The study for surfaced-immobilized nucleic acid probes in nanometer region in response to hybridization and to discrimination ofdifferent target nuclei acids. The hairpin locked nucleic acid (LNA-HP) isselected to be the probe molecule, and target molecules include perfect complementary (PC) and single mismatch (1MM). The self-assembledLNA-HP molecular nanospot is successfully prepared by liquid phaseAFM (Atomic Force Microscope)-based nanolithography technique, then in situ hybridization is carried out by using different targets (PC/1MM).To obtain the information of structure change, we use AFM to analyze therelative heights in the process of hybridization. The experimental results point out that (1) the structure changes of surface probe molecules maycorrelate with the AFM signal when target sequence hybridizes to the probe, (2) miniaturization of the size of the nucleic acid probe may promote hybridization efficiency and enhance the discrimination between PC and 1MM. Studies on whether the different chemical impetus in solution can affect conformation of the human telomeric DNA of sequence is conducted. A human talomeric DNA composed of ( 5¡¦-TTAGGG-3¡¦:5¡¦-CCCTAA-3¡¦ ) repeats, with a 100-200 nt ( T2AG3 ) repetitive unit overhang at 3¡¦ ends is chosen. This extended single-stranded sequence is called G-rich DNA, which forms the special G-quadruplex structure in solution containing sodium ions or potassium ions. The single-stranded sequence composed of ( C3TA2 ) repetitive units called C-rich DNA displays the i-motif folded structure in the low pH environment. These biomimetic DNA¡¦s are thiol-modified to self-assemble on gold surfaces. Separate measurements with AFM (the molecular thickness and rootmean- square roughness of the self-assembly monolayer of DNA ) and CD( circular dichroism ) ( structure characterization ) confirm the conformational changes of G-rich and C-rich DNA¡¦s on gold surface are indeed dependent of the presence of cations and protons.

The folding mechanism of several β-structures (e.g., β-hairpins and β-sheets) was studied using newly developed enhanced sampling methods along with MD simulations in all implicit solvent environments. The influence of different implicit solvent models on the folding simulation of β-structure was also tested. Through the analysis of the free energy landscape as the function of several suitable reaction coordinates, we observed that the folding of β-hairpins is actually a two-state transition. In addition, the folding free energy landscapes for those related hairpins indicate the apparent sequence dependence, which demonstrates different folding mechanisms of similar β-structures of varied sequence. We also found that the stability of backbone hydrogen bonds is determined by the turn sequence and the composition of hydrophobic core cluster in β-structures. Neither of these findings was reported before. The processive movement of kinesin was also studied at the mesoscopic level. We developed a simple physical model to understand the asymmetric hand-over-hand mechanism of the kinesin walking on the microtubule. The hand-over-hand motion of the conventional kinesin is reproduced in our model and good agreement is achieved between calculated and experimental results. The experimentally observed limping of the truncated kinesin is also perfectly described by our model. The global conformational change of kinesin heads (e.g., the power stroke of neck-linkers which works as lever-arms during the kinesin walking, the transition between open and closed states of the switch region of the nucleotide binding domain in each head induced by the nucleotide binding and release) was studied for both dimeric and monomeric kinesins using a coarse-grained model, anisotropic network model (ANM). At the same time Langevin mode analysis was used to study the solvent influence on the motions of the kinesin head mimicked by ANM. Additionally, the correlation between the neck-linker and the nucleotide binding site was also studied for dimeric and monomeric kinesins. The former shows the apparent correlation between two subdomains whereas the latter does not, which may explain the experimental observation that only the dimeric kinesin is capable of walking processively on the microtubule.

<p>In summary there currently exist techniques to discover miRNA however both require many calculations to be performed during the identification limiting their use at a genomic level. Machine learning techniques are currently providing the best results by combining a number of calculated and statistically derived features to identify miRNA candidates, however almost all of these still include computationally intensive secondary-structure calculations. It is the aim of this project to produce a miRNA identification process that minimises and simplifies the number of computational elements required during the identification process.</p>

In this doctoral thesis we study novel analogues based on R06 aptamers and targeting TAR hairpins of the HIV virus by means of surface plasmon resonance biosensor, which allows for sensitive and real-time monitoring of molecular interactions. We investigate seven different modifications placed at nine different positions on the R06 aptamer in order to find out their applicability in the construction of efficient and stable anti-TAR oligonucleotides. We also determine which positions are suitable for substitutions with a modification and interpret the results in the context of the local nucleotide geometries and interactions in the TAR/anti-TAR complex. In this doctoral thesis we further develop a new fluidic system. This fluidic system eliminates sample dispersion and intermixing effects and thus enables accurate monitoring of molecular interactions on the surface of an SPR chip. We also characterize experimental conditions on the surface of an oligonucleotide chip and their relations towards bio-molecular assays. Specifically, we study the shielding effect of monovalent and divalent cations, which are crucial for the interaction of negatively charged oligonucleotides.

