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Biomedical subjects

Hung-Jen Wu

Publications and source records attributed to Hung-Jen Wu.

6 recordsLinked to original sources

Diffusing colloidal probes of protein and synthetic macromolecule interactions.

A new approach is described for measuring kT and nanometer scale protein-protein and protein-synthetic macromolecule interactions. The utility of this method is demonstrated by measuring interactions of bovine serum albumin (BSA) and copolymers with exposed polyethyleneoxide (PEO) moieties adsorbed to hydrophobically modified colloids and surfaces. Total internal reflection and video microscopy are used to track three-dimensional trajectories of many single diffusing colloids that are analyzed to yield interaction potentials, mean-square displacements, and colloid-surface association lifetimes. A criterion is developed to identify colloids as being levitated, associated, or deposited based on energetic, spatial, statistical, and temporal information. Whereas levitation and deposition occur for strongly repulsive or attractive potentials, association is exponentially sensitive to weak interactions influenced by adsorbed layer architectures and surface heterogeneity. Systematic experiments reveal how BSA orientation and PEO molecular weight produce adsorbed layers that either conceal or expose substrate heterogeneities to generate a continuum of colloid-surface association lifetimes. These measurements provide simultaneous access to a broad range of information that consistently indicates purely repulsive BSA and PEO interactions and a role for surface heterogeneity in colloid-surface association. The demonstrated capability to measure nonspecific protein interactions provides a basis for future measurements of specific protein interactions.

Colloids↗

Mapping patterned potential energy landscapes with diffusing colloidal probes.

We report a new method for mapping patterned surfaces based on monitoring the interactions of freely diffusing colloidal probes with pattern features to generate measured potential energy landscapes. Evanescent wave scattering and video microscopy are used to track 3D center positions of nominal 2 microm silica colloids as they diffuse over 5-20-nm-thick patterned gold films. An analysis of ensemble-averaged particle height histograms on different pattern features using Boltzmann's equation produces local electrostatic and van der Waals potentials in good agreement with independent measurements and predictions. Absolute separation is obtained from theoretical fits to measured potential-energy profiles and direct measurement by depositing silica colloids onto gold surfaces via electrophoretic deposition. As colloidal probe and pattern feature dimensions become comparable, potential energy profiles suffer some distortion due to the increased probability of probes sampling pattern feature edges. An analysis of interfacial colloidal probe diffusion in conjunction with potential energy measurements demonstrates a consistent interpretation of dissipative and conservative forces in these measurements. Future extensions of this work should produce similar approaches for interrogating physical, chemical, and biomolecular heterogeneous/patterned surfaces and structures with diffusing colloidal probes.

Colloids↗

Phosphatized polar lobe-forming embryos from the Precambrian of southwest China.

In developing embryos of some extant spiralian animals, polar lobe formation is one of the symmetry-breaking mechanisms for segregation of maternal cytoplasmic substances to certain blastomeres and not others. Polar lobe formation leads to unique early cleavage morphologies that include trilobed, J-shaped, and five-lobed structures. Fossil embryos similar to modern lobeforming embryos are recognized from the Precambrian Doushantuo Formation phosphates, Weng'an, Guizhou Province, China. These embryos are abundant and form a developmental sequence comparable to different developing stages observed in lobe-forming embryos of extant spiralians. These data imply that lobe formation is an evolutionarily ancient process of embryonic specification.

Animals↗

Measurement and interpretation of particle-particle and particle-wall interactions in levitated colloidal ensembles.

This paper reports measurements of particle-wall and particle-particle interactions in levitated colloidal ensembles using integrated total internal reflection microscopy (TIRM) and video microscopy (VM) techniques. In levitated colloidal ensembles with area fractions of phiA = 0.03-0.25, ensemble TIRM measured height distribution functions are used to interpret particle-wall interactions, and VM measured pair distribution functions are used to interpret particle-particle interactions using inverse Ornstein-Zernike (OZ) and three-dimensional inverse Monte Carlo (MC) analyses. An inconsistent finding is the observation of an anomalous long-range particle-particle attraction and recovery of the expected Derjaguin-Landau-Verwey-Overbeek (DLVO) particle-wall interactions for all concentrations examined. Because particle-wall and particle-particle potentials are expected to be consistent in several respects, the analytical and experimental methods employed in this investigation are examined for possible sources of error. Comparison of inverse OZ and three-dimensional inverse MC analyses are used to address uncertainties related to dimensionality, effects of particle concentration, and assumptions of the OZ theory and closure relations. The possible influence of charge heterogeneity and particle size polydispersity on measured distribution functions is discussed with regard to inconsistent particle-wall and particle-particle potentials. Ultimately, achieving a consistent understanding of particle-wall and particle-particle interactions in interfacial and confined colloidal systems is essential to numerous complex fluid and advanced material technologies.

Journal Article↗

Direct measurement of single and ensemble average particle-surface potential energy profiles.

This work involves the development of a novel technique that integrates total internal reflection and video microscopy methods to simultaneously measure single particle and ensemble average particle-surface interactions. For the 2 mum silica colloids and glass coverslip used in this study, particle size polydispersity is found to be a dominant factor in determining the distribution of single particle profiles about ensemble average profiles. In conjunction with this observation, chemical and physical nonuniformity are not evident in any of our measurements even with sensitivity to interactions on the order of kT. One advantage of using ensemble averaging in conjunction with time averaging is the ability to dramatically decrease the time required to measure average particle-wall interactions which scales inversely with interfacial particle concentration. A number of experimental issues are addressed in the development of this technique including (1) combining single particle distribution functions, (2) statistical sampling of distribution functions using both time and ensemble averaging, and (3) correcting overlapping scattering signals between adjacent particles. The capabilities of the ensemble averaging technique are also demonstrated to provide unique measurements of particle-surface interactions in metastable systems by selecting only height excursions of levitated particles when calculating potentials. Ultimately, this new technique provides several important advantages over single particle measurements, which provides a foundation for measuring interactions in increasingly complex interfacial systems.

Journal Article↗

Specific ion-dependent attraction and phase behavior of polymer-coated colloids.

This paper presents results demonstrating the role of temperature and specific ions in mediating attraction between polymer-coated colloids and determining their equilibrium phase behavior. In particular, theoretical predictions of continuum van der Waals attraction between poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO)-coated polystyrene colloids are used to explain measured temperature and specific ion-dependent fluid-gel transitions in dispersions of these particles. Building on previous studies of PEO-PPO-PEO-coated polystyrene colloids dispersed in aqueous NaCl media, this work reports rheologically measured fluid-gel transitions as a function of temperature and NaCl/MgSO4 composition. Adhesive-sphere predictions of percolation thresholds are fit to measured fluid-gel data by allowing the adsorbed copolymer layer thickness as a single adjustable parameter. This allows the attraction between the PEO-PPO-PEO layers to be interpreted as a function of temperature and NaCl/MgSO4 composition. Quantitative predictions of a polymeric van der Waals attraction associated with the layer collapse in diminishing solvent conditions provides a simple mechanism for explaining the measured fluid-gel data as a dynamic percolation transition. Ultimately, this work identifies the importance of continuum polymeric van der Waals attraction for explaining specific ion-dependent phenomena.

Journal Article↗