Die Aufgabe des Proteins Arrestin ist die Beendigung der Signalweitergabe über den GPCR Signalweg. In Stäbchenzellen bindet Arrestin an Licht-aktiviertes phosphoriliertes Rhodopsin um die Signalweitergabe zu unterdrücken. Die Bindung von Arrestin an Rhodopsin erfolgt in zwei Schritten. Zunächst wechselwirkt Arrestin mit dem phosphorilierten C-Terminus von Rhodopsin und bildet einen prä-Komplex, dies induziert Konformationsänderungen im Arrestin wodurch die Bildung eines High-affinity Komplex unter Kopplung an den helikalen Kern des aktivierten Rezeptors erfolgen kann. Biochemische Untersuchungen und Kristallstrukturen haben einen Einblick in die Konformation des Komplexes aus Arrestin und Rhodopsin ermöglicht. In dieser Arbeit werden site-directed Fluorezenz Experimente angewandt um die strukturellen Änderungen zu untersuchen, die bei der Bindung von Arrestin an Rhodopsin ablaufen und der nterschiedlichen Bindungsmodi innerhalb der Wechselwirkung zwischen Arrestin und Rhodopsin. Insbesondere wird hier eine, bisher nicht beschriebene, Assoziation von Arrestin an die Membran untersucht. Des Weiteren wurden Erkenntnisse über die Struktur des prä-Komplexes gewonnen. Die Konformation vom Arrestin im prä-Komplex scheint die Konformation im Basalzustand nachzubilden unter Beteiligung zweier Kontaktstellen: Interaktion mit dem phosphorilierten C-Terminus des Rezeptors und Assoziation mit der Membran. Beim Übergang in den High-affinity Komplex durchläuft Arrestin eine Konformationsänderung in eine aktivere Konformation: der C-Terminus wird verdrängt, es erfolgt eine Neuausrichtung der zentralen flexiblen Schleifen und die Orientierung des Membranankers ändert sich. Die Aufgabe des prä-Komplexes ist somit Arrestin und den Rezeptor zusammen zu bringen sowie die korrekte Orientierung sicherzustellen um einen schnellen Übergang in den High-affinity Komplex zu ermöglichen. / The protein arrestin is responsible for termination of GPCR signalling. In the rod cell, arrestin binds light-activated phosphorylated rhodopsin in order to block further signal transduction. The binding of arrestin to rhodopsin is a two-step process. Arrestin first interacts with the phosphorylated receptor C-terminus in a pre-complex, which induces conformational changes in arrestin that allow coupling to the helical core of the active receptor in a high-affinity complex. Biochemical studies and crystal structures have provided insights into the conformation of the arrestin-rhodopsin complex. This dissertation describes site-directed fluorescence experiments, which were carried out to further investigate the conformational changes occurring upon arrestin binding to rhodopsin and the nature of different binding modes of the arrestin-rhodopsin interaction. In particular this involved characterization of a previously unidentified association of arrestin with the membrane, as well as further elucidation of the structure of the pre-complex. The conformation of arrestin in the pre-complex is indicated to resemble that of the basal state of arrestin, and involves two sites of contact: interaction with the phosphorylated receptor C-terminus, and association with the membrane. Upon transition to the high-affinity complex, arrestin undergoes a conformational change to a more active conformation: the auto-inhibitory C-tail is displaced, there is movement within the central flexible loops, and the orientation of the membrane anchor changes. The pre-complex therefore most likely functions to bring arrestin and the receptor into close contact, and in the correct orientation, to allow for fast transition to the high-affinity complex.

