Plasmonic effects upon optical trapping of metal nanoparticles

Optical trapping of metal nanoparticles investigates phenomena at the interface of plasmonics and optical micromanipulation. This thesis combines ideas of optical properties of metals originating from solid state physics with force mechanism resulting from optical trapping. We explore the influence of the particle plasmon resonance of gold and silver nanospheres on their trapping properties. We aspire to predict the force mechanisms of resonant metal particles with sizes in the Mie regime, beyond the Rayleigh limit. Optical trapping of metal nanoparticles is still considered difficult, yet it provides an excellent tool to investigate their plasmonic properties away from any interface and offers opportunities to investigate interaction processes between light and nanoparticles. Due to their intrinsic plasmon resonance, metal nanoparticles show intriguing optical responses upon interaction with laser light. These differ greatly from the well-known bulk properties of the same material. A given metal nanoparticle may either be attracted or repelled by laser light, only depending on the wavelength of the latter. The optical forces acting on the particle depend directly on its polarisability and scattering cross section. These parameters vary drastically around the plasmon resonance and thus not only change the magnitude but also the direction and entire nature of the acting forces. We distinguish between red-detuned and blue-detuned trapping, that is using a trapping wavelength shorter or longer than the plasmon resonance of the particle. So far optical trapping of metal nanoparticles has focussed on a wavelength regime far from the particle’s resonance in the infrared. We experiment with laser wavelengths close to the plasmon resonance and expand the knowledge of metal nanoparticle trapping available to date. Existing theoretical models are put to the test when we compare these with our real experimental situations

Holographic aberration correction: optimising the stiffness of an optical trap deep in the sample

We investigate the effects of 1st order spherical aberration and defocus upon the stiffness of an optical trap tens of μm into the sample. We control both these aberrations with a spatial light modulator. The key to maintain optimum trap stiffness over a range of depths is a specific non-trivial combination of defocus and axial objective position. This optimisation increases the trap stiffness by up to a factor of 3 and allows trapping of 1μm polystyrene beads up to 50μm deep in the sample.<p></p&gt

Probing Ligand-Receptor Interaction in Living Cells Using Force Measurements With Optical Tweezers

This work probes the binding kinetics of COOH-terminus of Clostridium perfringens enterotoxin (c-CPE) and claudin expressing MCF-7 cells using force spectroscopy with optical tweezers. c-CPE is of high biomedical interest due to its ability to specifically bind to claudin with high affinity as well as reversibly disrupt tight junctions whilst maintaining cell viability. We observed single-step rupture events between silica particles functionalized with c-CPE and MCF-7 cells. Extensive calibration of the optical tweezers’ trap stiffness and displacement of the particle from trap center extracted a probable bond rupture force of ˜ 18 pN. The probability of rupture events with c-CPE functionalized silica particles increased by 50% compared to unfunctionalized particles. Additionally, rupture events were not observed when probing cells not expressing claudin with c-CPE coated particles. Overall, this work demonstrates that optical tweezers are invaluable tools to probe ligand-receptor interactions and their potential to study dynamic molecular events in drug-binding scenarios

Optical vortex trap for resonant confinement of metal nanoparticles

The confinement and controlled movement of metal nanoparticles and nanorods is an emergent area within optical micromanipulation. In this letter we experimentally realise a novel trapping geometry near the plasmon resonance using an annular light field possessing a helical phasefront that confines the nanoparticle to the vortex core (dark) region. We interpret our data with a theoretical framework based upon the Maxwell stress tensor formulation to elucidate the total forces upon nanometric particles near the particle plasmon resonance. Rotation of the particle due to orbital angular momentum transfer is observed. This geometry may have several advantages for advanced manipulation of metal nanoparticles

Optically trapped bacteria pairs reveal discrete motile response to control aggregation upon cell–cell approach

