Fakultät für Chemie und Pharmazie - Digitale Hochschulschriften der LMU - Teil 06/06

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Ludwig-Maximilians-Universität München

  • May 10, 2016 LATEST EPISODE
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High-quality, high-throughput measurement of protein-DNA binding using HiTS-FLIP

Play Episode Listen Later May 10, 2016


In order to understand in more depth and on a genome wide scale the behavior of transcription factors (TFs), novel quantitative experiments with high-throughput are needed. Recently, HiTS-FLIP (High-Throughput Sequencing-Fluorescent Ligand Interaction Profiling) was invented by the Burge lab at the MIT (Nutiu et al. (2011)). Based on an Illumina GA-IIx machine for next-generation sequencing, HiTS-FLIP allows to measure the affinity of fluorescent labeled proteins to millions of DNA clusters at equilibrium in an unbiased and untargeted way examining the entire sequence space by Determination of dissociation constants (Kds) for all 12-mer DNA motifs. During my PhD I helped to improve the experimental design of this method to allow measuring the protein-DNA binding events at equilibrium omitting any washing step by utilizing the TIRF (Total Internal Reflection Fluorescence) based optics of the GA-IIx. In addition, I developed the first versions of XML based controlling software that automates the measurement procedure. Meeting the needs for processing the vast amount of data produced by each run, I developed a sophisticated, high performance software pipeline that locates DNA clusters, normalizes and extracts the fluorescent signals. Moreover, cluster contained k-mer motifs are ranked and their DNA binding affinities are quantified with high accuracy. My approach of applying phase-correlation to estimate the relative translative Offset between the observed tile images and the template images omits resequencing and thus allows to reuse the flow cell for several HiTS-FLIP experiments, which greatly reduces cost and time. Instead of using information from the sequencing images like Nutiu et al. (2011) for normalizing the cluster intensities which introduces a nucleotide specific bias, I estimate the cluster related normalization factors directly from the protein Images which captures the non-even illumination bias more accurately and leads to an improved correction for each tile image. My analysis of the ranking algorithm by Nutiu et al. (2011) has revealed that it is unable to rank all measured k-mers. Discarding all the clusters related to previously ranked k-mers has the side effect of eliminating any clusters on which k-mers could be ranked that share submotifs with previously ranked k-mers. This shortcoming affects even strong binding k-mers with only one mutation away from the top ranked k-mer. My findings show that omitting the cluster deletion step in the ranking process overcomes this limitation and allows to rank the full spectrum of all possible k-mers. In addition, the performance of the ranking algorithm is drastically reduced by my insight from a quadratic to a linear run time. The experimental improvements combined with the sophisticated processing of the data has led to a very high accuracy of the HiTS-FLIP dissociation constants (Kds) comparable to the Kds measured by the very sensitive HiP-FA assay (Jung et al. (2015)). However, experimentally HiTS-FLIP is a very challenging assay. In total, eight HiTS-FLIP experiments were performed but only one showed saturation, the others exhibited Protein aggregation occurring at the amplified DNA clusters. This biochemical issue could not be remedied. As example TF for studying the details of HiTS-FLIP, GCN4 was chosen which is a dimeric, basic leucine zipper TF and which acts as the master regulator of the amino acid starvation Response in Saccharomyces cerevisiae (Natarajan et al. (2001)). The fluorescent dye was mOrange. The HiTS-FLIP Kds for the TF GCN4 were validated by the HiP-FA assay and a Pearson correlation coefficient of R=0.99 and a relative error of delta=30.91% was achieved. Thus, a unique and comprehensive data set of utmost quantitative precision was obtained that allowed to study the complex binding behavior of GCN4 in a new way. My Downstream analyses reveal that the known 7-mer consensus motif of GCN4, which is TGACTCA, is modulated by its 2-mer neighboring flanking regions spanning an affinity range over two orders of magnitude from a Kd=1.56 nM to Kd=552.51 nM. These results suggest that the common 9-mer PWM (Position Weight Matrix) for GCN4 is insufficient to describe the binding behavior of GCN4. Rather, an additional left and right flanking nucleotide is required to extend the 9-mer to an 11-mer. My analyses regarding mutations and related delta delta G values suggest long-range interdependencies between nucleotides of the two dimeric half-sites of GCN4. Consequently, models assuming positional independence, such as a PWM, are insufficient to explain these interdependencies. Instead, the full spectrum of affinity values for all k-mers of appropriate size should be measured and applied in further analyses as proposed by Nutiu et al. (2011). Another discovery were new binding motifs of GCN4, which can only be detected with a method like HiTS-FLIP that examines the entire sequence space and allows for unbiased, de-novo motif discovery. All These new motifs contain GTGT as a submotif and the data collected suggests that GCN4 binds as monomer to these new motifs. Therefore, it might be even possible to detect different binding modes with HiTS-FLIP. My results emphasize the binding complexity of GCN4 and demonstrate the advantage of HiTS-FLIP for investigating the complexity of regulative processes.