Ce travail s’inscrit dans le cadre de la recherche relative au développement de biosenseurs à ADN électrochimiques. Des aspects fondamentaux, ainsi que des aspects d’application de la détection d’hybridation d’ADN sont envisagés.<p>Dans un premier temps, le comportement interfacial et le processus d’hybridation d’oligonucléotides d’ADN linéaires et ADN hairpin (structure en épingle à cheveux) nonmarqués sont étudiés en formant des monocouches auto-assemblées mixtes de monobrins d’ADN (ssADN) thiolés et d’un hydroxyalcanethiol (4-mercaptobutan-1-ol) par coadsorption spontanée sur des électrodes d’or polycristallin. L’immobilisation de monocouches mixtes ssADN/MCB est caractérisée par voie électrochimique et par spectroscopie des photoélectrons X. Des mesures de chronocoulométrie, en présence de [Ru(NH3)6]3+ (RuHex), permettent de déterminer la quantité d’ADN dans la monocouche mixte formée. Les résultats montrent que l’excès superficiel d’ADN linéaire est plus important que l’excès superficiel d’ADN hairpin sous des conditions de formation identiques.<p>La réaction de reconnaissance moléculaire d’hybridation est détectée par des mesures d’impédance en présence de [Fe(CN)6]3-/4-. L’hybridation se traduit dans le cas de l’ADN linéaire par une augmentation de la résistance au transfert d’électron Rct tandis que dans le cas de l’ADN hairpin, Rct diminue. Ces différences sont dues au plus faible recouvrement et au changement de conformation des molécules d’ADN hairpin lors de l’hybridation. Des mesures de réflectivité de neutrons nous ont permis de mettre en évidence l’augmentation de l’épaisseur du film d’ADN hairpin et de confirmer le changement conformationel ces sondes lors de la reconnaissance moléculaire.<p>Dans la seconde partie, nous présentons une nouvelle méthode électrochimique de détection d’hybridation, basée sur les interactions électrostatiques entre le complexe cationique RuHex et les groupements phosphates de l’ADN. Afin d’améliorer la détection des molécules de PNA (peptide nucleic acid) ont été immobilisées comme sondes de reconnaissance moléculaire. Après hybridation des sondes PNA avec le brin complémentaire, RuHex s’adsorbe sur l’ADN hybridé et un signal de réduction de ces complexes redox, enregistré par voltampérométrie alternative, constitue une signature claire de l’hybridation d’ADN à l’interface modifiée. Les interactions RuHex/PNA-ADN ont été étudiées. La constante d’adsorption de RuHex sur l’électrode modifiée PNA/MCB après hybridation est évaluée à 2,9 (±0,3) 105 M-1 en milieu Tris-HCl 0,01M, selon une isotherme de Langmuir.<p>Les performances analytiques de la méthode de détection (sensibilité, sélectivité et reproductibilité) ont été évaluées et optimisées pour la détection des séquences d’ADN du gène de l’ARNr 23S d’Helicobacter pylori. La méthode de détection électrochimique présentée est assez sélective pour permettre de discriminer les mutations ponctuelles A2143G et A2144C de la séquence de type sauvage. La diminution significative des signaux d’admittance enregistrés en présence des séquences mutées est attribuée à la capacité accrue de discrimination de mutations ponctuelles des molécules PNA.<p>La réponse de détection est linéaire en fonction du logarithme de la concentration de la cible d’ADN sur plus de quatre ordres de grandeur (10-6 M à 10-10 M). La limite de détection de l’oligonucléotide d’ADN complémentaire de 80 pM est très bonne. La méthode a été appliquée avec succès à la détection de fragments PCR complémentaires de 100 et 400 paires de bases, amplifiés à partir de souches SS1 d’H.pylori. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

Magister Scientiae - MSc / In summary there currently exist techniques to discover miRNA however both require many calculations to be performed during the identification limiting their use at a genomic level. Machine learning techniques are currently providing the best results by combining a number of calculated and statistically derived features to identify miRNA candidates, however almost all of these still include computationally intensive secondary-structure calculations. It is the aim of this project to produce a miRNA identification process that minimises and simplifies the number of computational elements required during the identification process. / South Africa

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No description available.