Aggregation of bacteria plays a key role in the formation of many biofilms. The critical first step is cell–cell approach, and yet the ability of bacteria to control the likelihood of aggregation during this primary phase is unknown. Here, we use optical tweezers to measure the force between isolated Bacillus subtilis cells during approach. As we move the bacteria towards each other, cell motility (bacterial swimming) initiates the generation of repulsive forces at bacterial separations of ~3 μm. Moreover, the motile response displays spatial sensitivity with greater cell–cell repulsion evident as inter-bacterial distances decrease. To examine the environmental influence on the inter-bacterial forces, we perform the experiment with bacteria suspended in Tryptic Soy Broth, NaCl solution and deionised water. Our experiments demonstrate that repulsive forces are strongest in systems that inhibit biofilm formation (Tryptic Soy Broth), while attractive forces are weak and rare, even in systems where biofilms develop (NaCl solution). These results reveal that bacteria are able to control the likelihood of aggregation during the approach phase through a discretely modulated motile response. Clearly, the force-generating motility we observe during approach promotes biofilm prevention, rather than biofilm formation

Single-molecule FRET dynamics of molecular motors in an ABEL Trap

Single-molecule F\"orster resonance energy transfer (smFRET) of molecular motors provides transformative insights into their dynamics and conformational changes both at high temporal and spatial resolution simultaneously. However, a key challenge of such FRET investigations is to observe a molecule in action for long enough without restricting its natural function. The Anti-Brownian ELectrokinetic Trap (ABEL trap) sets out to combine smFRET with molecular confinement to enable observation times of up to several seconds while removing any requirement of tethered surface attachment of the molecule in question. In addition, the ABEL trap's inherent ability to selectively capture FRET active molecules accelerates the data acquisition process. Here we exemplify the capabilities of the ABEL trap in performing extended timescale smFRET measurements on the molecular motor Rep, which is crucial for removing protein blocks ahead of the advancing DNA replication machinery and for restarting stalled DNA replication. We are able to monitor single Rep molecules up to 6 s with 1 ms time resolution capturing multiple conformational switching events during the observation time. Here we provide a step-by-step guide for the rational design, construction and implementation of the ABEL trap for smFRET detection of Rep in vitro. We include details of how to model the electric potential at the trap site and use Hidden Markov analysis of the smFRET trajectories

Plasmonic effects upon optical trapping of metal nanoparticles

Optical trapping of metal nanoparticles investigates phenomena at the interface of plasmonics and optical micromanipulation. This thesis combines ideas of optical properties of metals originating from solid state physics with force mechanism resulting from optical trapping. We explore the influence of the particle plasmon resonance of gold and silver nanospheres on their trapping properties. We aspire to predict the force mechanisms of resonant metal particles with sizes in the Mie regime, beyond the Rayleigh limit. Optical trapping of metal nanoparticles is still considered difficult, yet it provides an excellent tool to investigate their plasmonic properties away from any interface and offers opportunities to investigate interaction processes between light and nanoparticles. Due to their intrinsic plasmon resonance, metal nanoparticles show intriguing optical responses upon interaction with laser light. These differ greatly from the well-known bulk properties of the same material. A given metal nanoparticle may either be attracted or repelled by laser light, only depending on the wavelength of the latter. The optical forces acting on the particle depend directly on its polarisability and scattering cross section. These parameters vary drastically around the plasmon resonance and thus not only change the magnitude but also the direction and entire nature of the acting forces. We distinguish between red-detuned and blue-detuned trapping, that is using a trapping wavelength shorter or longer than the plasmon resonance of the particle. So far optical trapping of metal nanoparticles has focussed on a wavelength regime far from the particle’s resonance in the infrared. We experiment with laser wavelengths close to the plasmon resonance and expand the knowledge of metal nanoparticle trapping available to date. Existing theoretical models are put to the test when we compare these with our real experimental situations.EThOS - Electronic Theses Online Servicesdw - Stiftung der Deutschen WirtschaftGBUnited Kingdo

Measuring nanoparticle flow with the image structure function

We present a technique to measure the velocity and flow profiles of a nanofluid in a microfluidic channel. Importantly, we extract the flow velocity from a series of standard brightfield images without employing particle tracking or laser-enhanced methods. Our analysis retrieves the flow information from the image structure function of sub-diffraction limited nanoparticles in suspension. We are able to spatially resolve the flow velocity and map out the parabolic flow profile across the width of a microfluidic channel