Actuellement, les recherches sur la fonctionnalisation des surfaces sont en pleine effervescence. Dans ce manuscrit, nous proposons une approche innovante pour mesurer l’efficacité de cette fonctionnalisation. Cette approche est basée sur l’utilisation d’un microscope à force atomique, opérant dans un mode dit de « modulation de fréquence ». Cet outil couplé aux pointes greffées d’un nanotube de carbone, que nous appellerons « sonde », permet d’obtenir des mesures qu’il serait impossible d’effectuer avec des pointes standards. En métrologie, afin d’assurer une bonne reproductibilité des mesures, nous avons besoin d’avoir des sondes ayant des caractéristiques les plus similaires possibles. Ceci a nécessité la mise en oeuvre d’une méthode pour optimiser la fabrication des sondes, ainsi qu’une définition de critères pour les classer dans différents grades de qualités. L’incertitude de répétabilité et de reproductibilité des mesures effectuées avec des sondes de grade « A » a été quantifiée. Ces mesures ont démontré que ces sondes sont compatibles en termes de robustesse et de sensibilité pour la caractérisation de surfaces fonctionnalisées, dont l’épaisseur est supérieure à la monocouche. Des mesures de cartographie effectuées sur de deux types de surfaces fonctionnalisées ont permis de dissocier la mesure de topographie de la réponse mécanique du nanotube en interaction avec la surface. / At present, the researches on the surface functionalization are in full effervescence. In this manuscript, we propose an innovative approach to measure the efficiency of this functionalization. This approach is based on the use of an atomic force microscope, operating in a mode called "frequency modulation". This tool coupled with the grafted tips with a carbon nanotube, which we will call "probe", allows to obtain measurements which would be impossible to make with standard tips. However, in metrology, in order to ensure good reproducibility of the measurements, we need to have probes with characteristics that are as similar as possible. This required the implementation of a method to optimize the manufacture of the probes, as well as a definition of criteria to classify them in different grades of qualities. The uncertainty of repeatability and reproducibility of the measures made with probes of rank "A" were quantified. These measurements have demonstrated that these probes are compatible in terms of robustness and sensitivity for the characterization of functionalized surfaces, whose thickness is superior to the monolayer. Mapping measurements carried out on two types of functionalized surfaces enable to dissociate the topography measurement from the mechanical response of the nanotube in interaction with the surface.

No description available.

Malgré l'enthousiasme croissant pour les nanotechnologies, les nanoparticules (NPs) peuvent interagir avec les systèmes biologiques et affecter leur comportement, et pourraient ainsi présenter un danger pour les écosystèmes et l’Homme. Il est donc essentiel de connaître leurs mécanismes d'interactions afin non seulement de prévenir leurs risques potentiels, mais également de bénéficier de leurs propriétés uniques, par exemple dans la conception des biocapteurs. Dans ce contexte, nous étudions la cytotoxicité des NPs de silice, de tailles et charges diverses, sur les propriétés des bactéries Escherichia coli et Bacillus subtilis, au moyen de la microscopie à force atomique et des tests de viabilité. Les NPs chargées négativement (NPs-) de diamètre inférieur à un diamètre critique φc, 50 - 80 nm, (i) mènent à l'isolation des bactéries E. coli, (ii) induisent une "sphérification" de la cellule initialement en bâtonnet, (iii) provoquent des lésions dans la membrane externe et une réorganisation de sa structure. Pour la bactérie B. subtilis, seule la dégradation de la structure du peptidoglycane a été observée. Cependant, pour les deux souches, une activité antibactérienne a été démontrée pour les NPs- en dessous de φc, qui peuvent conduire à la lyse cellulaire tandis que, au-dessus de φc, les NPs- n’ont aucun effet sur la population, la morphologie ou la structure bactérienne. En ce qui concerne les NPs chargées positivement, elles conduisent, quel que soit leur diamètre, à une forte agrégation des cellules, en raison des interactions électrostatiques, et tendent à favoriser la formation d'invaginations membranaires, ne menant pas nécessairement à la lyse cellulaire. Cette étude fondamentale a mené au développement