Ce travail de thèse est principalement axé sur le développement d’une nouvelle méthode de manipulation de vortex d’Abrikosov individuels dans les supraconducteurs de type II. Cette méthode, rapide, efficace et précise, est basée sur l’optique en champ lointain et repose sur l’échauffement local du supraconducteur sous l’action d’un faisceau laser focalisé. Elle apporte une excellente alternative aux techniques existantes de manipulation de vortex, toutes basées sur l’utilisation de sondes locales, et donc intrinsèquement lentes et difficiles à mettre en oeuvre dans un environnement cryogénique. La combinaison de cette méthode à une technique d’imagerie magnéto-optique performante permet de déplacer des vortex individuels avec un taux de réussite de 100% et sur de grandes échelles limitées uniquement par le champ de l’objectif de microscope. Les vitesses de manipulation atteintes sont élevées, de l’ordre de 10 mm.s-1, mais encore limitées par l’instrumentation utilisée et loin des limites fondamentales offertes par cette méthode, estimées au km.s-1. La méthode de manipulation optique permet aussi de mesurer la distribution des forces de piégeage de chaque vortex d’un échantillon. En utilisant des puissances de chauffage laser permettant de dépasser localement la température critique, nous avons également pu étudier la pénétration des vortex à l’interface entre une zone normale et une zone supraconductrice.Durant ces travaux, nous avons aussi eu l’opportunité de mettre en évidence, par spectroscopie de molécules uniques, l’effet flexomagnétoélectrique dans un matériau multiferroïque, en employant un supraconducteur de type I comme générateur de champ magnétique inhomogène. Enfin, nous proposons à la fin de ce mémoire un concept de jonction Josephson créée tout optiquement, et dont les propriétés seraient contrôlables en temps réel par laser. / This thesis focuses on the development of a new manipulation technique to handle single Abrikosov vortices in type II superconductors. This fast, efficient and precise method is based on far field optics and rests on the local temperature elevation produced by a focused laser beam. It brings an excellent alternative to the existing techniques which are all based on local probes and thus heavy to implement in a cryogenic environment. The combination of this method with an efficient magneto-optical imaging system allows us to manipulate single vortices with a 100% rate of success on a large scale only limited by the field of view of the microscope objective. Manipulation speeds are high, of the order of 10 mm.s-1, but still limited by our setup and far from the fundamental limits offered by this technique, estimated to the km.s-1. This manipulation technique also allows to measure the pinning force of any single vortex in a superconducting sample. By using a high enough laser power which locally pushes the temperature above the critical temperature, we could also study the vortex penetration at the interface between normal and superconducting areas.In the course of this work, we also evidenced, with single molecule spectroscopy, the flexomagnetoelectric effect in a multiferoic material, by using a type I superconductor as a source of inhomogeneous magnetic field. Finally, we propose at the end of the manuscript the new concept of an optically created Josephson junctions, whose properties could be controlled in real time just with a laser beam.

