Surface-attached Particles Research Articles

Particulate Projectiles Driven by Cavitation Bubbles.

The removal of surface-attached particles with cavitation bubbles is usually attributed to the jetting or shear stresses when bubbles collapse. In this Letter, we report an unexpected phenomenon that millimeter-sized spherical particles made of heavy metals (e.g., stainless steel), when initially resting on a fixed rigid substrate, are suddenly accelerated like projectiles through the production of nearby laser-induced cavitation bubbles of similar sizes. We show experimentally and theoretically that the motion of a particle with radius R_{p} is determined by the maximum bubble radius R_{b,max}, the initial distance from the laser focus to the center of the particle L_{0}, and the initial azimuth angle φ_{0}. We identify two dominant regimes for the particle's sudden acceleration, namely, the unsteady liquid inertia dominated regime and the bubble contact dominated regime, determined by R_{b,max}R_{p}/L_{0}^{2}. We find the nondimensional maximum vertical displacement of the particle follows the fourth power and the square power scaling laws for respective regimes, which is consistent with the experimental results. Our findings can be applied to nonintrusive particle manipulation from solid substrates in a liquid.

Coupled resonances allow studying the aging of adhesive contacts between a QCM surface and single, micrometer-sized particles

Interparticle contacts and contacts between particles and surfaces are known to change over time. The contact area, the contact stiffness, and the contact strength usually increase as the contact ages. Contact aging is mostly driven by capillary forces, but also by plastic deformation. Making use of acoustic resonators, we have studied the stiffness of contacts between the surface of a quartz crystal microbalance (QCM) and individual, micrometer-sized particles adsorbed to the resonator surface. Studying single particles avoids ensemble-averaging. Central to the analysis is the coupled resonance, occurring when a surface-attached particle together with the link forms a resonator of its own. If the frequency of this second resonator comes close to one of the crystal’s overtones, plots of shifts in resonance bandwidth versus overtone order display a resonance curve. This secondary resonance is caused by the coupling between the particle’s resonance and the main resonance. One can read the frequency of the coupled resonance from this plot. Similarly, resonance curves are observed in plots of frequency and bandwidth versus time, if the contact stiffness varies smoothly with time. Because the coupled resonance is a characteristic feature, it is easily identified even in cases where frequency shifts of some other origin are superimposed onto the data. For the cases studied here, the links stiffened while they dried. Interestingly, the efficiency of coupling between the particle resonance and the main resonance decreased at the same time. This can be explained with an increase in the link’s bending stiffness. The analysis highlights that a QCM experiment amounts to vibrational spectroscopy on surface-attached particles. Among the application examples is the adsorption and drying of a lycopodium spore. Clearly, the technique is also applicable to problems of bioadhesion.

Morphology and Nanomechanical Properties of the T7 Bacteriophage

The T7 bacteriophage contains a linear molecule of double-stranded DNA packaged within a proteinaceous capsid. The capsid is thought to play a mechanoprotective role and to store the energy necessary for DNA injection into host bacterium. In previous melting experiments on T7 particles followed with UV- and CD- spectroscopy two thermal transition steps were detected: one around 65 °C and another around 80 °C. These transitions are probably due to the loosening of the capsid structure and DNA strand separation, respectively. Conceivably, these transitions also influence the capsid's mechanical characteristics. To investigate the effect of temperature on the morphology and nanomechanical properties of the T7 bacteriophage, surface-attached particles were studied with atomic force microscopy and force spectroscopy methods. The experiments were carried out at room temperature, 65 °C and 80 °C. The surface-attached virus particles appeared in the AFM images as spherical objects with a radius of 25-30 nm, a value that correlates with cryo-electron microscopic data. During indentation of the particles we most often observed a force transition containing two subsequent peaks. Conceivaby, the first peak corresponds to the collapse of the upper shell wall, whereas the second peak to the rupture of the lower one. The stiffness of T7 phage wall calculated from the slope of the first transition increased as a function of temperature. In sum, the temperature-dependent changes related to the structural alteration of the T7 capsid's proteins and its DNA result in global changes in the capsid's nanomechanical properties.

Colloidal Dynamics Near a Particle-Covered Surface

How the diffusive dynamics of colloidal spheres changes in the vicinity of a particle-coated surface is of importance for industrial challenges such as fouling and sedimentation as well as for fundamental studies into confinement effects. We addressed this question by studying colloidal dynamics in a partially coated surface layer, using video microscopy. Particle mean squared displacement (MSD) functions were measured as a function of a (local) effective volume fraction (EVF), which was varied by making use of gravity settling. Comparison of MSDs at the bare and coated surfaces for EVF of 0.2-0.4 revealed that at the latter surface the motion amplitudes are strongly reduced, accompanied by a sharp transition from diffusive to nearly caged motion. This clearly indicates that the surface-attached particles cannot be taken into account via volume fraction and that their immobility has a distinct effect. For EVF > 0.45, the caging becomes dominated by the suspended particles, making the dynamics at the bare and coated surfaces similar.

Actin-dependent, retrograde motility of surface-attached beads and aggregating pigment granules in dissociated teleost retinal pigment epithelial cells.