d’un biocapteur électrochimique pour la détection de bactéries, application notable pour des problèmes biomédicaux, environnementaux et de défense. Les NPs, intégrées à ces outils, offrent un mode de détection rapide, très sensible et peu coûteux. Expérimentalement, une multicouche de polyélectrolytes a été utilisée pour immobiliser des NPs inoffensives (φ = 100 nm), auxquelles sont ensuite fixés des anticorps spécifiques, afin d'améliorer la détection finale de la bactérie E. coli. L’ensemble des étapes a été optimisé par le procédé du spin coating et étudié à l'aide de mesures de microbalance à quartz et de voltametrie cyclique. L’intégration de NPs au biocapteur a permis une détection linéaire et non saturée des bactéries E. coli dans une large gamme de concentration (jusqu’à 10^9 CFU/mL) pour une limite de détection de 10^6 CFU/mL. / Despite the growing enthusiasm for nanotechnologies, nanoparticles (NPs) might put environmental safety and human health at risk, as they can interact with biological systems and affect their behavior. It is therefore essential to know their mechanisms of interactions in order not only to prevent their potential risks but also to benefit from their unique properties, such as in biosensors design. In this context, we study the cytotoxicity of silica NPs, with diverse sizes and charges, on the properties of Escherichia coli and Bacillus subtilis bacteria, by means of atomic force microscopy and viability tests. Negatively charged NPs (NPs-) with a diameter φ lower than a critical diameter φc, 50 - 80 nm, (i) lead to the isolation of E. coli bacteria, (ii) induce a "spherification" of the cell initially rod shaped, and (iii) cause the formation of pore-like lesions in the outer membrane and a reorganization of its structure. For B. subtilis bacteria, only the degradation of the peptidoglycane’s structure was observed. Though, for both strains, an antibacterial activity was shown for NPs- below φc, which potentially lead to the cell lysis whereas, above φc, NPs- have no effect on population, morphology or bacterial structure. As positively charged NPs are concerned, whatever their diameter, they lead to a strong aggregation of the cells, due to electrostatic interactions, and tend to favor the formation of membrane invaginations, not necessarily involving cell lysis. This fundamental study has been used to develop an electrochemical biosensor for bacteria, which are of great importance for biomedical, environmental and defense issues. NPs involved in such tools offer a fast, high-sensitive and low-cost way of detection. A polyelectrolyte multilayer was used to immobilize harmless NPs (φ = 100 nm), which are, then, functionalized with specific antibodies, in order to enhance the final detection of E. coli bacteria. All steps were optimized by a spin coating process and studied through quartz microbalance and cyclic voltametry measurements. Integrating NPs in this biosensor resulted in a linear and unsaturated detection of E. coli bacteria in a wide range of concentration (until 10^9 CFU/mL) and a limit of detection of 10^6 CFU/mL.

COSTA, Erivelton Façanha da. Estudo das propriedades mecânicas de misturas asfálticas por microscopia de força atômica. 2011. 131 f. Tese (Doutorado em Física) - Programa de Pós-Graduação em Física, Departamento de Física, Centro de Ciências, Universidade Federal do Ceará, Fortaleza, 2011. / Submitted by Edvander Pires (edvanderpires@gmail.com) on 2015-05-05T21:11:07Z No. of bitstreams: 1 2011_tese_efcosta.pdf: 9690898 bytes, checksum: 515b97b02ebfcf8c3652b217cd15491b (MD5) / Approved for entry into archive by Edvander Pires(edvanderpires@gmail.com) on 2015-05-07T16:57:29Z (GMT) No. of bitstreams: 1 2011_tese_efcosta.pdf: 9690898 bytes, checksum: 515b97b02ebfcf8c3652b217cd15491b (MD5) / Made available in DSpace on 2015-05-07T16:57:29Z (GMT). No. of bitstreams: 1 2011_tese_efcosta.pdf: 9690898 bytes, checksum: 515b97b02ebfcf8c3652b217cd15491b (MD5) Previous issue date: 2011 / The rheological study of asphalt binders is of great importance for determining its performance in paving construction. Usually, rheological parameters are obtained by a Dynamic Shear Rheometer (DSR). The aim of this work is to study the rheological properties of bitumen using an Atomic Force Microscope (AFM). So, a computational tool caled FVLOAD was used for imaging processing. Five kinds of mathematical models were used in order to analise the force curves colected through AFM: the slope analysis, the