• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 640
  • 102
  • 78
  • 72
  • 37
  • 10
  • 9
  • 9
  • 9
  • 7
  • 4
  • 2
  • 2
  • 2
  • 1
  • Tagged with
  • 1193
  • 522
  • 224
  • 191
  • 184
  • 158
  • 143
  • 137
  • 113
  • 112
  • 112
  • 105
  • 97
  • 97
  • 96
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
361

Biomolecular Analysis by Dual-Tag Microarrays and Single Molecule Amplification

Ericsson, Olle January 2008 (has links)
Padlock probes and proximity ligation are two powerful molecular tools for detection of nucleic acids and proteins, respectively. Both methods result in the formation of DNA reporter molecules upon recognition of specific target molecules. These reporter molecules can be designed to include tag sequences that can be analyzed by techniques for nucleic acid analysis. Herein, I present a dual-tag microarray (DTM) platform that is suitable for high-performance analyses of DNA reporter molecule libraries, generated by padlock and proximity probing reactions. The DTM platform was applied for analysis of mRNA transcripts using padlock probes, and of cytokines using proximity ligation. The platform drastically improved specificity of detection, and it allowed precise measurements of proteins and nucleic acids over wide dynamic ranges. The thesis also presents two techniques for multi-probe analyses of biomolecules: the triple-specific proximity ligation assay (3PLA) for protein analyses, and the spliceotyping assay for mRNA analyses. 3PLA allows highly specific measurements of as little as hundreds of target protein molecules by interrogating three target epitopes simultaneously. In spliceotyping the exon composition of individual transcripts are represented as a series of tag sequences in DNA reporter molecules, via a series of target-dependent ligation reactions. Next, the splicing patterns along individual transcripts can be revealed by amplified single molecule detection and step-wise decoding.
362

Kraftspektroskopie mittels optischer Pinzetten zur Untersuchung einzelner Rezeptor/Ligand-Komplexe

Wagner, Carolin 02 May 2013 (has links) (PDF)
Optische Pinzetten stellen neuartige Werkzeuge in der Biophysik dar, die sich durch eine außerordentliche Präzision auszeichnen. Im Rahmen der vorliegenden Arbeit werden verfeinerte Bildanalysetechniken vorgestellt und neu entwickelt, die es erlauben, die Position eines Mikropartikels mit einer zeitlichen Auflösung von 0,017 s und einer Genauigkeit von ±2nm in lateraler und in axialer Richtung zu bestimmen. Dies ermöglicht eine Kraftauflösung von bis zu ±50 fN. Damit sind die Voraussetzungen für die Untersuchung von Rezeptor/Ligand-Wechselwirkungen auf der Ebene einzelner Bindungsereignisse gegeben. In der vorliegenden Arbeit werden die Wechselwirkungen zwischen den phosphorylierungsspezifischen Antikörpern HPT-101, HPT-104 und HPT-110 und Tau-Peptiden mit verschiedenen Phosphorylierungsmustern sowie zwischen DNA und den Proteinen TmHU und oPrPC untersucht. Die Wechselwirkungen zwischen Tau-Peptiden und Antikörpern werden jeweils anhand ihrer Bindungshäufigkeit sowie der Verteilung der Abrisskräfte charakterisiert. Mit einem aus der Literatur bekannten, theoretischen Modell werden folgende Bindungsparameter bestimmt: Lebenszeit der unbelasteten Bindung, charakteristische Länge und freie Aktivierungsenergie der Dissoziation. Im Einklang mit Ergebnissen einer immunochemischen Messung werden spezifische Wechselwirkungen zwischen HPT-101 und dem biphosphorylierten Tau-Peptid sowie zwischen HPT-104 bzw. HPT-110 und den Peptiden, die eine Phosphorylierung an Thr231 bzw. Ser235 enthalten, beobachtet. Zusätzlich ermöglicht die Einzelmolekülmethode auch eine detaillierte Charakterisierung der unspezifischen Wechselwirkungen mit den Tau-Peptiden, welche das jeweilige spezifisch erkannte Phosphorylierungsmuster nicht beinhalten. Der zweite Teil der Arbeit befasst sich mit dem Einfluss der Proteine TmHU und oPrPC auf einen einzelnen, mit konstanter Kraft gehaltenen DNA-Strang. Der zeitliche Verlauf der TmHU-induzierten Kondensationsreaktion wird bei Kräften zwischen 2 pN und 40 pN sowie in Abhängigkeit von der Proteinkonzentration untersucht. Bei kleinen Kräften ist eine Verkürzung in zwei Phasen auf bis zu 30% der Konturlänge zu beobachten. Unter zusätzlicher Einbeziehung der Ergebnisse einer SMD-Simulation sowie einer rasterkraftmikroskopischen Untersuchung kann die erste Phase der Verkürzung einer primären Anbindung von TmHU zugeordnet werden. Die zweite Reaktionsphase entspricht hingegen vermutlich der Ausbildung einer Überstruktur. Die Wechselwirkung von oPrPC mit DNA wird zusätzlich mit einer kombinierten Anordnung aus Nanokapillare und optischer Pinzette untersucht. Dabei zeigt sich, dass ein Protein/DNA-Komplex ausgebildet wird, der eine negative Oberflächenladung aufweist und sich in seinem Volumen und seiner Ladung von reiner DNA unterscheidet. Allerdings hat oPrPC keinen Einfluss auf den Ende-zu-Ende-Abstand bzw. die Elastizität der DNA.
363