<p>In this thesis some multivariate spectroscopic methods for the analysis of solutions are proposed. Spectroscopy and multivariate data analysis form a powerful combination for obtaining both quantitative and qualitative information and it is shown how spectroscopic techniques in combination with chemometric data evaluation can be used to obtain rapid, simple and efficient analytical methods. These spectroscopic methods consisting of spectroscopic analysis, a high level of automation and chemometric data evaluation can lead to analytical methods with a high analytical capacity, and for these methods, the term high-capacity analysis (HCA) is suggested. It is further shown how chemometric evaluation of the multivariate data in chromatographic analyses decreases the need for baseline separation. </p><p>The thesis is based on six papers and the chemometric tools used are experimental design, principal component analysis (PCA), soft independent modelling of class analogy (SIMCA), partial least squares regression (PLS) and parallel factor analysis (PARAFAC). The analytical techniques utilised are scanning ultraviolet-visible (UV-Vis) spectroscopy, diode array detection (DAD) used in non-column chromatographic diode array UV spectroscopy, high-performance liquid chromatography with diode array detection (HPLC-DAD) and fluorescence spectroscopy. The methods proposed are exemplified in the analysis of pharmaceutical solutions and serum proteins.</p><p>In Paper I a method is proposed for the determination of the content and identity of the active compound in pharmaceutical solutions by means of UV-Vis spectroscopy, orthogonal signal correction and multivariate calibration with PLS and SIMCA classification. Paper II proposes a new method for the rapid determination of pharmaceutical solutions by the use of non-column chromatographic diode array UV spectroscopy, i.e. a conventional HPLC-DAD system without any chromatographic column connected. In Paper III an investigation is made of the ability of a control sample, of known content and identity to diagnose and correct errors in multivariate predictions something that together with use of multivariate residuals can make it possible to use the same calibration model over time. In Paper IV a method is proposed for simultaneous determination of serum proteins with fluorescence spectroscopy and multivariate calibration. Paper V proposes a method for the determination of chromatographic peak purity by means of PCA of HPLC-DAD data. In Paper VI PARAFAC is applied for the decomposition of DAD data of some partially separated peaks into the pure chromatographic, spectral and concentration profiles. </p>

No description available.

Cette thèse porte sur l’étude de la relation entre la structure et la fonction chez les cotransporteurs Na+/glucose (SGLTs). Les SGLTs sont des protéines membranaires qui se servent du gradient électrochimique transmembranaire du Na+ afin d’accumuler leurs substrats dans la cellule. Une mise en contexte présentera d’abord un bref résumé des connaissances actuelles dans le domaine, suivi par un survol des différentes techniques expérimentales utilisées dans le cadre de mes travaux. Ces travaux peuvent être divisés en trois projets. Un premier projet a porté sur les bases structurelles de la perméation de l’eau au travers des SGLTs. En utilisant à la fois des techniques de modélisation moléculaire, mais aussi la volumétrie en voltage imposé, nous avons identifié les bases structurelles de cette perméation. Ainsi, nous avons pu identifier in silico la présence d’une voie de perméation passive à l’eau traversant le cotransporteur, pour ensuite corroborer ces résultats à l’aide de mesures faites sur le cotransporteur Na/glucose humain (hSGLT1) exprimé dans les ovocytes. Un second projet a permis d’élucider certaines caractéristiques structurelles de hSGLT1 de par l’utilisation de la dipicrylamine (DPA), un accepteur de fluorescence dont la répartition dans la membrane lipidique dépend du potentiel membranaire. L’utilisation de la DPA, conjuguée aux techniques de fluorescence en voltage imposé et de FRET (fluorescence resonance energy transfer), a permis de démontrer la position extracellulaire d’une partie de la boucle 12-13 et le fait que hSGLT1 forme des dimères dont les sous-unités sont unies par un pont disulfure. Un dernier projet a eu pour but de caractériser les courants stationnaires et pré-stationaires d’un membre de la famille des SGLTs, soit le cotransporteur Na+/myo-inositol humain hSMIT2 afin de proposer un modèle cinétique qui décrit son fonctionnement. Nous avons démontré que la phlorizine inhibe mal les courants préstationnaires suite à une dépolarisation, et la présence de courants de fuite qui varient en fonction du temps, du potentiel membranaire et des substrats. Un algorithme de recuit simulé a été mis au point afin de permettre la détermination objective de la connectivité et des différents paramètres associés à la modélisation cinétique. / This thesis is about the structure/function relationship in Na+/glucose cotransporters (SGLTs). SGLTs are membrane proteins which use the Na+ transmembrane electrochemical gradient to accumulate their substrates within the cell. As an introduction, a short review of the current state of the field will be followed by a presentation of the different technics used in this work. This work can be divided in three main projects. In the first project, we investigated the structural basis of water permeation through SGLTs. By using molecular modeling technics, we have identified, in silico, a passive permeation pathway used by water to go through the cotransporter across the membrane. Using voltage-clamp volumetric measurement, we were able to corroborate these findings for hSGLT1 expressed in oocytes. A second project allowed elucidation of some of hSGLT1 structural characteristics through the use of dipicrylamine (DPA), a fluorescence acceptor whose repartition in the lipid membrane is voltage-dependant. Use of DPA concomitantly with voltage-clamp fluorescence and FRET (fluorescence resonance energy transfer) has clearly demonstrated the extracellular localisation of part of the 12-13 loop which was previously assumed to be intracellular. In addition, we have shown that hSGLT1 forms a dimeric structure where the subunits are linked by a disulfide bridge. A last project aimed at characterizing the steady-state and pre-steadystate currents of a member of the SGLT family named hSMIT2 (human Na/myo-inositol transporter 2). We showed that phlorizin is a poor inhibitor of pre-steady state currents following depolarisation, and the presence of a time, membrane potential and substrate dependent leak current. A simulated annealing algorithm was developed in order to allow objective determination of both the connectivity and the parameters associated with the optimal kinetic model.

