Application of conducting polymer electrodes in cell impedance sensing

Research in label free methods for biological analysis has brought interesting developments. Cell impedance spectroscopy has been one of the promising outcomes. It allows the measurement of cell proliferation and motility whereby it is possible to study wound healing and cell behavior in vitro. This thesis presents the progress towards an 8-well impedance measurement setup that uses conducting polymers as electrode material in cell impedance spectroscopy. A step by step fabrication of devices with PEDOT:PSS electrodes is described along with the hardware and software, developed and integrated, to perform impedance measurements of cell cultures. Electrochemical analysis was performed for PEDOT:PSS and Au electrodes to compare the two materials for use in cell impedance spectroscopy. PEDOT:PSS electrodes showed lower interfacial impedance and reach electrochemical equilibrium faster than Au electrodes. It was observed through electrochemical impedance analysis that the lower interfacial impedance is due to the low charge transfer resistance of PEDOT:PSS. MDCK cell proliferation experiments were performed using both types of electrode materials to provide a comparative study. The impedance measurement results showed differences between the two materials that led to a different kind of electrical model for the changes measured due to cell proliferation. Curve fitting results to the electrical model provided an understanding of the cell-substrate interactions and the capabilities of cell impedance spectroscopy. The application of cell impedance spectroscopy to human embryonic stem cells was also explored. The impedance changes of pluripotent stem cells during differentiation to trophoblasts were measured and analyzed. Analysis of changes to the phase values in the frequency spectrum show that by measuring the frequency where the phase is minimum, it is possible to distinguish between the two cell types. It provides a new method of using cell impedance spectroscopy to study stem cells behavior in real time and help researchers in the maintaining of stem cell cultures in the lab. Another new application of cell impedance spectroscopy to determine cell types based on the flexibility of the cytoskeleton was also explored. Some preliminary data is presented in the last chapter.

Symmetry reduction and shape effects in concave chiral plasmonic structures

Chiral metamaterials have shown a number of interesting properties which result from the interaction of the chiral near-field they produce with light and matter. We investigate the influence of structural imperfections on the plasmonic properties of a chiral gold “gammadion”, using electron energy loss spectroscopy to directly inform simulations of realistic, imperfect structures. Unlike structures of simple convex geometry, the lowest energy modes of the ideal concave gammadion have a quadrupole and dipole character, with the mode energies determined by the nature of electrostatic coupling between the gammadion arms. These modes are strongly affected by structural imperfections that are inherent to the material properties and lithographic patterning. Even subwavelength-scale imperfections reduce the symmetry, lift mode degeneracies convert dark modes into bright ones and significantly alter the mode energy, its near-field strength, and chirality. Such effects will be common to a number of multitipped concave structures currently being investigated for the chiral fields they support

Active chiral plasmonics: flexoelectric control of nanoscale chirality

The ability to electrically control the optical properties of metamaterials is an essential capability required for technological innovation. The creation of dynamic electrically tuneable metamaterials in the visible and near IR region are important for a range of imaging and fibre optic technologies. However current approaches require complex nanofabrication processes which are incompatible for low cost device production. Here, we report a novel simple approach for electrical control of optical properties which utilises a flexoelectric dielectric element to electromechanically manipulate the form factor of a chiral nanostructure. By altering the dimensions of the chiral nanostructure, we allow the polarisation properties of light to be electrically controlled. The flexoelectric element is part of a composite metafilm that is templated on to a nanostructured polymer substrate. Since the flexoelectric element does not require in situ high temperature annealing it can be readily combined with polymer‐based substrates produced by high throughput methods. This is not the case for piezoelectric elements, routinely used in microelectromechanical (MEM) devices which require high temperature processing. Consequently, combining amorphous flexoelectric dielectric and low‐cost polymer‐based materials provides a route to the high throughput production of electrically responsive disposable metadevices