Structural und functional characterization of Rubisco assembly chaperones

Play Episode Listen Later Apr 28, 2016


In the present study, the structure and mechanism of two assembly chaperones of Rubisco, Raf1 and RbcX, were investigated. The role of Raf1 in Rubisco assembly was elucidated by analyzing cyanobacterial and plant Raf1 with a vast array of biochemical and biophysical techniques. Raf1 is a dimeric protein. The subunits have a two-domain structure. The crystal structures of two separate domains of Arabidopsis thaliana (At) Raf1 were solved at resolutions of 1.95 Å and 2.6–2.8 Å, respectively. The oligomeric state of Raf1 proteins was investigated by size exclusion chromatography connected to multi angle light scattering (SEC-MALS) and native mass spectrometry (MS). Both cyanobacterial and plant Raf1 are dimeric with an N-terminal domain that is connected via a flexible linker to the C-terminal dimerization domain. Both Raf1 poteins were able to promote assembly of cyanobacterial Rubisco in an in vitro reconstitution system. The homologous cyanobacterial system resulted in very high yields of active Rubisco (>90%), showing the great efficiency of Raf1 mediated Rubisco assembly. Two distinct oligomeric complex assemblies in the assembly reaction could be identified via native PAGE immunoblot analyses as well as SEC-MALS and native MS. Furthermore, a structure-guided mutational analysis of Raf1 conserved residues in both domains was performed and residues crucial for Raf1 function were identified. A new model of Raf1 mediated Rubisco-assembly could be proposed by analyzing the Raf1-Rubisco oligomeric complex with negative stain electron microscopy. The final model was validated by determining Raf1-Rubisco interaction sites using chemical crosslinking in combination with mass spectrometry. Taken together, Raf1 acts downstream of chaperonin-assisted Rubisco large subunit (RbcL) folding by stabilizing RbcL antiparallel dimers for assembly into RbcL8 complexes with four Raf1 dimers bound. Raf1 displacement by Rubisco small subunit (RbcS) results in holoenzyme formation. In the second part of this thesis, the role of eukaryotic RbcX proteins in Rubisco assembly was investigated. Eukaryots have two distinct homologs of RbcX, RbcX-I and RbcX-II. Both, plant and algal RbcX proteins were found to promote cyanobacterial Rubisco assembly in an in vitro reconstitution system. Mutation of a conserved residue important for Rubisco assembly in cyanobacterial RbcX also abolished assembly by eukaryotic RbcX, underlining functional similarities among RbcX proteins from different species. The crystal structure of Chlamydomonas reinhardtii (Cr) RbcX was solved at a resolution of 2.0 Å. RbcX forms an arc-shaped dimer with a central hydrophobic cleft for binding the C-terminal sequence of RbcL. Structural analysis of a fusion protein of CrRbcX and the C-terminal peptide of RbcL suggests that the peptide binding mode of CrRbcX may differ from that of cyanobacterial RbcX. RbcX homologs appear to have adapted to their cognate Rubisco clients as a result of co-evolution. Preliminary analysis of RbcX in Chlamydomonas indicated that the protein functions as a Rubisco assembly chaperone in vivo. Therefore, RbcX was silenced using RNAi in Chlamydomonas which resulted in a photosynthetic growth defect in several transformants when grown under light. RbcX mRNA levels were highly decreased in these transformants which resulted in a concomitant decrease of Rubisco large subunit levels. Biochemical and structural analysis from both independent studies in this thesis show that Raf1 and RbcX fulfill similar roles in Rubisco assembly, thus suggesting that functionally redundant factors ensure efficient Rubisco biogenesis.