Em face ao bom desempenho da agricultura brasileira, cresce tamb&eacute;m a responsabilidade por uma produ&ccedil;&atilde;o sustent&aacute;vel. Particularmente, o sistema produtivo da cana-de-a&ccedil;&uacute;car vem se adaptando a uma produ&ccedil;&atilde;o sem queima, e busca formas alternativas de manejo dos res&iacute;duos da produ&ccedil;&atilde;o que sejam sustent&aacute;veis tanto economicamente, quanto ambientalmente. Neste trabalho apresentamos resultados dos tratamentos de solo agricultur&aacute;vel com res&iacute;duos de i) cinzas de baga&ccedil;o de cana aplicado em cobertura e ii) torta de filtro na entrelinha da cultura, em diferentes doses. Avaliamos o impacto desses tratamentos no conte&uacute;do de carbono e na mat&eacute;ria org&acirc;nica do solo. Para determinar se os tratamentos podem ser considerados sequestradores de carbono e ambientalmente sustent&aacute;veis nos detemos na preserva&ccedil;&atilde;o seletiva como mecanismo de reten&ccedil;&atilde;o da mat&eacute;ria org&acirc;nica do solo, a qual leva a acumula&ccedil;&atilde;o de componentes org&acirc;nicos qu&iacute;micos mais recalcitrantes. Utilizamos as t&eacute;cnicas espectrosc&oacute;picas de fluoresc&ecirc;ncia de luz UV-Vis&iacute;vel, espectroscopia de fluoresc&ecirc;ncia matriz excita&ccedil;&atilde;o-emiss&atilde;o para avaliar a fra&ccedil;&atilde;o de &aacute;cido h&uacute;mico do solo e o aumento da recalcitr&acirc;ncia qu&iacute;mica, a fluoresc&ecirc;ncia induzida por laser (FIL) para observar a mat&eacute;ria org&acirc;nica como um todo e a espectroscopia de emiss&atilde;o &oacute;tica com plasma induzido por laser (LIBS) utilizada como uma nova ferramenta para avaliar o conte&uacute;do de carbono do solo. No tratamento de solo com adi&ccedil;&atilde;o de cinza de baga&ccedil;o de cana tivemos potencial de estoque de carbono na dose 40 t/ha. Quanto a torta de filtro, o carbono total do solo aumenta menos significativamente que na cinza, mas n&atilde;o houve potencial de estoque de carbono. Na fra&ccedil;&atilde;o &aacute;cido h&uacute;mico n&atilde;o observamos modifica&ccedil;&atilde;o do grau de humifica&ccedil;&atilde;o do solo com os tratamentos, mesmo a torta sendo um produto rico em mat&eacute;ria org&acirc;nica, por&eacute;m houve um aumento de grupos carbon&iacute;licos, que est&atilde;o associados ao aumento das intera&ccedil;&otilde;es intermoleculares favorecendo por exemplo a complexa&ccedil;&atilde;o do &aacute;cido h&uacute;mico com metais. Nossos resultados de fluoresc&ecirc;ncia induzida por laser apontam que a cinza possivelmente ofereceu melhora nas condi&ccedil;&otilde;es de crescimento da cultura havendo aumento de grupos alif&aacute;ticos na MOS. Conclu&iacute;mos portanto, que n&atilde;o houve impacto negativo para o estoque de carbono no solo e qualidade da mat&eacute;ria sob tratamento de adi&ccedil;&atilde;o de cinza de baga&ccedil;o de cana e torta de filtro. / Given the good performance of Brazilian agriculture, grows the responsibility for sustainable production. Particularly, the sugarcane production system has been adapting to a production without burning, and seeks alternative forms of waste management in production that are both economically and environmentally sustainable. We present results of arable soil treatments with i) sugarcane bagasse ash applied in coverage soil and ii) filter cake applied between the lines of culture in different doses. We assess the impact of these treatments on the content and quality of soil organic matter and carbon sequestration capacity. To determine if treatments can be considered environmentally sustainable and carbon sequestration we embrace the selective preservation as a retention mechanism of soil organic matter, which leads to accumulation of chemical organic compounds recalcitrant. We use bidimensional fluorescence UV-Visible spectroscopy and fluorescence excitation-emission matrix to assess the fraction of soil humic acid, the laser-induced fluorescence spectroscopy (LIF) for observing the whole organic matter and laser breakdown induced spectroscopy (LIBS) used as a new tool to