DNA Tools and Microfluidic Systems for Molecular Analysis

Jarvius, Jonas January 2006 (has links)
Improved methods are needed to interrogate the genome and the proteome. Methods with high selectivity, wide dynamic range, and excellent precision, capable of simultaneously analyzing many biomolecules are required to decipher cellular function. This thesis describes a molecular and microfluidic toolbox designed with those criteria in mind. It also presents a tool for graphical representation of nucleic acid sequences. Proximity ligation is a novel protein detection method that requires dual and proximate binding of two oligonucleotide-tagged affinity reagents to a protein or protein complex in order to elicit a signal. The responses from such recognition reactions are the formation of specific nucleic acid reporter molecules that are subsequently amplified and quantitatively detected. A scalable microfluidic platform suitable for fluorescence detection, cell culture, and actuation is also described. The platform uses rapid injection molding to produce microstructures in thermoplastic materials. By applying a thin layer of silica to the structures, a lid made of silicone rubber coated onto a thermoplastic support can be covalently bonded to generate enclosed channels. A method is presented for precise biomolecule counting, termed “amplified single-molecule detection”. The method preserves the discrete nature of biomolecules, converting specific molecular recognition events to fluorescence-labeled micrometer-sized objects that are enumerated in microfluidic channels. I also present a novel microarray-based detection method. To attain high selectivity and a wide dynamic range, the method is based on dual recognition with enzymatic discrimination and amplification. Upon target recognition in solution, DNA probes are subjected to thousand-fold amplification in solution, followed by selective detection on arrays and another hundred-fold amplification of reporter molecule created from the first amplification reaction. Lastly, I describe a novel graphical representation of nucleic acid sequences using TrueType fonts that can be of value for visual inspection of DNA sequences and for teaching purposes
364

Experimental Free Energy Landscape Reconstruction of DNA Unstacking Using Crooks Fluctuation Theorem

Frey, Eric 05 June 2013 (has links)
Nonequilibrium work theorems, such as the Jarzynski equality and the Crooks fluctuation theorem, allow one to use nonequilibrium measurements to determine equilibrium free energies. For example, it has been demonstrated that the Crooks fluctuation theorem can be used to determine RNA folding energies. We used single-molecule manipulation with an atomic force microscope to measure the work done on poly(dA) as it was stretched and relaxed. This single-stranded nucleic acid exhibits unique base-stacking transitions in its force-extension curve due to the strong interactions among A bases, as well as multiple pathways. Here we showed that free energy curves can be determined by using the Crooks fluctuation theorem. The nonequilibrium work theorem can be used to determine free energy curves even when there are multiple pathways.
365

Experimental Free Energy Landscape Reconstruction of DNA Unstacking Using Crooks Fluctuation Theorem

Frey, Eric 05 June 2013 (has links)
Nonequilibrium work theorems, such as the Jarzynski equality and the Crooks fluctuation theorem, allow one to use nonequilibrium measurements to determine equilibrium free energies. For example, it has been demonstrated that the Crooks fluctuation theorem can be used to determine RNA folding energies. We used single-molecule manipulation with an atomic force microscope to measure the work done on poly(dA) as it was stretched and relaxed. This single-stranded nucleic acid exhibits unique base-stacking transitions in its force-extension curve due to the strong interactions among A bases, as well as multiple pathways. Here we showed that free energy curves can be determined by using the Crooks fluctuation theorem. The nonequilibrium work theorem can be used to determine free energy curves even when there are multiple pathways.
366