Chemical synthesis and enzymatic incorporation of artificial nucleotides

Play Episode Listen Later Apr 18, 2016


Deutsche Übersetzung des Titels: Chemische Synthese und enzymatischer Einbau von künstlichen Nukleotiden

Benzoxazepine-type inhibitors for the CBP/p300 bromodomains

Play Episode Listen Later Apr 15, 2016


Fri, 15 Apr 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19393/ https://edoc.ub.uni-muenchen.de/19393/1/Popp_Tobias_Alexander.pdf Popp, Tobias Alexander ddc:540, ddc:500, Fakultät für Chemie und Pharmazie

Mineralizer-assisted high-pressure high-temperature synthesis and characterization of novel phosphorus nitride imides and luminescent alkaline earth metal (oxo)nitridophosphates

Play Episode Listen Later Apr 11, 2016


Mon, 11 Apr 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19343/ https://edoc.ub.uni-muenchen.de/19343/1/Marchuk_Alexey.pdf Marchuk, Alexey

High pressure and microwave based synthesis of transition metal pnictides

Play Episode Listen Later Apr 11, 2016


Mon, 11 Apr 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19353/ https://edoc.ub.uni-muenchen.de/19353/1/Pobel_Roman.pdf Pobel, Roman ddc:540, ddc:500, Fakultät für Chemie und Pharmaz

Molecular mechanisms of PAH function in response to phenylalanine and tetrahydrobiopterin binding