assess the soil carbon content. The soil treatment with sugarcane bagasse ash had increased carbon stock in dose 40 t / ha. In humic acid fraction did not observe any change in the degree of humification treatment with AML, but there was an increase of carbonyl groups, which are associated with increased intermolecular interactions and enhancing the complexation of metals with humic acid. Our results suggest a possible improvement in crop growth conditions with an increase of aliphatic groups in MOS. The filter cake is no carbon content recorded, also did not observe any impact on soil organic matter with the incorporation of filter cake although this is a product rich in organic matter. In this context, we conclude that there was no negative impact on the carbon stock and quality of soil organic matter under treatment addition of sugarcane bagasse ash and filter cake.

Submitted by Eunice Novais (enovais@uepg.br) on 2018-06-28T19:18:21Z No. of bitstreams: 2 license_rdf: 811 bytes, checksum: e39d27027a6cc9cb039ad269a5db8e34 (MD5) Talita Rosas Ferreira.pdf: 3918159 bytes, checksum: 3af8401f079b1540a49f10a3f6fd3b2d (MD5) / Made available in DSpace on 2018-06-28T19:18:21Z (GMT). No. of bitstreams: 2 license_rdf: 811 bytes, checksum: e39d27027a6cc9cb039ad269a5db8e34 (MD5) Talita Rosas Ferreira.pdf: 3918159 bytes, checksum: 3af8401f079b1540a49f10a3f6fd3b2d (MD5) Previous issue date: 2018-04-23 / No presente estudo, foram investigados os efeitos da calagem superficial sobre: os atributos químicos, as propriedades de interação com a radiação e a estrutura (sistema poroso) de um Cambissolo Háplico alumínico. A estrutura do solo foi analisada em escala micrométrica, considerando monólitos (8×8×8 cm) e pequenos agregados do solo (2-4 e 1-2 mm de diâmetro). O experimento consistia de cinco faixas, uma delas em área de pasto, considerada como referência (REF) e representando as condições do solo antes da implementação do sistema de plantio direto (SPD), e as demais, sob SPD, receberam as seguintes doses de calcário: 0 (C0), 10 (C10), 15 (C15) e 20 (C20) t ha-1 aplicadas na superfície do solo. A coleta das amostras se deu aos trinta meses após o procedimento de calagem, nas camadas 0-10 cm (A) e 10-20 cm (B). Os atributos químicos do solo foram caracterizados de acordo com procedimentos experimentais padrões e a composição de óxidos do solo, obtida por meio de análise de espectroscopia de fluorescência de raios X (FRX), foi usada para o cálculo do coeficiente de atenuação de massa do solo (μm), por meio do código computacional XCOM, para as energias de ≈ 60 keV (241Am) e ≈ 662 keV (137Cs). Os valores de μm foram utilizados para calcular as demais propriedades de interação da radiação com o solo e para simular as variações causadas na densidade (D) e porosidade total (Pt) do solo. Para a análise da estrutura do solo, foram utilizadas imagens 3D de microtomografia computadorizada de raios X (μTC), com resolução espacial de 60 μm (monólitos), e de μTC utilizando radiação síncrotron (μTC-RS), com resolução espacial de 1,64 μm (agregados). A visualização, processamento e análise das imagens foram realizadas com o software Avizo Fire. Foram determinadas as seguintes propriedades micromorfológicas e geométricas: porosidade baseada na imagem (P’), número de poros (NP), distribuições de P’ e NP em função de intervalos de volume, comprimento, alongamento, formato, conectividade e tortuosidade dos poros (monólitos); e: P’, distribuições de P’ e NP em função de intervalos de volume, conectividade, tortuosidade e dimensão fractal (agregados). Complementarmente, a composição elementar dos agregados do solo foi avaliada por meio de medidas de FRX. Na maioria dos casos, os efeitos da calagem concentraram-se na camada A, onde houve melhora nos atributos químicos e, portanto, no grau de acidez do solo, bem como houve aumento nas propriedades de interação da radiação em função das doses de calcário. O aumento nas propriedades de interação da radiação foi mais acentuado para a energia de ≈ 60 keV em relação a ≈ 662 keV e, no primeiro caso, as mudanças causadas em μm promoveram variação