Optical tweezers are a technique in which microscopic-sized particles, including living cells and bacteria, can be non-intrusively trapped with high accuracy solely using focused light. The technique has therefore become a powerful tool in the field of biophysics. Optical tweezers thereby provide outstanding manipulation possibilities of cells as well as semi-transparent materials, both non-invasively and non-destructively, in biological systems. In addition, optical tweezers can measure minute forces (< 10-12 N), probe molecular interactions and their energy landscapes, and apply both static and dynamic forces in biological systems in a controlled manner. The assessment of intermolecular forces with force measuring optical tweezers, and thereby the biomechanical structure of biological objects, has therefore considerably facilitated our understanding of interactions and structures of biological systems. Adhesive bacterial organelles, so called pili, mediate adhesion to host cells and are therefore crucial for the initial bacterial-cell contact. Thus, they serve as an important virulence factor. The investigation of pili, both their biogenesis and their expected in vivo properties, brings information that can be of importance for the design of new drugs to prevent bacterial infections, which is crucial in the era of increased bacterial resistance towards antibiotics. In this thesis, an experimental setup of a force measuring optical tweezers system and the results of a number of biomechanical investigations of adhesive bacterial organelles are presented. Force measuring optical tweezers have been used to characterize three different types of adhesive organelles under various conditions, P, type 1, and S pili, which all are expressed by uropathogenic Escherichia coli. A quantitative biophysical force-extension model, built upon the structure and force response, has been developed. It is found, that this model describes the biomechanical properties for all three pili in an excellent way. Various parameters in their energy landscape, e.g., bond lengths and transition barrier heights, are assessed and the difference in behavior is compared. The work has resulted in a method that in a swift way allows us to probe different types of pili with high force and high spatial resolution, which has provided an enhanced understanding of the biomechanical function of these pili. / Optisk pincett är en teknik i vilken mikrometerstora objekt, inkluderande levande celler och bakterier, beröringsfritt kan fångas och förflyttas med hög noggrannhet enbart med hjälp av ljus. Den optiska pincetten har därmed blivit ett kraftfullt verktyg inom biofysiken, som möjliggör enastående precisions-manipulering av celler och semi-transparenta objekt. Dessutom kan denna manipulation göras intracellulärt, dvs. utan att fysiskt öppna eller penetrera cellernas membran. Den optiska pincetten kan även mäta mycket små krafter och interaktioner (< 10-12 N) samt applicera både statiska och dynamiska krafter i biologiska system med utmärkt precision. Optisk pincett är därför en utmärkt teknik för mätning av intermolekylära krafter och för bestämning av biomekaniska strukturer och dess funktioner. Vissa typer av bakterier har specifika vidhäftningsorganeller som kallas för pili. Dessa förmedlar vidhäftningen till värdceller och är därför viktiga vid bakteriens första kontakt. En djupare förståelse av pilis uppbyggnad och biomekanik kan därmed ge information, som kan vara vital i framtagandet av nya mediciner som förhindrar bakteriella infektioner. Detta är av stor vikt i skenet av den ökande antibiotikaresistensen i vårt samhälle. I denna avhandling presenteras konstruktionen av en experimentell uppställning av kraftmätande optiskt pincett tillsammans med resultat från biomekaniska undersökningar av vidhäftande bakteriella organeller. Kraftmätande optisk pincett har använts för att karakterisera tre olika typer av pili, P, typ 1, och S pili, vilka kan uttryckas av uropatogena Escherichia coli. En kvantitativ biofysikalisk modell som beskriver deras förlängningsegenskaper under pålagd kraft har konstruerats. Modellen bygger på pilis strukturella uppbyggnad samt på dess respons som uppmäts med den kraftmätande optiska pincetten. Modellen beskriver de biomekaniska egenskaperna väl för alla tre pili. Dessutom kan ett antal specifika bindnings- och subenhetsparametrar bestämmas, t.ex. interaktionsenergier och bindningslängder. Skillnaden mellan dessa parametrar hos de tre pilis samt deras olika kraftrespons har jämförts. Detta arbete har dels resulterat i en förbättrad förståelse av pilis biomekaniska funktion och dels i en metod som, med hög noggrannhet, tillåter oss att bestämma ett antal biomekaniska egenskaper hos olika organeller på ett effektivt sätt.

Many scientists and engineers are turning to lab-on-a-chip systems for cheaper and high throughput analysis of chemical reactions and biomolecular interactions. In this work, we developed several lab-on-a-chip modules based on novel manipulations of individual microbeads inside microchannels. The first manipulation method employs arrays of soft ferromagnetic patterns fabricated inside a microfluidic channel and subjected to an external rotating magnetic field. We demonstrated that the system can be used to assemble individual beads (1-3µm) from a flow of suspended beads into a regular array on the chip, hence improving the integrated electrochemical detection of biomolecules bound to the bead surface. In addition, the microbeads can follow the external magnet rotating at very high speeds and simultaneously orbit around individual soft magnets on the chip. We employed this manipulation mode for efficient sample mixing in continuous microflow. Furthermore, we discovered a simple but effective way of transporting the microbeads on-chip in the rotating field. Selective transport of microbeads with different size was also realized, providing a platform for effective sample separation on a chip. The second manipulation method integrates magnetic and dielectrophoretic manipulations of the same microbeads. The device combines tapered conducting wires and fingered electrodes to generate desirable magnetic and electric fields, respectively. By externally programming the magnetic attraction and dielectrophoretic repulsion forces, out-of-plane oscillation of the microbeads across the channel height was realized. Furthermore, we demonstrated the tweezing of microbeads in liquid with high spatial resolutions by fine-tuning the net force from magnetic attraction and dielectrophoretic repulsion of the beads. The high-resolution control of the out-of-plane motion of the microbeads has led to the invention of massively parallel biomolecular tweezers.