Play Episode Listen Later Mar 17, 2016


Phenylketonuria (PKU) is an autosomal recessive inborn error of metabolism (IEM) caused by mutations in the phenylalanine hydroxylase (PAH) gene. The molecular mechanism underlying deficiency of the PAH protein is, in most of the cases, loss of function due to protein misfolding. PAH mutations induce disturbed oligomerisation, decreased stability and accelerated degradation of hepatic PAH, a key enzyme in phenylalanine metabolism. Since the development of a phenylalanine-restricted diet in the 1950ies, PKU is a prototype for treatable inherited diseases. About 60 years later, the natural PAH cofactor tetrahydrobiopterin (BH4) was shown to act as a pharmacological chaperone stabilising the misfolded PAH protein. In consequence, BH4 (KUVAN®) was introduced to the pharmaceutical market as an alternative treatment for BH4-responsive PAH deficiency. Therefore, PKU is also regarded as a prototype for a pharmacologically treatable protein misfolding disease. Despite the progress in PKU therapy, knowledge on the molecular basis of PKU and the BH4 mode of action was still incomplete. Biochemical and biophysical characterisation of purified variant PAH proteins, which were derived from patient’s mutations, aimed at a better understanding of the molecular mechanisms of PAH loss of function. We showed that local side-chain replacements induce global conformational changes with negative impact on molecular motions that are essential for physiological enzyme function. The development of a continuous real-time fluorescence-based assay of PAH activity allowed for robust analysis of steady state kinetics and allosteric behaviour of recombinantly expressed PAH proteins. We identified positive cooperativity of the PAH enzyme towards BH4, where cooperativity does not rely on the presence of phenylalanine but is determined by activating conformational rearrangements. In vivo investigations on the mode-of-action of BH4 revealed differences in pharmacodynamics but not in pharmacokinetics between different strains of PAH-deficient mice (wild-type, Pahenu1/1 and Pahenu1/2). These observations pointed to a significant impact of the genotype on responsiveness to BH4. The available database information on PAH function associated with PAH mutations was based on non-standardised enzyme activity assays performed in different cellular systems and under different conditions usually focusing on single PAH mutations. These inconsistent data on PAH enzyme activity hindered robust prediction of the patient’s phenotype. Furthermore, assays on single PAH mutations do not reflect the high allelic and phenotypic heterogeneity of PKU with 89 % of patients being compound heterozygotes. In addition, the knowledge on enzyme function and regulation in the therapeutic and pathologic metabolic context was still scarce. In order to get more insight into the interplay of the PAH genotype, the phenylalanine concentration and BH4 treatment, we performed functional analyses of both, single, purified PAH variants as well as PAH full genotypes in the physiological, pathological and therapeutic context. The analysis of PAH activity as a function of phenylalanine and BH4 concentrations enabled determination of the optimal working ranges of the enzyme and visualisation of differences in the regulation of PAH activity by BH4 and phenylalanine depending on the underlying genotype. Moreover, these PAH activity landscapes allowed for setting rules for dietary regimens and pharmacological treatment based on the genotype of the patient. Taken together, precise knowledge on the mechanism of the misfolding-induced loss of function in PAH deficiency enabled a better understanding of the molecular mode of action of pharmacological rescue of enzyme function by BH4. We implemented the combination of genotype-specific functional analyses together with biochemical, clinical and therapeutic data of individual patients as a powerful tool for phenotype prediction and paved the way for personalised medicine strategies in phenylketonuria.

The role of FKBP5 in transcriptional regulation and in shaping cellular pathways of psychopharmaca action

Play Episode Listen Later Mar 10, 2016


FK506 binding protein 5 (FKBP5) has been linked to stress related diseases and treatment response in depression (Binder et al., 2004). The corresponding protein FKBP51 was first identified as co-chaperone of HSP90 in a complex with steroid hormone receptors, where it diminishes hormone affinity and nuclear translocation efficiency of the receptors (Pratt and Toft, 1997; Wochnik et al., 2005). With FKBP5 transcription being induced by glucocorticoid signalling, an ultra-short feedback loop is provided for regulation and termination of GR activity. Dysregulation of this ultra-short feedback loop interferes with the stress hormone regulation and likely contributes to the association of FKBP5 with stress-related psychiatric disorders. Recently, important actions of FKBP51 beyond glucocorticoid signalling have been characterised in shaping the posttranslational regulation of certain molecular pathways in response to treatment with particular psychopharmaca (Gassen et al., 2014, 2015). As a contribution to elucidating the role of FKBP5 in stress related diseases, a two-sided approach was taken in this study by analysing the role of FKBP5 in regulation of transcription and in calibrating the responsiveness of these pathways to psychopharmacological treatment. To elucidate the transcriptional effects of FKBP5 in an unbiased approach, the expression profile of mice with deleted FKBP5 and their litter mates with functional FKBP5 were compared. A marked difference in glyoxalase-1 (GLO1) transcription was observed with higher GLO1 transcription in mice with deleted FKBP5, which was reflected by about two-fold more GLO1 protein in these mice. The efforts in deciphering the role of FKBP5 in elevation of GLO1 expression led to the identification of a duplication of the GLO1 gene inherent to mice with deleted FKBP5; this likely explains the enhanced GLO1 expression in these mice. This observation exemplifies the flanking gene problem and is a note of caution for interpreting data from conventionally generated knock-out mice. Overall, deletion of FKBP5 did not markedly change gene expression. In the second part of this thesis, the molecular effects of psychopharmacologic drugs were profiled for their dependency on FKBP51 function to modulate intracellular pathways relevant for treatment outcome in a cellular FKBP5 knockout model. For this purpose, psychopharmaca from the classes of SSRIs, SSNRIs, TCAs, atypical antidepressants, mood stabilisers, and NMDA receptor antagonists were analysed. In addition to GSK3β and AKT, which were reported to interact with and be targeted by FKBP51 recently (Gassen et al., 2015; Pei et al., 2009), ERK was identified as a novel kinase interacting with and being targeted by FKBP51 in this work. With GSK3β, AKT, and ERK, three major kinases were observed to be regulated by psychopharmaca. The effects were not homogeneous across all psychopharmaca and only loosely followed drug classes. Moreover, regulation of these kinases as well as their downstream targets was non-uniformly influenced by FKBP51. With FKBP51 being a stress induced gene, this transcriptional mechanism efficiently links the stress response to the regulation of the targets analysed in this work. Moreover, markers of autophagy, a cellular degradation process which has been linked to neurotransmission, were detected to be regulated by valproic acid (VPA), a mood stabiliser with HDAC inhibitory activity. VPA, as well as a second HDAC inhibitor butyric acid (BUT) enhanced the transcription of late and delayed autophagy markers controlled by FOXO3 signalling. Considering the versatile action of FKBP51 on targets analysed in this work, the list of proteins modulated by FKBP5 seems by far not complete. The diversity of effects evoked by different psychopharmaca hints to superimposed molecular effects underlying treatment outcome. Better understanding of pathway responsiveness could yield molecular markers for personalised medication that could be utilised to improve treatment outcome in stress related psychiatric diseases.