considerável na D e Pt do solo, demonstrando a relevância do estudo. A exemplo dos efeitos da calagem sobre o sistema poroso de monólitos do solo, na camada A, ressalta-se o aumento de P’ e do número de poros em que o poro principal foi separado, os quais foram identificados como sendo mais alongados e mais conectados devido à calagem. A calagem promoveu ainda alterações no arranjo dos poros separados, em ambas as camadas, com a formação de poros cilíndricos na direção horizontal, o que pode ser atribuído ao estímulo da atividade da fauna do solo. Para os agregados de solo, na camada A, a porcentagem de cálcio foi elevada a um valor mais alto em agregados de 1-2 mm em comparação com aqueles de 2-4 mm, em função das doses de calcário. A calagem afetou negativamente a estrutura de pequenos agregados do solo, diminuindo a P’ e aumentando a tortuosidade de poros para agregados de 1-2 mm. Além disso, a calagem reduziu a dimensão fractal em agregados de ambas as classes de tamanhos, em acordo com o fato de que, com a calagem, poros maiores foram substituídos por poros menores em agregados de 1-2 mm, conforme análises de natureza quantitativa e qualitativa. / In the present study, effects of surface liming on: chemical attributes, soil-radiation interaction properties and the structure (porous system) of a Dystrudept soil were investigated. The soil structure was analyzed in micrometric scale, considering monoliths (8×8×8 cm) and tiny aggregates (2-4 and 1-2 mm in diameter). The trial consisted of five stripes, one of them under pasture, considered here as reference (REF), representing the soil conditions before the no-till system (NTS) implementation, and the remaining, under NTS, received the following lime rates: 0 (C0), 10 (C10), 15 (C15) and 20 (C20) t ha-1 on the soil surface. Samples were collected thirty months after the liming procedure, at the 0-10 cm (A) and 10-20 cm (B) soil layers. The soil chemical attributes were characterized according to standard experimental procedures and the soil oxide composition, obtained by X-ray fluorescence spectroscopy (XRF), was used for the calculation of the soil mass attenuation coefficient (μm), by means of the computer code XCOM, for the energies of ≈ 60 keV (241Am) amd ≈ 662 keV (137Cs). The μm values were used to calculate the remaining soil-radiation interaction properties and to simulate variations caused on soil density (D) and total porosity (Pt). For the soil structure analysis, 3D images of X-ray computed microtomography (μCT), with spatial resolution of 60 μm (monoliths), and 3D images of synchrotron radiation based X-ray computed microtomography (SR-μCT), with spatial resolution of 1,64 μm (aggregates) were used. The image visualization, processing and analysis were performed in the Avizo Fire software. The following micromorphological and geometrical properties were determined: image-based porosity (P’), number of pores (NP), distributions of P’ and NP as function of volume intervals, length, elongation, shape, connectivity, and tortuosity of pores (monoliths); and: P’, distributions of P’ and NP as function of volume intervals, connectivity, tortuosity, and fractal dimension (aggregates). Additionally, the elemental composition of the soil aggregates was evaluated by XRF. In the majority of cases, liming effects were concentrated at layer A, where there was an improvement of soil chemical attributes and, therefore, of soil acidity level, as well as there was an increase in the soil-radiation interaction properties as function of lime rates. The increase in soil-radiation interaction properties was more accentuated for the energy of ≈ 60 keV in relation to ≈ 662 keV and, in the former case, the μm variation promoted considerable variation in D and Pt, demonstrating the relevance of the study. Highlighted instances of liming effects on the porous system of the soil monoliths, at layer A, were an increase in P’ and in the number of pores into which the main soil pore was separated, which were identified as being longer and more connected due to liming. Moreover, liming promoted changes in the