OCL1 (Outer Cell Layer 1) est le membre fondateur, chez le maïs, de la famille multigénique regroupant les facteurs de transcription HD-ZIP IV. La plupart de ces gènes s’exprime préférentiellement dans l’épiderme, et chez Arabidopsis l’étude de mutants a montré que certains HD-ZIP IV étaient essentiels pour la différenciation de cette couche cellulaire. Lors de ma thèse je me suis intéressée à la régulation du gène OCL1 par un petit ARN non codant. En effet, la conservation au sein des 3’UTR de plusieurs gènes HD-ZIP IV d’un motif de 21 nucléotides (nt) suggérait l’existence d’un tel mécanisme. J’ai mis en évidence que ce motif de 21 nt était conservé des Bryophytes aux Angiospermes et qu’il était toujours couplé à un second motif conservé d’une taille de 19 nt avec lequel il peut s’apparier pour former une structure secondaire de type tige-boucle. J’ai démontré l’existence d’un petit ARN ayant une séquence (quasi) complémentaire au site de 21 nt. La biogenèse de ce petit ARN de 24 nt que nous avons nommé small1, dépend de RDR2/ MOP1, DCL3 et Pol IV/ RMR6, composants normalement requis pour le mécanisme de RdDM. A l’aide d’un système GFP sensor, j’ai cependant mis en évidence que small1 régulait l’expression de son gène cible par inhibition de la traduction et non par RdDM. Ces expériences ont par ailleurs démontré qu’OCL1 n’est pas régulé uniquement par small1, mais également via un second mécanisme dans lequel pourrait intervenir la structure secondaire de type tige-boucle. Enfin, j’ai montré que small1 possède une extrémité 5’modifiée, expliquant ainsi son absence des banques de données et définissant aussi une nouvelle classe de petits ARN chez les plantes. / Small non-coding RNAs are versatile riboregulators that control gene expression at the transcriptional or post-transcriptional level, governing many facets of plant development and stress responses. We previously suggested the possible regulation of OCL1 (Outer Cell Layer1) by a small RNA based on the intriguing presence of two conserved motives of 19 and 21nt in its 3’UTR. ZmOCL1 is a founding member of the HD-ZIP IV gene family encoding plant specific transcription factors mainly involved in epidermis differentiation and specialization. Here we present evidence for the existence of a 24 nt small RNA complementary to ZmOCL1 3’UTR which accumulates preferentially in maize reproductive organs but also in Arabidopsis flowers and inflorescences. The biogenesis of this 24 nt small RNA (that we named small1) depends on MOP1/RDR2 and RMR6/POLIV and DCL3, components normally required for RNA-dependent DNA-methylation. Unexpectedly GFP-sensor experiments showed that small1 may regulate its target at the post-transcriptional level, mainly through translational inhibition. These experiments further highlighted the importance of additional 3’UTR sequences required for efficient target repression, possibly implicating a secondary stem-loop structure. Finally, we showed that small1 is modified at its 5’ end, which not only explains its absence from the current databases but also defines a novel class of plant small RNAs.

<p>A specific class of small-scale plasmas (column diameters in a sub-mm to mm range) at rarefied pressures (under 10 Torr) enclosed in glass tubes hold significant interest currently in the scope  of  tunable  plasma  devices.  Specifically,  applications  of  these  plasmas  include  plasma antennas and plasma photonic crystals. Reliable diagnostics are necessary for the development and implementation of these technologies as conventional tools are inadequate in such small-scale plasmas.</p> <p>Coherent microwave scattering in the Thomson regime (TMS) was recently demonstrated for diagnostics of electron number density in miniature free-standing laser-induced plasmas in air under  10  Torr  with  plasma  column  diameters  <  0.5  mm.  However,  measurements  by  TMS diagnostics have never been applied for small-scale plasma objects enclosed within glass tubes. Additionally, TMS measurements were never independently confirmed with a previously verified experimental technique. This work aims to validate results of TMS measurements for small-scale plasma  objects  enclosed  within  glass  tubes  using  the  previously  established  and  well-known hairpin resonator probe. A DC discharge plasma column of fairly large diameter (about 1.5 cm) is used in the experiments to ensure reliable non-intrusive measurements by the hairpin resonator probe.</p> <p>The experiments were conducted in a DC discharge tube with a diameter of 1.5 cm and a length of 7 cm. TMS diagnostics yielded electron number densities of about 5.9×10¹⁰cm^-3, 2.8 ×10¹⁰cm^-3and  1.8 ×10¹⁰cm^-3at  pressures  of  0.2,  0.5  and  2.5  Torr,  respectively.  The corresponding  densities  measured  with  the  hairpin  resonator  probe  were  4.8×10¹⁰cm^-3,  3.8 ×10¹⁰cm^-3 and 2.6 ×10¹⁰cm^-3. Discrepancies between the two techniques were within 30% and can be attributed mainly to inaccuracies in the sheath thickness estimation required the hairpin resonator probe results.</p>