Entwicklung von Triazolobenzotriazepinen und Triazolothienotriazepinen als selektive Inhibitoren von Bromodomänen der BET-Familie

Play Episode Listen Later Mar 4, 2016


Fri, 4 Mar 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19229/ https://edoc.ub.uni-muenchen.de/19229/1/Ratzke_Elfrun_A.pdf Ratzke, Elfrun Almuth

Molecular characterization of the interaction between peripherin-2 and opsins in rod and cone photoreceptors

Play Episode Listen Later Feb 24, 2016


The tetraspanin peripherin-2 is a glyco-membrane protein exclusively expressed in the outer segments of rod and cone photoreceptors. Mutations in peripherin-2 are associated with retinal disorders characterized by Degeneration of rod or cone cells. Previous unpublished work identified peripherin-2 as a potential novel part of the protein complex comprising the B-subunit of the cyclic nucleotide-gated channel (CNGB1a and the light detector rhodopsin. In the first part of this study, using a combination of protein biochemical and FRET approaches in transfected HEK293 cells and in virally transduced murine rod outer segments, it could be demonstrated that peripherin-2 simultaneously binds to both, CNGB1a and rhodopsin. The interaction between peripherin-2 and rhodopsin was not described in previous studies. The binding domain mediating the peripherin-2/rhodopsin interaction could be narrowed down to the fourth transmembrane domain (TM4) of peripherin-2. Finally, the data revealed that the G266D point mutation in TM4 of peripherin-2 that is linked to a rod degenerative disease selectively disrupts the peripherin-2/rhodopsin interaction. To analyze if peripherin-2 also binds to cone opsins in the second part of this study, a similar experimental approach was conducted as used for the investigation of the peripherin-2/rhodopsin interaction. In this context, it was unveiled that peripherin-2 binds to both, short wavelength-and medium wavelength-sensitive cone opsin (S-opsin and M-opsin, respectively) in transfected HEK293 cells and in outer segments of transduced murine cones. Co-immunoprecipitation and quantitative FRET analysis revealed that binding of peripherin-2 to M-opsin was stronger than the peripherin-2/S-opsin interaction. This result was supported by transmission electron microscopy studies using gold particles coupled to opsin- and peripherin-2-specific antibodies. Finally, quantitative FRET analysis in transfected HEK293 cells and in transduced cone outer segments demonstrated that the V268I Point mutation in TM4 of peripherin-2 associated with a degenerative cone disease significantly attenuates the peripherin-2/M-opsin interaction. Taken together, this study provides a proof-of-principle for FRET-based analysis of protein-protein interactions in the outer segments of rod and cone photoreceptors. This approach led to the identification of hitherto unknown Protein complexes between peripherin-2 and opsins suggesting a novel physiological role of peripherin-2 in rods and cones. Finally, Analysis of disease-linked point mutations unveiled the molecular determinants of the peripherin-2/opsin interaction. These results might contribute to understanding the differential penetrance of certain point mutations in rods and cones.