Young´s model, the adesion model, the FIEL model (Force Integration to Equal Limits) and the work difference model. Three samples were studied: pure bitumen 50/70, bitumem 50/70 doped with 4% of EVA and bitumem 50/70 doped with 4,5% of SBS. Very thin lms of these materials were prepared on glass slides and lead to an AFM for imaging. The area studied on the sample surface was of 50 m x 50 m. There were colected 1024 force curves for each image. The indentations were carried out in four frequencies: 0,5 Hz, 5 Hz, 14 Hz e 28 Hz. The curves colected were analyzed with the FVLOAD program and once the elastic properties were calculated, they were compared to those obtained in the Dynamic Shear Rheometer. / O estudo reológico do Cimento Asfáltico de Petróleo (CAP) é de fundamental importância para a determinação de sua performance na fabricação de estradas. Usualmente os parâmetros reológicos deste tipo de material são obtidos em ensaios dinâmicos através de um reômetro de cisalhamento. O presente trabalho tem por objetivo estudar as propriedades reológicas do CAP através da técnica de espectroscopia de força utilizando um microscópio de força atômica. Para isso, foi utilizada uma ferramenta computacional desenvolvida para o processamento das imagens de microscopia de força chamada de FVLOAD. Cinco análises foram realizadas com os dados das curvas de força: análise de slope, análise do módulo elástico ou módulo de Young, análise de adesão do filme de CAP, análise FIEL (Force Integration to Equal Limits), Work Difference e Adesão. Três amostras foram utilizadas neste estudo: CAP puro 50/70, CAP com 4% de EVA e CAP com 4,5% de SBS. Filmes dos três tipo de CAP foram confeccionados em lamínulas de vidro e levados ao microscópio de força atômica para obtenção dos dados das curvas de força sobre uma área de 50 μm x 50 μm. Para cada imagem foram coletadas 1024 curvas de força. As indentações com a sonda AFM foram executadas em quatro frequências: 0,5 Hz, 5 Hz, 14 Hz e 28 Hz. Finalizadas as aquisições de dados, estes foram processados no programa FVLOAD. Extraído o módulo elástico das amostras em cada frequência, os dados foram comparados com aqueles obtidos em ensaios dinâmicos através do reômetro de cisalhamento dinâmico.

abstract: The atomic force microscope (AFM) is capable of directly probing the mechanics of samples with length scales from single molecules to tissues and force scales from pico to micronewtons. In particular, AFM is widely used as a tool to measure the elastic modulus of soft biological samples by collecting force-indentation relationships and fitting these to classic elastic contact models. However, the analysis of raw force-indentation data may be complicated by mechanical heterogeneity present in biological systems. An analytical model of an elastic indentation on a bonded two-layer sample was solved. This may be used to account for substrate effects and more generally address experimental design for samples with varying elasticity. This model was applied to two mechanobiology systems of interest. First, AFM was combined with confocal laser scanning fluorescence microscopy and finite element analysis to examine stiffness changes during the initial stages of invasion of MDA-MB-231 metastatic breast cells into bovine collagen I matrices. It was determined that the cells stiffen significantly as they invade, the amount of stiffening is correlated with the elastic modulus of the collagen gel, and inhibition of Rho-associated protein kinase reduces the elastic modulus of the invading cells. Second, the elastic modulus of cancer cell nuclei was investigated ex situ and in situ. It was observed that inhibition of histone deacetylation to facilitate chromatin decondenstation result in significantly more morphological and stiffness changes in cancerous cells compared to normal cells. The methods and results presented here offer novel strategies for approaching biological systems with AFM and demonstrate its applicability and necessity in studying cellular function in physiologically relevant environments. / Dissertation/Thesis / Doctoral Dissertation Physics 2015