arrangement of the separated pores, at both soil layers, with the formation of cylindrical pores in the horizontal orientation, which can be attributed to stimulation of the soil fauna activity. Regarding the soil aggregates, at layer A, calcium was raised to a higher percentage in aggregates of 1-2 mm when compared to those of 2-4 mm, as function of the lime rates. Liming affected negatively the structure of the soil tiny aggregates, decreasing P’ and increasing the tortuosity of pores for 1-2 mm aggregates. Besides, liming decreased the fractal dimension in aggregates from both size classes, in accord to the fact that, with liming, larger pores were replaced by smaller ones in 1-2 mm aggregates, as both quantitatively and qualitatively analyzed.

Le but principal de cette thèse était d'étudier les caractéristiques de la matière organique dissoute (MOD) dans le bassin versant de la Seine. Ce travail a été réalisé dans le cadre du programme de recherche PIREN-Seine. Les travaux présentés ici visaient plus particulièrement à identifier les sources de MOD et à suivre son évolution dans les zones d’étude. L’analyse des propriétés optiques (UV-Visible, fluorescence) de la MOD, couplée aux traitements PARAFAC et ACP, a permis de discriminer différentes sources de MOD et de mettre en évidence des variations spatio-temporelles de ses propriétés. L’axe Seine, en aval de Paris, a notamment été caractérisé par l'activité biologique la plus forte. La MOD du bassin de l’Oise a montré des caractéristiques plus "humiques", tandis que le bassin de la Marne a été caractérisé par un troisième type spécifique de MOD. Il a d’autre part été mis en évidence la présence de MODs spécifiques dans chaque zone pour les échantillons prélevés en périodes d’étiage, alors qu’une distribution homogène des composants a été obtenue pour l’ensemble des échantillons prélevés en période de crue.Le rôle environnemental des colloïdes naturels étant étroitement lié à leur taille, il a d’autre part été développé une technique analytique/séparative originale pour l’étude de ce matériel complexe, un fractionnement par couplage flux/force avec flux asymétrique (AF4). Le fractionnement par AF4 des échantillons a confirmé la variabilité spatio-temporelle en composition et en taille de la MOD d'un site de prélèvement à un autre et a permis de distinguer différentes sources de MOD colloïdale confirmant les résultats de l’étude de ses propriétés optiques. / The main goal of this thesis was to investigate the characteristics of dissolvedorganic matter (DOM) within the Seine River catchment in the Northern part of France. ThisPhD thesis was performed within the framework of the PIREN-Seine research program. Theapplication of UV/visible absorbance and EEM fluorescence spectroscopy combined toPARAFAC and PCA analyses allowed us to identify different sources of DOM andhighlighted spatial and temporal variations of DOM properties. The Seine River wascharacterized by the strongest biological activity. DOM from the Oise basin seemed to havemore "humic" characteristics, while the Marne basin was characterized by a third specifictype of DOM. For samples collected during low-water periods, the distributions of the 7components determined by PARAFAC treatment varied between the studied sub-basins,highlighting different organic materials in each zone. A homogeneous distribution of thecomponents was obtained for the samples collected in period of flood.Then, a semi-quantitative asymmetrical flow field-flow fractionation (AF4) methodology wasdeveloped to fractionate DOM. The following optimized parameters were determined: across-flow rate of 2 ml min-1 during the focus step with a focusing time of 2 min and anexponential gradient of cross-flow from 3.5 to 0.2 ml min-1 during the elution step. Thefluorescence properties of various size-based fractions of DOM were evaluated by applyingthe optimized AF4 methodology to fractionate 13 samples, selected from the three sub-basins.The fluorescence properties of these fractions were analysed, allowing us to discriminatebetween the terrestrial or autochthonous origin of DOM.

