dispersion of the primary peaks in the scattering/reflection spectra can be well explained by constructive interference of light that is scattered only once in the quasi-ordered structures. Using the Fourier power spectra of structure from the SAXS data we calculate optical scattering spectra and explain why the light scattering peak is the highest in the backscattering direction. Under omni-directional lighting, colors from the quasi-ordered structures are invariant with the viewing angle. The non-iridescent coloration results from the isotropic nature of structures instead of strong backscattering.

Universal deformation of soft substrates near a contact line and the direct measurement of solid surface stresses

Droplets deform soft substrates near their contact lines. Using confocal microscopy, we measure the deformation of silicone gel substrates due to glycerol and fluorinated-oil droplets for a range of droplet radii and substrate thicknesses. For all droplets, the substrate deformation takes a universal shape close to the contact line that depends on liquid composition, but is independent of droplet size and substrate thickness. This shape is determined by a balance of interfacial tensions at the contact line and provides a novel method for direct determination of the surface stresses of soft substrates. Moreover, we measure the change in contact angle with droplet radius and show that Youngs law fails for small droplets when their radii approach an elastocapillary length scale. For larger droplets the macroscopic contact angle is constant, consistent with Youngs law.