abstract: Cell adhesion is an important aspect of many biological processes. The atomic force microscope (AFM) has made it possible to quantify the forces involved in cellular adhesion using a technique called single cell force spectroscopy (SCFS). AFM based SCFS offers versatile control over experimental conditions for probing directly the interaction between specific cell types and specific proteins, surfaces, or other cells. Transmembrane integrins are the primary proteins involved in cellular adhesion to the extra cellular matix (ECM). One of the chief integrins involved in the adhesion of leukocyte cells is αMβ2 (Mac-1). The experiments in this dissertation quantify the adhesion of Mac-1 expressing human embryonic kidney (HEK Mac-1), platelets, and neutrophils cells on substrates with different concentrations of fibrinogen and on fibrin gels and multi-layered fibrinogen coated fibrin gels. It was shown that multi-layered fibrinogen reduces the adhesion force of these cells considerably. A novel method was developed as part of this research combining total internal reflection microscopy (TIRFM) with SCFS allowing for optical microscopy of HEK Mac-1 cells interacting with bovine serum albumin (BSA) coated glass after interacting with multi-layered fibrinogen. HEK Mac-1 cells are able to remove fibrinogen molecules from the multi-layered fibrinogen matrix. An analysis methodology for quantifying the kinetic parameters of integrin-ligand interactions from SCFS experiments is proposed, and the kinetic parameters of the Mac-1 fibrinogen bond are quantified. Additional SCFS experiments quantify the adhesion of macrophages and HEK Mac-1 cells on functionalized glass surfaces and normal glass surfaces. Both cell types show highest adhesion on a novel functionalized glass surface that was prepared to induce macrophage fusion. These experiments demonstrate the versatility of AFM based SCFS, and how it can be applied to address many questions in cellular biology offering quantitative insights. / Dissertation/Thesis / Doctoral Dissertation Physics 2016

Le rayonnement synchrotron et la microscopie à sondes locales (SPM) sont deux des techniques les plus utilisées pour étudier les propriétés physiques et chimiques de nanostructures. Le couplage de ces deux techniques est prometteur pour les nanosciences en leur ouvrant de nouveaux horizons. D'un point de vue expérimental ce couplage est un défi exaltant et a déjà prouvé ses capacités par la combinaison de la Microscopie à Force Atomique (AFM) et de la diffraction de Rayons-X pendant le projet X-tip, qui, grâce au développement d'un microcope à force atomique embarqué sur une lugne de lumière synchrotron a permis l'étude du module de Young de microplots de germanium en procédant simulatanément à son indentation et à son analyse par diffraction. Cependant, cette configuration ne permet pas de manipuler en trois dimensions (3D). Le but ultime, pour notre nano-manipulateur est de manipuler en 3D avec un contrôle permanent des nano-forces exercées sur l'objet sous un faisceau d'analyse (rayon X, LASER). Le premier chapitre s'attarde donc sur les senseurs qui devront rendre compte des interactions à l'échelle nanométrique et permettre la saisie d'un objet individuel. Après un tour d'horizon de différentes techniques de micro/nanomanipulation disponibles à ce jour (micro-préhenseurs mécaniques basés sur la technologie MEMS, pinces optiques, préhenseurs basés sur la microscopie à force atomique conventionnelle) et devant les contraintes qu'implique le couplage d'un tel système avec les expériences synchrotron, le choix des oscillateurs à quartz (Diapason et LER) en tant que senseurs est expliqué. La microscopie à force atomique en générale et le fonctionnement particulier de ces oscillateurs sont décrits. Dans le second chapitre le développement instrumental de notre station de nanomanipulation est détaillé et notamment : Comment mettre en place ce type de résonateurs et la pointe associée pour réaliser à la fois l'imagerie AFM de l'échantillon et la préhension de l'objet? Comment contrôler le positionnement grossier et fin des trois éléments d'une nanomanipulation? Enfin le système haptique ERGOS et son couplage avec notre montage est décrit. Dans le dernier chapitre, deux types d'expériences sont présentés : le premier ne fait intervenir que notre montage piloté classiquement par ordinateur et montre ses capacités à réaliser la préhension d'objets micrométriques de manière contrôlée. Le second fait intervenir le couplage entre notre montage et le système haptique pour réaliser l'exploration rapide d'un échantillon ainsi que la localisation et la reconnaissance de forme d'objet sub-micronique. Ces expériences rendent compte des capacités de ce couplage à transmettre directement à un utilisateur les interactions à l'échelle nanométrique ainsi que la possibilité par