Experimental Free Energy Landscape Reconstruction of DNA Unstacking Using Crooks Fluctuation Theorem

Frey, Eric 05 June 2013 (has links)
Nonequilibrium work theorems, such as the Jarzynski equality and the Crooks fluctuation theorem, allow one to use nonequilibrium measurements to determine equilibrium free energies. For example, it has been demonstrated that the Crooks fluctuation theorem can be used to determine RNA folding energies. We used single-molecule manipulation with an atomic force microscope to measure the work done on poly(dA) as it was stretched and relaxed. This single-stranded nucleic acid exhibits unique base-stacking transitions in its force-extension curve due to the strong interactions among A bases, as well as multiple pathways. Here we showed that free energy curves can be determined by using the Crooks fluctuation theorem. The nonequilibrium work theorem can be used to determine free energy curves even when there are multiple pathways.
367

Experimental Free Energy Landscape Reconstruction of DNA Unstacking Using Crooks Fluctuation Theorem

Frey, Eric 05 June 2013 (has links)
Nonequilibrium work theorems, such as the Jarzynski equality and the Crooks fluctuation theorem, allow one to use nonequilibrium measurements to determine equilibrium free energies. For example, it has been demonstrated that the Crooks fluctuation theorem can be used to determine RNA folding energies. We used single-molecule manipulation with an atomic force microscope to measure the work done on poly(dA) as it was stretched and relaxed. This single-stranded nucleic acid exhibits unique base-stacking transitions in its force-extension curve due to the strong interactions among A bases, as well as multiple pathways. Here we showed that free energy curves can be determined by using the Crooks fluctuation theorem. The nonequilibrium work theorem can be used to determine free energy curves even when there are multiple pathways.
368

KINETIC CHARACTERIZATION AND NEWLY DISCOVERED INHIBITORS FOR VARIOUS CONSTRUCTS OF HUMAN T-CELL LEUKEMIA VIRUS-I PROTEASE AND INHIBITION EFFECT OF DISCOVERED MOLECULES ON HTLV-1 INFECTED CELLS

DEMIR, AHU 21 October 2010 (has links)
Discovered in 1980, HTLV-1 (Human T-cell Leukemia Virus-1), was the first identified human retrovirus and is shown to be associated with a variety of diseases including: adult T-cell leukemia lymphoma (ATLL), tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM), chronic arthropathy, uveitis, infective dermatitis, and polymyositis. The mechanism by which the virus causes disease is still unknown. HTLV- 1 infection has been reported in many regions of the world but is most prevalent in Southern Japan, the Caribbean basin, Central and West Africa, the Southeastern United States, Melanesia, parts of South Africa, the Middle East and India. Approximately 30 million people are infected by HTLV-1 worldwide, although only 3-5% of the infected individuals evolve Adult T-cell Leukemia (ATL) during their life and the prognosis for those infected is still poor. The retroviral proteases (PRs) are essential for viral replication because they process viral Gag and Gag-(Pro)-Pol polyproteins during maturation, much like the PR from Human Immunodeficiency Virus-1 (HIV-1). Various antiviral inhibitors are in clinical use and one of the most significant classes is HIV-1 PR inhibitors, which have used for antiretroviral therapy in the treatment of AIDS. HTLV-1 PR and HIV-1 PR are homodimeric aspartic proteases with 125 and 99 residues, respectively. Even though substrate specificities of these two enzymes are different, HTLV-1 PR shares 28% similarity with HIV-1 PR overall and the substrate binding sites have 45% similarity. In addition to the 125-residue full length HTLV-1 PR, constructs with various C- terminal deletions (giving proteases with lengths of 116, 121, or 122 amino acids) were made in order to elucidate the effect of the residues in the C-terminal region. It was suggested that five amino acids in the C-terminal region are not necessary for the enzymatic activity in Hayakawa et al. 1992. In 2004 Herger et al. had suggested that 10 amino acids at the C-terminal region are not necessary for catalytic activity. A recent paper suggested that C-terminal residues are essential; and that catalytic activity lowers upon truncation, with even the last 5 amino acids necessary for full catalytic activity (1). The mutation L40I has been made to prevent autoproteolysis and the W98V mutation was made to make the active site of HTLV-1 PR similar to HIV-1 PR. We have characterized C-terminal amino acids of HTLV-1 PR as not being essential for full catalytic activity. We have discovered potential new inhibitors by in silico screening of 116-HTLV-1 PR. These small molecules were tested kinetically for various constructs including the 116, 121 and 122-amino acid forms of HTLV-1 PR. Inhibitors with the best inhibition constants were used in HTLV-1 infected cells and one of the inhibitors seems to inhibit gag processing.
369