After an intense development of optical tweezers as a biophysical tool during the last decades, quantitative experiments in living cells have not found in this technique its best ally, due, in part, to the lack of a reliable method to measure forces in complex environments. The attempts to overcome this problem either require complicated in situ calibrations, which make their use impossible in the study of dynamic processes, or they are inaccurate. Using a different approach, Steven Smith at Carlos Bustamante’s lab at the University of Berkeley developed a method based on the direct measurement of the momentum change of the trapping beam. However, its diffusion has been modest mainly because it requires a counter-propagating optical trapping system, which is difficult to implement and combine with other techniques. Although it has not been used for this purpose yet, it seems a more suitable method for in vivo experiments since the measurement depends only on some properties of the sensor apparatus but not on the experiment itself. On the other hand, the use of holographic optical tweezers in molecular biology experiments involving force and position measurements is still far from established. The existence of different effects associated to the use of spatial light modulators to create the optical traps has restricted their use. In this thesis, I present the work that I carried out in the Optical Trapping Lab – Grup de Biofotònica at the University of Barcelona related to these two subjects. During these years, I have focused on the implementation of the force detection method based on the conservation of the light momentum in single-beam optical traps, and on the analysis of several aspects of holographic tweezers oriented to their use in quantitative experiments.

This dissertation details our experiments on studying the Brownian motion of an optically trapped microsphere with ultrahigh resolution, and cooling of its motion towards the quantum ground state. We have trapped glass microspheres in water, air and vacuum with optical tweezers. We developed a detection system that can monitor the position of a trapped microsphere with Angstrom spatial resolution and microsecond temporal resolution. We studied the Brownian motion of a trapped microsphere in air over a wide range of pressures. We measured the instantaneous velocity of a Brownian particle. Our results provide direct verification of the Maxwell-Boltzmann velocity distribution and the energy equipartition theorem for a Brownian particle. For short time scales, the ballistic regime of Brownian motion is observed, in contrast to the usual diffusive regime. We are currently developing a new detection system to measure the instantaneous velocity of a Brownian particle in water. In vacuum, we have used active feedback to cool the three center-of-mass vibration modes of a trapped microsphere from room temperature to millikelvin temperatures with a minimum mode temperature of 1.5 mK, which corresponds to the reduction of the root mean square (rms) amplitude of the microsphere from 6.7 nm to 15 pm for that mode. The mean thermal occupation number of that mode is reduced from about 6.8$\times 10^8$ at 297 K to about 3400 at 1.5 mK. / text

The thesis details the design and characterization of an innovative optical tweezer system. Optical tweezers provide a relatively new technique for non-contact manipulation of micron-scale particles. They employ a laser beam to hold such particles at the laser’s focus. Optical tweezers are used for many scientific purposes, such as: measuring the mechanical properties of bio-molecules, cell and molecule sorting, stiction-less micro-manipulators, and fundamental research in physics. Typically, trap location has been controlled using steer-mirrors or spatial light modulators, operating without beam quality feedback. Here, an innovative trap control system has been developed, featuring a closed-loop adaptive optics system. The prototype system employs a deformable mirror and wavefront sensor to control trap position in three dimensions, while simultaneously removing beam aberrations. The performance of this system is investigated in terms of controllable range of trap motion, trap stiffness, and trap position stability.