l'intermédiaire de cette interface de réaliser des tâches complexes : manipulation sur une surface, reconnaissance de forme, et suivi de contour. / The synchrotron radiation and scanning probe microscopy (SPM) are the (two) most used techniques to study the physical and chimical properties of nanostructures. Coupling these two techniques is promising for the nanosciences by opening news horizons. From an experimental point of view, this coupling is an exciting challenge and has already proven its skills with the combination of Atomic Force Microscopy (AFM) and X-Ray diffraction during the X-tip project, which, thanks to the development of an atomic force microscope embended on a synchrotron beamline, has permitted to study Young's modulus of germanium microplots proceeding simultaneously with its indentation and its diffraction analysis. However, this configuration doesn't permit a three dimension (3D) manipulation. The ultimate goal, for our nano-manipulator, is to manipulate in 3D with a permanent control of nano-forces exerted on the object undcer a scanning beam (X-Ray, laser). The first chapter therefore focuses on the sensors which measure the interactions at a nanometer scale and permit the seizure of an individual object. After an overview of the differents techniques of micro/nano-manipulation available today ( mechanical micro-grippers based on MEMS technology, optic tweezers, grippers based on conventionnal atomic force microscopy), and in front of the constraints implied by the coupling of this kind of system with the synchrotron experiments, the choice of quartz oscillators (Tunning fork and LER) as sensors is explained. The atomic force microscopy in general and the particular behavior of these oscillators is described. In the second chapter, the instrumental development of our nano-manipulation station is detailed and especially : How to implement this type of resonators and the associated tip to achieve both AFM imaging of the sample and gripping of the object ? How to control the coarse and fine positionning of the three elements of a nano-manipulation ? Finally, the haptic system ERGOS et its coupling with our assembly is describe. In the last chapter, two types of experiments are presented : the first involves only our assembly piloted classically with a computer and show its skills in the achievement of gripping of micrometric objects in a controled way. The second involves the coupling between our assembly and the haptic system to achieve the fast exploration of a sample and also the location and shape recognition of sub-micronic objects. These experiments reflect the capacities of this coupling to directly transmit to an user the interactions at a nanometer scale and also the possibility using this interface to achieve complex tasks : manipulation on a surface, shape recognition and contour tracking.

Le travail présenté dans se manuscrit s'inscrit dans le domaine de la chimie et physico-chimie des polysaccharides. Une étude des propriétés physico-chimiques du xyloglucane en fonction de différentes conditions est d'abords réalisée, elle montre la difficulté d'obtenir des solutions stables à l'échelle moléculaire ainsi que la possibilité d'obtenir des nanoparticules à base de xyloglucanes. Le suivi de l'hydrolyse enzymatique du xyloglucane en solution par la diffusion de la lumière a mis en évidence l'agrégation des produits obtenus en solution. L'imagerie par la microscopie à force atomique a révélé l'importance de la surface dans le phénomène de dégradation. Enfin des dérivés de xyloglucane ont été obtenus par oxydation par le système TEMPO/NaOCl/NaBr, et des essais de préparation de conjugués xyloglucane-cytarabine ont été effectués. / The work presented in this manuscript is in the field of chemistry and physical chemistry of polysaccharides. A study of the physicochemical properties of xyloglucan under different conditions is carried around and showing the difficulty to obtaining stable solutions at the molecular level. The study also evidenced the possibility of obtaining nanoparticles based on xyloglucan. Monitoring of the enzymatic hydrolysis of xyloglucan in solution by light scattering indicated the aggregation of the degradation products. Imaging by atomic force microscopy revealed the importance of the surface in the degradation phenomenon. Finally xyloglucan derivatives were obtained by oxidation system TEMPO / NaOCl / NaBr, and test on the coupling of xyloglucan and cytarabine conjugates were made.