Assembly and optimization of a super-resolution STORM microscope for nanoscopic imaging of biological structures

Play Episode Listen Later Feb 18, 2016


Fluorescence microscopy is a widely used technique for imaging of biological structures due to its noninvasiveness although resolution of conventional fluorescence microscopes is limited to about 200-300 nm due to the diffraction limit of light. Super-resolution fluorescence microscopy offers an extension of the original method that allows optical imaging below the diffraction limit. In this thesis, a microscope for localization-based super-resolution fluorescence microscopy techniques such as Stochastic Optical Reconstruction Microscopy (STORM) or Photoactivated Localization Microscopy (PALM) was established. An epifluorescence microscope was built for this purpose that provides both widefield and Total Internal Reflection Fluorescence (TIRF) excitation modalities and focus was put on the special requirements of localization-based super-resolution methods. This included a high mechanical and optical stability realized by a compact design and implementation of a home-built perfect focus system. The setup was further designed to allow both two- and three-dimensional imaging. The work also included both the development of a setup control software and a software for the analysis of the required data. Different analysis methods and parameters were tested on simulated data before the performance of the microscope was demonstrated in two and three dimensions at appropriate test samples such as the cellular microtubule network. These experiments showed the capability of super-resolution microscopy to reveal underlying structures that cannot be resolved by conventional fluorescence microscopy. Resolutions could be achieved down to approximately 30 nm in the lateral and 115 nm in the axial dimension. Subsequently, the established method was applied to two biological systems. The first is a study of the budding of the human immunodeficiency virus type 1 (HIV-1) from the host cell. In this step of the viral reproduction cycle, the virus hijacks the cellular endosomal sorting complex required for transport (ESCRT) machinery to achieve membrane fission. ESCRT consists of the subcomplexes ESCRT-0, -I, -II and -III and additional related proteins, from which HIV-1 recruits certain components. The fission process is initiated by the HIV-1 Gag protein, which recruits the ESCRT-I protein Tsg101 and the ESCRT-related protein ALIX to the virus assembly site. Subsequently, ESCRT-III proteins CHMP4 and CHMP2 form transient lattices at the membrane, which are actively involved in membrane fission. However, the actual geometry of the ESCRT machinery assembling at the HIV-1 budding site that is driving the fission process is still not fully understood. Different models proposed either constriction of the budding neck by lattices surrounding the neck, by ESCRT structures within the neck or within the bud itself. A problematic aspect in previous studies was the usage of modified, tagged versions of the involved proteins for visualization. In this study, super-resolution microscopy was therefore applied to endogenous Tsg101, ALIX and CHMP2 isoform CHMP2A and to a version of CHMP4 isoform CHMP4B with a small HA-tag to elucidate the size and the distribution of the structure relative to the HIV-1 assembly sites. ESCRT structures colocalizing with HIV-1 exhibited closed, circular structures with an average size restricted to 45 and 60 nm in diameter. This size was significantly smaller than found for HIV-1 assembly sites and the constriction of the size, which was not observed for non-colocalizing ESCRT structures at the cell membrane, ruled out an external restriction model. Super-resolution imaging of ALIX often revealed an additional cloud-like structure of individual molecules surrounding the central clusters. This was attributed to ALIX molecules incorporated into the nascent HIV-1 Gag shell. Together with experiments that confirmed the non-physiological behavior of tagged Tsg101 and a relative orientation of ESCRT clusters towards the edge of the assembly site, the results strongly point toward a within-neck model. A second project focused on the influence of external constriction on cell migration. The latter plays an important role in various processes in the human body ranging from wound healing to metastasis formation by cancer cells. Migration is driven by the lamellipodium, which is a meshwork of fine actin filaments that drive membrane protrusion. Endothelial cells were grown on micropatterns that confined the freedom of movement of the cells. Three-dimensional super-resolution imaging revealed that the lamellipodia of these cells showed a much broader axial extension than was the case for control cells that grew without confinement of migration. The different organization of the actin filament network showed a clear effect of environmental conditions on cellular migration. Overall, it was possible to build a super-resolution fluorescence microscope over the course of this study and establish the required analysis methods to allow STORM and PALM imaging below the diffraction limit of light. Two applications further showed that these tools are capable of answering currently discussed questions in the biological sciences.