A major focus of research in nanotechnology is the development of novel, high throughput techniques for fabrication of arbitrarily shaped surface nanostructures of sub 100 nm to atomic scale. A related pursuit is the development of simple and efficient means for parallel manipulation and redistribution of adsorbed atoms, molecules and nanoparticles on surfaces – adparticle manipulation. These techniques will be used for the manufacture of nanoscale surface supported functional devices in nanotechnologies such as quantum computing, molecular electronics and lab-on-achip, as well as for modifying surfaces to obtain novel optical, electronic, chemical, or mechanical properties. A favourable approach to formation of surface nanostructures is self-assembly. In self-assembly, nanostructures are grown by aggregation of individual adparticles that diffuse by thermally activated processes on the surface. The passive nature of this process means it is generally not suited to formation of arbitrarily shaped structures. The self-assembly of nanostructures at arbitrary positions has been demonstrated, though these have typically required a pre-patterning treatment of the surface using sophisticated techniques such as electron beam lithography. On the other hand, a parallel adparticle manipulation technique would be suited for directing the selfassembly process to occur at arbitrary positions, without the need for pre-patterning the surface. There is at present a lack of techniques for parallel manipulation and redistribution of adparticles to arbitrary positions on the surface. This is an issue that needs to be addressed since these techniques can play an important role in nanotechnology. In this thesis, we propose such a technique – thermal tweezers. In thermal tweezers, adparticles are redistributed by localised heating of the surface. This locally enhances surface diffusion of adparticles so that they rapidly diffuse away from the heated regions. Using this technique, the redistribution of adparticles to form a desired pattern is achieved by heating the surface at specific regions. In this project, we have focussed on the holographic implementation of this approach, where the surface is heated by holographic patterns of interfering pulsed laser beams. This implementation is suitable for the formation of arbitrarily shaped structures; the only condition is that the shape can be produced by holographic means. In the simplest case, the laser pulses are linearly polarised and intersect to form an interference pattern that is a modulation of intensity along a single direction. Strong optical absorption at the intensity maxima of the interference pattern results in approximately a sinusoidal variation of the surface temperature along one direction. The main aim of this research project is to investigate the feasibility of the holographic implementation of thermal tweezers as an adparticle manipulation technique. Firstly, we investigate theoretically the surface diffusion of adparticles in the presence of sinusoidal modulation of the surface temperature. Very strong redistribution of adparticles is predicted when there is strong interaction between the adparticle and the surface, and the amplitude of the temperature modulation is ~100 K. We have proposed a thin metallic film deposited on a glass substrate heated by interfering laser beams (optical wavelengths) as a means of generating very large amplitude of surface temperature modulation. Indeed, we predict theoretically by numerical solution of the thermal conduction equation that amplitude of the temperature modulation on the metallic film can be much greater than 100 K when heated by nanosecond pulses with an energy ~1 mJ. The formation of surface nanostructures of less than 100 nm in width is predicted at optical wavelengths in this implementation of thermal tweezers. Furthermore, we propose a simple extension to this technique where spatial phase shift of the temperature modulation effectively doubles or triples the resolution. At the same time, increased resolution is predicted by reducing the wavelength of the laser pulses. In addition, we present two distinctly different, computationally efficient numerical approaches for theoretical investigation of surface diffusion of interacting adparticles – the Monte Carlo Interaction Method (MCIM) and the random potential well method (RPWM). Using each of these approaches we have investigated thermal tweezers for redistribution of both strongly and weakly interacting adparticles. We have predicted that strong interactions between adparticles can increase the effectiveness of thermal tweezers, by demonstrating practically complete adparticle redistribution into the low temperature regions of the surface. This is promising from the point of view of thermal tweezers applied to directed self-assembly of nanostructures. Finally, we present a new and more efficient numerical approach to theoretical investigation of thermal tweezers of non-interacting adparticles. In this approach, the local diffusion coefficient is determined from solution of the Fokker-Planck equation. The diffusion equation is then solved numerically using the finite volume method (FVM) to directly obtain the probability density of adparticle position. We compare predictions of this approach to those of the Ermak algorithm solution of the Langevin equation, and relatively good agreement is shown at intermediate and high friction. In the low friction regime, we predict and investigate the phenomenon of ‘optimal’ friction and describe its occurrence due to very long jumps of adparticles as they diffuse from the hot regions of the surface. Future research directions, both theoretical and experimental are also discussed.

No description available.