Atualmente, a avaliação das propriedades biomecânicas da córnea vem sendo considerada um parâmetro importante a ser determinado, uma vez que está relacionado a diversos procedimentos (diagnósticos e cirúrgicos) e oftalmopatias. Devido à complexa disposição de suas lamelas, o estroma corneal é considerado a camada que exerce maior influência sobre as propriedades elásticas da córnea. A busca por modelos experimentais no estudo das propriedades biomecânicas da córnea têm aumentado ultimamente, devido à dificuldade em se obter amostras de córnea humana para fins científicos. Logo, estudos comparativos entre a córnea humana e a suína vêm sendo desenvolvidos, e algumas similaridades foram identificadas entre estas duas espécies. O presente estudo tem como objetivo avaliar as propriedades biomecânicas de diferentes regiões da córnea suína por meio da microscopia da força atômica. Dezesseis bulbos oculares não escaldados, de oito animais da espécie suína, foram adquiridos em frigorífico local. Animais de diferentes raças, faixas de peso e idade foram utilizados neste estudo. Bulbos oculares frescos foram submetidos ao debridamento da camada epitelial da córnea, sendo posteriormente imersos em solução de dextran a 25%. Mensurações da paquimetria corneal em regiões central, superior, inferior, nasal e temporal foram realizadas em cada etapa do preparo das amostras. Após 24 horas submersas em solução de dextran, as córneas foram excisadas em fragmentos de aproximadamente 3 x 3 mm, conforme as regiões acima descritas. Tais fragmentos foram submetidos à avaliação pelo microscópio de força atômica, imersos em solução de dextran a 25%. Os valores do módulo de Young para cada fragmento foram obtidos com base no modelo de elasticidade de Hertz. O armazenamento de amostras de córnea em solução de dextran preveniu a hidratação excessiva destas, mantendo a paquimetria dentro dos valores considerados normais. Tanto a paquimetria quanto o módulo de elasticidade corneais não variaram dentre as regiões central, superior, inferior, nasal e temporal da córnea. A espessura e a elasticidade da córnea não diferiram frente à comparação de olhos contralaterais. Devido à facilidade de aquisição e aos resultados obtidos, a córnea suína pode ser empregada como modelo experimental na avaliação das propriedades biomecânicas corneais. / Currently, the assessment of corneal biomechanical properties has been considered an important parameter to be determined, since it is related to several procedures (diagnostic and surgical) and ocular diseases. Due to the complex arrangement of its lamellae, the corneal stroma is considered the layer that exert more influence on the elastic properties of the cornea. The demand for experimental models to study the biomechanical properties of the cornea has recently increased due to the difficulty in obtaining samples of human cornea for scientific purposes. Therefore, comparative studies between human and porcine cornea have been developed, and some similarities were identified between these two species. This study aims to evaluate the biomechanical properties of different regions of the porcine cornea using atomic force microscopy. Sixteen eyes, enucleated from eight animals, were purchased at a local slaughterhouse. Animals of different breeds, age and weight ranges were used in this study. Fresh eyeballs underwent debridement of the corneal epithelial layer, and subsequently immersed in 25% dextran solution. Measurements of corneal pachymetry in the central, superior, inferior, nasal, and temporal regions were performed at each stage of sample preparation. After 24 hours submerged in dextran solution, the corneas were excised into fragments of approximately 3 x 3 mm, according to the regions described above. These fragments were analysed by atomic force microscope immersed in 25% dextran solution. The values of Young modulus for each fragment were obtained from the elasticity model of Hertz. The storage of samples in dextran solution prevented their excessive hydration, keeping the pachymetry values within normal limits. Both corneal thickness and elastic modulus did not vary among the central, superior, inferior, nasal and temporal regions of the cornea. The thickness and elasticity of the cornea did not differ between right and left eyes. Due to the facility of acquisition and the results obtained, porcine cornea can be used as experimental model for assessment of corneal biomechanical properties.