Roles of superchirality and interference in chiral plasmonic biodetection

Chiral plasmonic nanostructures enable ≤pg detection and characterization of biomaterials. The sensing capabilities are associated with the chiral asymmetry of the near fields, which locally can be greater than equivalent circularly polarized light, a property referred to as superchirality. However, sensing abilities do not simply scale with the magnitude of superchirality. We show that chiral molecular sensing is correlated to the thickness of a nanostructure. This observation is reconciled with a previously unconsidered interference mechanism for the sensing phenomenon. It involves the “dissipation” of optical chirality into chiral material currents through the interference of fields generated by two spatially separated chiral modes. The presence of a chiral dielectric causes an asymmetric change in the phase difference, resulting in asymmetric changes to chiroptical properties. Thus, designing a chiral plasmonic sensor requires engineering a substrate that can sustain both superchiral fields and an interference effect

Biomacromolecular charge chirality detected using chiral plasmonic nanostructures

The charge distributions of solvent exposed surfaces of complex biomolecules such has proteins are unique fingerprints. The chirality of these charge distributions result in stereo-specific electrostatic interactions which help define how proteins interact with each other, contributing to specificity in protein – protein interactions. Thus it is a key concept in understanding chemical processes in biology. There is currently no known spectroscopic phenomenon that allows rapid characterisation of chiral surface charge distributions. We show that this essential property that is currently “invisible” to optical spectroscopy, can be detected by monitoring asymmetries in the chiroptical response of protein-plasmonic nanostructure complexes. The unique capabilities of the phenomenon are utilised to discriminate between a structurally homologous series of proteins, type II dehydroquinase (DHQase) derived from different organisms. The proteins are indistinguishable with conventional structurally sensitive spectroscopy (i.e. circular dichroism). We show that discrimination between proteins can be achieved by detecting differences in chiral surface charge distributions. The phenomenon is explained with a simple model whereby the chiroptical properties of the plasmonic structures are perturbed by the induction of an enantiomeric mirror image charge distribution of the protein in the metal. This new phenomenon has broad impact, it is a powerful analytical tool for discriminating between structurally homologous biomaterials, but will also provide information relevant to macromolecular interactions

Biomacromolecular stereostructure mediates mode hybridization in chiral plasmonic nanostructures

The refractive index sensitivity of plasmonic fields has been exploited for over 20 years in analytical technologies. While this sensitivity can be used to achieve attomole detection levels, they are in essence binary measurements that sense the presence/absence of a predetermined analyte. Using plasmonic fields, not to sense effective refractive indices but to provide more “granular” information about the structural characteristics of a medium, provides a more information rich output, which affords opportunities to create new powerful and flexible sensing technologies not limited by the need to synthesize chemical recognition elements. Here we report a new plasmonic phenomenon that is sensitive to the biomacromolecular structure without relying on measuring effective refractive indices. Chiral biomaterials mediate the hybridization of electric and magnetic modes of a chiral solid-inverse plasmonic structure, resulting in a measurable change in both reflectivity and chiroptical properties. The phenomenon originates from the electric-dipole–magnetic-dipole response of the biomaterial and is hence sensitive to biomacromolecular secondary structure providing unique fingerprints of α-helical, β-sheet, and disordered motifs. The phenomenon can be observed for subchiral plasmonic fields (i.e., fields with a lower chiral asymmetry than circularly polarized light) hence lifting constraints to engineer structures that produce fields with enhanced chirality, thus providing greater flexibility in nanostructure design. To demonstrate the efficacy of the phenomenon, we have detected and characterized picogram quantities of simple model helical biopolymers and more complex real proteins

Attomole enantiomeric discrimination of small molecules using an achiral SERS reporter and chiral plasmonics