Teleost retinal pigment epithelial (RPE) cells contain pigment granules within apical projections which undergo actin-dependent, bi-directional motility. Dissociated RPE cells in culture attach to the substrate and extend apical projections in a radial array from the central cell body. Pigment granules within projections can be triggered to aggregate or disperse by the presence or absence of 1 mM cAMP. Aminated, fluorescent latex beads attached to the dorsal surface of apical projections and moved in the retrograde direction, towards the cell body. Bead rates on RPE cells with aggregating or fully aggregated pigment granules were 2.2 +/- 0.5 and 2.6 +/- 0.2 microm/min (mean +/- SEM), respectively, similar to rates of aggregating (retrograde) pigment granule movement (2.0 +/- 0.4 microm/min). Bead rates were slightly slower on cells with fully dispersed or dispersing pigment granules (1.5 +/- 0.1 and 1.5 +/- 0.4 microm/min). Movements of surface-attached beads and aggregating pigment granules were closely correlated in the distal portions of apical projections, but were more independent of each other in proximal regions of the projections. The actin disrupting drug, cytochalasin D (CD), reversibly halted retrograde bead movements, suggesting that motility of surface-attached particles is actin-dependent. In contrast, the microtubule depolymerizing drug, nocodazole, had no effect on retrograde bead motility. The similar characteristics and actin-dependence of retrograde bead movements and aggregating pigment granules suggest a correlation between these two processes.

Reactivation of cell surface transport in Reticulomyxa

Granuloreticulosean protists transport particles (e.g., bacteria, algae, and sand grains) along the outer surfaces of their pseudopodia. This cell surface transport plays a vital role in feeding, reproduction, shell construction, and locomotion and can be visualized by the movements of extracellularly adherent polystyrene microspheres (i.e., latex beads). Our videomicroscopic analyses of transport associated with the pseudopodia of Reticulomyxa filosa revealed two distinct types of both intracellular and cell surface transport: (1) saltatory, bidirectional transport of individual or clustered organelles and/or surface-attached particles, and (2) continuous, unidirectional bulk or “resolute” motion of aggregated organelles and/or surface-bound particles. Organelles and surface-attached polystyrene microspheres remained firmly attached to the microtubule cytoskeletons of detergent-extracted pseudopodia. Both saltatory and resolute organelle and surface transport reactivated upon the addition of 0.01–1.0 mM ATP. At 1 mM ATP, the velocities of reactivated saltatory transport were indistinguishable from those observed in vivo. The reactivated transport was microtubule-dependent and was not inhibited by incubation with Ca2+-gelsolin under conditions that abolish rhodamine-phalloidin detection of actin filaments. These findings provide further support that both intracellular organelle and membrane surface transport are mediated by a common mechanism, and establish Reticulomyxa as a unique model system to further study the mechanochemistry of cell surface transport in vitro. Cell Motil. Cytoskeleton 37:139–148, 1997. © 1997 Wiley-Liss Inc.

Reactivation of cell surface transport in Reticulomyxa.

Granuloreticulosean protists transport particles (e.g., bacteria, algae, and sand grains) along the outer surfaces of their pseudopodia. This cell surface transport plays a vital role in feeding, reproduction, shell construction, and locomotion and can be visualized by the movements of extracellularly adherent polystyrene microspheres (i.e., latex beads). Our videomicroscopic analyses of transport associated with the pseudopodia of Reticulomyxa filosa revealed two distinct types of both intracellular and cell surface transport: (1) saltatory, bidirectional transport of individual or clustered organelles and/or surface-attached particles, and (2) continuous, unidirectional bulk or "resolute" motion of aggregated organelles and/or surface-bound particles. Organelles and surface-attached polystyrene microspheres remained firmly attached to the microtubule cytoskeletons of detergent-extracted pseudopodia. Both saltatory and resolute organelle and surface transport reactivated upon the addition of 0.01-1.0 mM ATP. At 1 mM ATP, the velocities of reactivated saltatory transport were indistinguishable from those observed in vivo. The reactivated transport was microtubule-dependent and was not inhibited by incubation with Ca(2+)-gelsolin under conditions that abolish rhodamine-phalloidin detection of actin filaments. These findings provide further support that both intracellular organelle and membrane surface transport are mediated by a common mechanism, and establish Reticulomyxa as a unique model system to further study the mechanochemistry of cell surface transport in vitro.

Molecular mechanism of actin-dependent retrograde flow in lamellipodia of motile cells.

In motile, eukaryotic cells, a variety of cell-associated material (collectively termed here as 'particles') continuously flows, relative to the substratum, from the front to the back of the extreme margin of the cell (termed the 'lamellipodium'). This retrograde particle flow, occurs both over the surface of, and inside the lamellipodium. Force to drive retrograde particle flow in lamellipodia is dependent on actin filaments, but the precise mechanism of force generation, and function of the flow is generally not well understood. Actin filaments themselves, in lamellipodia of most motile cell types studied also flow retrograde relative to the substratum. This actin flow, in Aplysia bag cell neuronal growth cones, is known to be driven by activity of a myosin. In these growth cones, retrograde flow of cell surface-attached particles is coupled to retrograde actin flow. In Aplysia, force from retrograde actin flow may limit certain types of growth cone motility. In other motile cell types, such as keratocytes and fibroblasts, the mechanism of retrograde particle flow and function of retrograde actin flow in lamellipodia is poorly understood. For these cell types, recent data provide a basis for proposing alternative actin-based mechanisms to drive retrograde particle flow in lamellipodia. One mechanism is based on activity of a putative pointed end- directed actin motor, and the other on tension-driven surface lipid flow. Here I will review recent advances that have been made in determining the molecular mechanism of force generation to drive retrograde particle flow relative to the substratum in lamellipodia of motile cells. I will address the function of retrograde actin flow in lamellipodia, and apparent differences between Aplysia and other motile cell types.