Neste trabalho, foram comparadas as cinéticas de adsorção da enolase (2-fosfo-D-glicerato hidrolase) sobre substratos hidrofílicos (placas de silício não modificadas ou silanizadas com aminopropilsilano (APS)) com aquelas sobre substratos hidrofóbicos (placas de silício silanizadas com trimetilclorosilano (TMCS) ou recobertas com filme de PS (poliestireno)). O efeito da forma do substrato (plano x esférico) sobre a cinética de adsorção também foi estudado. Os substratos esféricos foram esferas de vidro não modificadas (caráter hidrofílico) e silanizadas com TMCS (caráter hidrofóbico). As curvas de cinética de adsorção em substratos planos obtidas por elipsometria in situ mostraram que o processo ocorre em três etapas: (1) difusão das moléculas para a interface sólido/líquido, (2) formação de uma monocamada adsorvida e (3) adsorção de outras moléculas sobre a monocamada e formação de multicamadas. As isotermas mostraram que a enolase não possui adesão preferencial em substratos hidrofílicos ou hidrofóbicos. A etapa (1) pode ser descrita pelo modelo de adsorção seqüencial aleatória, enquanto que as etapas (2) e (3) podem ser descritas pelo modelo de adsorção seqüencial cooperativa. Não foi observada influência da força iônica. Contudo, imagens da topografia das superfícies recobertas por enolase obtidas por microscopia de força atômica (in situ e no ar) mostraram que os agregados de moléculas adsorvidas podem se apresentar na forma esférica (força iônica alta) ou como fibrilas (força iônica baixa). Medidas de espalhamento de raios-X a baixo ângulo (SAXS) de uma solução de enolase (6 g/L NaCl 0,001 mol/L) mostraram que as moléculas possuem raio de giro de 29 Å. Portanto, a agregação é induzida pelas propriedades da superfície da monocamada e pela força iônica do meio. Medidas de ângulo de contato mostraram que substratos inicialmente hidrofóbicos se tornaram hidrofílicos após adsorção da enolase, enquanto que os hidrofílicos apresentaram tendência oposta. Medidas de espectroscopia de fotoelétrons de raios-X evidenciaram que a adsorção sobre silício é mais rápida do que sobre PS, corroborando com os resultados obtidos por elipsometria. A influência do pH na adsorção da enolase em silício e APS mostraram que a adsorção é máxima quando o valor de pH é próximo ao ponto isoelétrico da enzima. A cinética de adsorção da enolase em substratos esféricos hidrofílicos e hidrofóbicos, acompanhada por espectrofotometria UV-vis, mostrou que a quantidade de material adsorvido O nestas superfícies aumenta com o tempo de adsorção e concentração inicial de enolase em solução (efeito de cooperativismo), sendo que o valor final é muito mais elevado nos substratos esféricos do que nos planos. Pela metodologia utilizada não se pôde observar os três estágios característicos da cinética de adsorção obtida para substratos planos. A influência da força iônica somente foi observada na adsorção sobre os substratos esféricos em sistemas concentrados (cenolase > 0,5g/L). As moléculas de enolase permanecem ativas após adsorção nos substratos estudados. / This work aimed to compare the adsorption behavior of enolase (2-phospho-D- glycerate hydrolase) onto hydrophilic (silicon wafers and amino-terminated surfaces (APS)) and hydrophobic planar substrates (polystyrene (PS) film, TMCS). The effect of the substrate shape (planar x spherical) was also studied. The spherical substrates were glass beads, native and modified with TMCS, with hydrophilic and hydrophobic characters, respectively. The adsorption kinetics of enolase onto planar substrates (obtained by means of in situ ellipsometry) presented three distinct regions: (i) a diffusion controlled step, (ii) monolayer formation evidenced by an adsorption plateau and (iii) continuous, irreversible and asymptotic increase of the adsorbed amount with time. The early stages were described by the random sequential adsorption model (RSA), while the cooperative sequential adsorption (CSA) model described regions (ii) and (iii). The adsorption isotherms show that enolase has no preferential adhesion onto hydrophilic or hydrophobic substrates. No significant influence of ionic strength was observed on the adsorption behavior of enolase onto the planar substrates. On the other hand, atomic force microscopy (AFM) showed that at long adsorption time and low ionic strength enolase monolayer induced fibrillation of the incoming molecules. Such effect was not observed at high ionic strength. Increasing the adsorption time, aggregates appeared on the surface, suggesting multilayer formation. Small angle X-ray scattering (SAXS) measurements of enolase (c = 6.0g/L) in NaCl 0.00 1 mol/L solution yielded radius of gyration of 29 Å, confirming that aggregation was probably induced by the surface of enolase monolayer and screening effects. Contact angle measurements showed that PS surfaces became hydrophilic and silicon surfaces turned hydrophobic after the formation of the enolase biofilm. XPS measurements showed that enolase adsorption is faster onto hydrophilic silicon wafers than onto hydrophobic PS fim, corroborating with the ellipsometric measurements. The study of the influence of pH on the enolase adsorption on silicon and APS surfaces showed that was the highest pH was close to the enzyme isoelectric point. The adsorption kinetic curves of enolase onto spherical substrates (obtained by means of UV-vis spectrophotometry) showed that the adsorbed amount (F) increased as function of adsorption time and initial concentration of enolase. The highest F value was obtained on spherical substrates. The three adsorption steps, characteristic of enolase adsorption, could not be observed by means of the methodology used. The influence of ionic strength was observed only in concentrated enolase solutions (cenolase 0.5g/L). The immobilized enolase molecules kept their enzymatic activity, regardless the type of substrate.