Biologically important molecules span a size range from very large biomacromolecules, such as proteins to small metabolite molecules. Consequently, spectroscopic techniques which can detect and characterize the structure of inherently chiral biomolecules over this range of scale at the femtomole level are necessary to develop novel biosensing and diagnostic technologies. Nanophotonic platforms uniquely enable chirally sensitive structural characterisation of biomacromolecules at this ultrasensitive level. However, they are less successful at achieving the same level of sensitivity for small chiral molecules, with less than nanomole typical. This poorer performance can be attributed to the optical response of the platform being sensitive to a much larger volume of the near field than is occupied by the small molecule. Here we show that by combining chiral plasmonic metasurfaces with Raman reporters, which can detect changes in electromagnetic environment at molecular dimensions, chiral discrimination can be achieved for attomole quantities of a small molecule, the amino acid cysteine. The signal-to-noise, and hence ultimate sensitivity, of the measurement can be further improved by combining the metasurfaces with gold achiral nanoparticles. This indirect enantiomeric detection is 9 orders of magnitude more sensitive than strategies relying on monitoring the Raman response of target chiral molecules directly. Given the generic nature of the phenomenon,this study provides a framework for developing novel technologies for detecting a broad spectrum of small biomolecules, which would be useful tools in the field of metabolomics

Chiral plasmonic fields probe structural order of biointerfaces

The structural order of biopolymers, such as proteins, at interfaces defines the physical and chemical interactions of biological systems with their surroundings and is hence a critical parameter in a range of biological problems. Known spectroscopic methods for routine rapid monitoring of structural order in biolayers are generally only applied to model single-component systems that possess a spectral fingerprint which is highly sensitive to orientation. This spectroscopic behavior is not a generic property and may require the addition of a label. Importantly, such techniques cannot readily be applied to real multicomponent biolayers, have ill-defined or unknown compositions, and have complex spectroscopic signatures with many overlapping bands. Here, we demonstrate the sensitivity of plasmonic fields with enhanced chirality, a property referred to as superchirality, to global orientational order within both simple model and “real” complex protein layers. The sensitivity to structural order is derived from the capability of superchiral fields to detect the anisotropic nature of electric dipole–magnetic dipole response of the layer; this is validated by numerical simulations. As a model study, the evolution of orientational order with increasing surface density in layers of the antibody immunoglobulin G was monitored. As an exemplar of greater complexity, superchiral fields are demonstrated, without knowledge of exact composition, to be able to monitor how qualitative changes in composition alter the structural order of protein layers formed from blood serum, thereby establishing the efficacy of the phenomenon as a tool for studying complex biological interfaces

Probing specificity of protein-protein interactions with chiral plasmonic nanostructures

Protein–protein interactions (PPIs) play a pivotal role in many biological processes. Discriminating functionally important well-defined protein–protein complexes formed by specific interactions from random aggregates produced by nonspecific interactions is therefore a critical capability. While there are many techniques which enable rapid screening of binding affinities in PPIs, there is no generic spectroscopic phenomenon which provides rapid characterization of the structure of protein–protein complexes. In this study we show that chiral plasmonic fields probe the structural order and hence the level of PPI specificity in a model antibody–antigen system. Using surface-immobilized Fab′ fragments of polyclonal rabbit IgG antibodies with high specificity for bovine serum albumin (BSA), we show that chiral plasmonic fields can discriminate between a structurally anisotropic ensemble of BSA-Fab′ complexes and random ovalbumin (OVA)-Fab′ aggregates, demonstrating their potential as the basis of a useful proteomic technology for the initial rapid high-throughput screening of PPIs

Detecting antibody–antigen interactions with chiral plasmons: factors influencing chiral plasmonic sensing

Chiral near fields possessing enhanced asymmetry (superchirality), created by the interaction of light with (chiral) nanostructures, potentially provide a route to novel sensing and metrology technologies for biophysical applications. However, the mechanisms by which these near fields lead to the detection of chiral media is still poorly understood. Using a combination of numerical modeling and experimental measurements on an antibody–antigen exemplar system, important factors that influence the efficacy of chiral sensing are illustrated. It is demonstrated that localized and lattice chiral resonances display enantiomeric sensitivity. However, only the localized resonances show a strong dependency on the structure of the chiral media detected. This can be attributed to the ability of birefringent chiral layers to strongly modify the properties of near fields by acting as a sink/source of optical chirality, and hence alter inductive coupling between nanostructure elements. In addition, it is highlighted that surface morphology/defects may amplify sensing capabilities of localized chiral plasmonic modes by mediating inductive coupling