Dans la première partie de cette thèse, nous étudions la cinétique de la complexation d'un double brin d'ADN par la protéine NCp7. Pour ce faire, nous étudions l'évolution des propriétés mécaniques de l'ADN au fur et à mesure de sa complexation, en étirant la complexe ADN/NCp7 à l'aide d'un montage de piégeage optique. Nous avons observé que la longueur de persistance du complexe diminue au fur et à mesure de la complexation. En utilisant un modèle statistique décrivant l'évolution de la flexibilité de l'ADN complexé par NCp7. Notre principal résultat est que la fraction//phi de paires de bases ayant réagi n'est pas une fonction linéaire du temps aux faibles //phi. Nous interprétons nos résultats en supposant que l'adsorption de NCp7 sur l'ADN est fortement coopérative. Dans deuxième chapitre, nous décrivons la dynamique de particules sondes dans une suspension vitreuse colloïdale de Laponite. La Laponite est une particule colloïdale discoïdale de 25nm de diamètre et de 0.92 nm d'épaisseur. Nous utilisons une expérience de microscopie en onde évanescente, et suivons le mouvement de particules fluorescentes de latex. Nous imageons ensuite ces particules. Nous montrons que, pour un mouvement possédant une seule échelle de temps caractéristique, elle est simplement une fonction linéaire du temps. Nous obtenons que, quelle que soit leur taille, le mouvement des particules sondes peut être décrit par une succession de deux modes dynamiques, où le mode le plus rapide correspond à la diffusion des particules dans un fluide viscoélastique. / In the first part of this thesis, we study the kinetics of the complexation of a double-stranded DNA byNCp7 protein. To do this, we study the evolution of mechanical properties of DNA and its complexation by stretching the DNA/NCp7 complex with a optical trap. We observed that the persistence length of the complex decreases progressively during the complexation. Using astatistical model we describe the evolution of the flexibility of DNA complexed with NCp7. Our main result is that the fraction phi of base pairs that have reacted is not a linear function of time at low phi.We interpret our results assuming that the adsorption of NCp7 on DNA is highly cooperative. In the second chapter, we describe the dynamics of probe particles in a colloidal glassy suspension of Laponite. Laponite is a colloidal discoidal particle of 25 nm in diameter and 0.92 nm thick. We take advantage of evanescent wave microscopy, and follow the movement of fluorescent latex particles.Then we image these particles. We show that for a movement that has a single characteristic time scale, it is simply a linear function of time. We find that, what ever their size, the motion of probe particles can be described by a succession of two dynamic modes, where the fastest mode corresponds to the diffusion of particles in a viscoelastic fluid.

Made available in DSpace on 2015-03-26T13:35:18Z (GMT). No. of bitstreams: 1 texto completo.pdf: 5613341 bytes, checksum: b10dc863b3516fce568d5d4513b2ee67 (MD5) Previous issue date: 2012-02-17 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / In this work, by using the optical tweezers technique, it was possible to study the changes on the mechanical properties of DNA - cisplatin complexes, as a function of some parameters such as the drug diffusion time and its concentration in the sample. A model was proposed in order to explain the behavior of the persistent length as a function of drug concentration, using only the data obtained from single molecule stretching experiments. Such analysis allow us to show that cisplatin binds cooperatively to the DNA molecule. In addition, DNA molecule compactation by the action of the drug, was characterized from studying the kinetics of some mechanical properties such as the radius of gyration and the maximum average end - to - end distance. / Neste trabalho, utilizando a técnica de pinçamento óptico, foi possível estudar as mudanças nas propriedades mecânicas dos complexos DNA - cisplatina, em função de alguns parâmetros de interesse, tais como: o tempo de difusão do fármaco e a concentração do fármaco na amostra. Um modelo foi proposto para explicar o comportamento do comprimento de persistência em função da concentração do fármaco, utilizando-se apenas os dados obtidos a partir dos experimentos de estiramento. Tal análise nos permitiu mostrar que a cisplatina se liga cooperativamente à molécula de DNA. Além disso, a compactação da molécula de DNA pela ação da cisplatina foi caracterizada a partir do estudo da cinética de algumas propriedades mecânicas, tais como: o raio de giro e a distância máxima ponta - à - ponta dos complexos.