Importance of the Structural Components of C-linked Glycopeptides to Specific-antifreeze Activity: From Glycopeptides to Small Molecule Inhibitors of Ice Recrystallization

Trant, John F. 22 February 2012 (has links)
One of the largest problems in current medicine is the shortage of organs for transplant due to technological limitations in the storage of organs for any length of time. A possible solution to this problem would involve cryopreservation. However, current cryopreservatives such as sucrose or DMSO have concerning cytotoxic issues that limit their possible applications. A major cause of cryoinjury is the uncontrolled recrystallization of inter and intra-cellular ice crystals that occurs during the thawing process leading to mechanical damage and dehydration. The Ben lab has thus been interested in the design of compounds that are capable of inhibiting this process but do not possess other undesirable properties found in the native compounds. These synthetic analogues have been shown to increase cellular viability post-thaw. A series of mixed α/β glycopeptides are prepared and analyzed for antifreeze properties. The results of this study imply that it is not the gross conformation of the glycopeptide that is responsible for activity, but rather that intramolecular relationships may be responsible for disrupting the reorganization of ice. A technique was devised for the incorporation of triazoles into the analogues to investigate the importance of the linker and to greatly simplify the synthesis of a library of glycoconjugates. It was found that the IRI activity of glycopeptides is very sensitive to the distance between carbohydrate and peptide backbone. The electron density at the anomeric oxygen is an important parameter with respect to intramolecular networks. A series of substituted galactosides is presented that modify the electronics of the anomeric oxygen. The results demonstrate that decreasing electron density at this position appears to improve IRI activity in a predictable manner. To better understand the remarkable IRI activity of a key analogue, it was systematically truncated. This study led to the serendipitous discovery of a series of very highly IRI active analogues that do not contain a peptide backbone. These compounds represent the first non-glycopeptides that can show very significant IRI activity even at very low concentrations. The final portion of the thesis reports the efforts towards the preparation of a carbasugar analogue of AFGP-8.
370

Precise Size Control and Noise Reduction of Solid-state Nanopores for the Detection of DNA-protein Complexes

Beamish, Eric 07 December 2012 (has links)
Over the past decade, solid-state nanopores have emerged as a versatile tool for the detection and characterization of single molecules, showing great promise in the field of personalized medicine as diagnostic and genotyping platforms. While solid-state nanopores offer increased durability and functionality over a wider range of experimental conditions compared to their biological counterparts, reliable fabrication of low-noise solid-state nanopores remains a challenge. In this thesis, a methodology for treating nanopores using high electric fields in an automated fashion by applying short (0.1-2 s) pulses of 6-10 V is presented which drastically improves the yield of nanopores that can be used for molecular recognition studies. In particular, this technique allows for sub-nanometer control over nanopore size under experimental conditions, facilitates complete wetting of nanopores, reduces noise by up to three orders of magnitude and rejuvenates used pores for further experimentation. This improvement in fabrication yield (over 90%) ultimately makes nanopore-based sensing more efficient, cost-effective and accessible. Tuning size using high electric fields facilitates nanopore fabrication and improves functionality for single-molecule experiments. Here, the use of nanopores for the detection of DNA-protein complexes is examined. As proof-of-concept, neutravidin bound to double-stranded DNA is used as a model complex. The creation of the DNA-neutravidin complex using polymerase chain reaction with biotinylated primers and subsequent purification and multiplex creation is discussed. Finally, an outlook for extending this scheme for the identification of proteins in a sample based on translocation signatures is presented which could be implemented in a portable lab-on-a-chip device for the rapid detection of disease biomarkers.

Page generated in 0.0419 seconds