In this thesis some multivariate spectroscopic methods for the analysis of solutions are proposed. Spectroscopy and multivariate data analysis form a powerful combination for obtaining both quantitative and qualitative information and it is shown how spectroscopic techniques in combination with chemometric data evaluation can be used to obtain rapid, simple and efficient analytical methods. These spectroscopic methods consisting of spectroscopic analysis, a high level of automation and chemometric data evaluation can lead to analytical methods with a high analytical capacity, and for these methods, the term high-capacity analysis (HCA) is suggested. It is further shown how chemometric evaluation of the multivariate data in chromatographic analyses decreases the need for baseline separation. The thesis is based on six papers and the chemometric tools used are experimental design, principal component analysis (PCA), soft independent modelling of class analogy (SIMCA), partial least squares regression (PLS) and parallel factor analysis (PARAFAC). The analytical techniques utilised are scanning ultraviolet-visible (UV-Vis) spectroscopy, diode array detection (DAD) used in non-column chromatographic diode array UV spectroscopy, high-performance liquid chromatography with diode array detection (HPLC-DAD) and fluorescence spectroscopy. The methods proposed are exemplified in the analysis of pharmaceutical solutions and serum proteins. In Paper I a method is proposed for the determination of the content and identity of the active compound in pharmaceutical solutions by means of UV-Vis spectroscopy, orthogonal signal correction and multivariate calibration with PLS and SIMCA classification. Paper II proposes a new method for the rapid determination of pharmaceutical solutions by the use of non-column chromatographic diode array UV spectroscopy, i.e. a conventional HPLC-DAD system without any chromatographic column connected. In Paper III an investigation is made of the ability of a control sample, of known content and identity to diagnose and correct errors in multivariate predictions something that together with use of multivariate residuals can make it possible to use the same calibration model over time. In Paper IV a method is proposed for simultaneous determination of serum proteins with fluorescence spectroscopy and multivariate calibration. Paper V proposes a method for the determination of chromatographic peak purity by means of PCA of HPLC-DAD data. In Paper VI PARAFAC is applied for the decomposition of DAD data of some partially separated peaks into the pure chromatographic, spectral and concentration profiles.

Arthropod hemocyanin and phenoloxidase are members of a group of proteins called the Type-3 copper oxygen-binding proteins, both possessing a highly conserved oxygen-binding site containing two copper atoms each coordinated by three histidine residues (Decker and Tuczek, 2000). Despite similarities in their active site, these proteins have very different physiological functions. Phenoloxidase possesses both tyrosinase and o-diphenoloxidase activity, and is predominantly involved in reactions which protect insects from infection (Kopàcek et al., 1995). Hemocyanin is a large multi-subunit protein with a primary function as a respiratory protein, reversibly binding and transporting molecular O2 (Decker and Rimke, 1998; Decker and Tuczek, 2000). Recently, it has been demonstrated in vitro that arthropod hemocyanin possesses an inducible phenoloxidase activity when incubated with denaturants, detergents, phospholipids or proteolytic enzymes. This activity appears to be restricted to only a few subunit types, and it has been hypothesised that it may be accompanied by conformational change which opens the active site increasing access for larger phenolic substrates (Decker and Jaenicke, 2004; Decker et al., 2001; Decker and Tuczek, 2000). This possibly suggests a dual role of hemocyanin in arthropods. The presented thesis deals with two distinct aims. The first was to isolate and sequence a phenoloxidase gene from the insect Spodoptera littoralis (Egyptian Cottonleaf Worm). Despite efforts, progress was hindered by a number of experimental problems which are outlined within the relevant chapters. The second aim was to characterise the mode of SDS induced phenoloxidase activity in arthropod hemocyanin from the ancient chelicerates Limulus polyphemus (horseshoe crab) and Eurypelma californicum (tarantula) and the more modern chelicerate Pandinus imperator (scorpion), using a number of biophysical techniques. The results indicated that the SDS induced phenoloxidase activity is associated with localised tertiary and secondary conformational changes in hemocyanin, most likely in the vicinity of the dicopper centre, thus enhancing access for larger phenolic substrates. Experiments indicate that copper remains associated with the protein during these structural changes; however the nature of the association is unclear. SDS concentrations approximating the CMC appeared critical in causing the necessary structural changes required for a significant increase in the detectable phenoloxidase activity to be exhibited.

Cette thèse porte sur l’étude de la relation entre la structure et la fonction chez les cotransporteurs Na+/glucose (SGLTs). Les SGLTs sont des protéines membranaires qui se servent du gradient électrochimique transmembranaire du Na+ afin d’accumuler leurs substrats dans la cellule. Une mise en contexte présentera d’abord un bref résumé des connaissances actuelles dans le domaine, suivi par un survol des différentes techniques expérimentales utilisées dans le cadre de mes travaux. Ces travaux peuvent être divisés en trois projets. Un premier projet a porté sur les bases structurelles de la perméation de l’eau au travers des SGLTs. En utilisant à la fois des techniques de modélisation moléculaire, mais aussi la volumétrie en voltage imposé, nous avons identifié les bases structurelles de cette perméation. Ainsi, nous avons pu identifier in silico la présence d’une voie de perméation passive à l’eau traversant le cotransporteur, pour ensuite corroborer ces résultats à l’aide de mesures faites sur le cotransporteur Na/glucose humain (hSGLT1) exprimé dans les ovocytes. Un second projet a permis d’élucider certaines caractéristiques structurelles de hSGLT1 de par l’utilisation de la dipicrylamine (DPA), un accepteur de fluorescence dont la répartition dans la membrane lipidique dépend du potentiel membranaire. L’utilisation de la DPA, conjuguée aux techniques de fluorescence en voltage imposé et de FRET (fluorescence resonance energy transfer), a permis de démontrer la position extracellulaire d’une partie de la boucle 12-13 et le fait que hSGLT1 forme des dimères dont les sous-unités sont unies par un pont disulfure. Un dernier projet a eu pour but de caractériser les courants stationnaires et pré-stationaires d’un membre de la famille des SGLTs, soit le cotransporteur Na+/myo-inositol humain hSMIT2 afin de proposer un modèle cinétique qui décrit son fonctionnement. Nous avons démontré que la phlorizine inhibe mal les courants préstationnaires suite à une dépolarisation, et la présence de courants de fuite qui varient en fonction du temps, du potentiel membranaire et des substrats. Un algorithme de recuit simulé a été mis au point afin de permettre la détermination objective de la connectivité et des différents paramètres associés à la modélisation cinétique. / This thesis is about the structure/function relationship in Na+/glucose cotransporters (SGLTs). SGLTs are membrane proteins which use the Na+ transmembrane electrochemical gradient to accumulate their substrates within the cell. As an introduction, a short review of the current state of the field will be followed by a presentation of the different technics used in this work. This work can be divided in three main projects. In the first project, we investigated the structural basis of water permeation through SGLTs. By using molecular modeling technics, we have identified, in silico, a passive permeation pathway used by water to go through the cotransporter across the membrane. Using voltage-clamp volumetric measurement, we were able to corroborate these findings for hSGLT1 expressed in oocytes. A second project allowed elucidation of some of hSGLT1 structural characteristics through the use of dipicrylamine (DPA), a fluorescence acceptor whose repartition in the lipid membrane is voltage-dependant. Use of DPA concomitantly with voltage-clamp fluorescence and FRET (fluorescence resonance energy transfer) has clearly demonstrated the extracellular localisation of part of the 12-13 loop which was previously assumed to be intracellular. In addition, we have shown that hSGLT1 forms a dimeric structure where the subunits are linked by a disulfide bridge. A last project aimed at characterizing the steady-state and pre-steadystate currents of a member of the SGLT family named hSMIT2 (human Na/myo-inositol transporter 2). We showed that phlorizin is a poor inhibitor of pre-steady state currents following depolarisation, and the presence of a time, membrane potential and substrate dependent leak current. A simulated annealing algorithm was developed in order to allow objective determination of both the connectivity and the parameters associated with the optimal kinetic model.