Artificial angiogenesis

Play Episode Listen Later Feb 17, 2016


Wed, 17 Feb 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19241/ https://edoc.ub.uni-muenchen.de/19241/1/Kick_Kerstin.pdf Kick, Kerstin ddc:540, ddc:500, Fakultät für Chemie und Pharmazie 0

Models for angiogenesis on micro-structured surfaces

Play Episode Listen Later Feb 15, 2016


Endothelial cell (EC) migration is an essential process in angiogenesis as ECs sprout from preexisting vessels, following chemotactic gradients. However, most of the data obtained about EC migration has been acquired in artificial two dimensional (2D) cell culture environments. Recent reports showed that migration in fibrillary environments can be mimicked by spatial confinement, achieved by micro patterning techniques (Doyle et al. 2009). In the first part of this work it was investigated whether a model system based on linearly structured surfaces allows to draw conclusions about the migration of ECs in fibrillary 3D collagen matrices. In order to estimate the cellular behavior of ECs on linearly structured surfaces, a comprehensive cell biological analysis was performed. ECs on narrow 3 µm wide tracks (also termed 1D in the following) migrated less efficient in comparison to ECs on broader tracks in regard to mean velocity, persistence, and run velocity. Additionally, ECs in 1D displayed a distinct actin cytoskeleton architecture, compressed nuclei, and different orientation of the centrosome in comparison to ECs on wider tracks. The frequent directional changes of ECs on narrow tracks were accompanied by pronounced membrane blebbing, while migrating and elongated cells displayed a lamellipodium as cellular protrusion. This behavior was contractility-dependent as both modes were provoked by using Blebbistatin or Calyculin A, respectively. The comparison between 1D and 3D migrating cells revealed a striking similarity in actin cytoskeleton architecture and in switching between two morphological modes. Cells migrating in 3D moved slower but more persistent after Blebbistatin treatment, which was likewise the case for cells migrating in 1D. In contrast to this, cells in the 2D system migrated faster but less persistent after Blebbistatin treatment. A Rac1 inhibitor used in this study showed the tendency to influence the migratory potential similarly in 1D and 3D, in contrast to 2D. However, a microtubule disrupting agent displayed different effects in 1D and 3D. These experiments demonstrated that the 1D system allows to draw conclusions about certain aspects of 3D migration. Thus, using this 1D migration system, important aspects of 3D migration can be mimicked in a highly controlled setting. In the second part of this work, a system for artificial tip cell formation was investigated. For the analysis of tip and stalk cells specifically structured surfaces were designed. These structures provided areas allowing only a restricted number of cell-cell contacts and areas allowing a high number of cell-cell contacts. ECs with a low number of cell-cell contacts displayed increased VEGFR2 expression levels in comparison to cells with a high number of cell-cell contacts, a phenomenon which was inhibited by using a Notch signaling inhibitor. This system will be a useful tool in the future to decipher tip and stalk cell competition within a defined cellular population and a defined microscopic frame

Strukturelle Studien am Ribosom von P. falciparum, an ribosomalen Komplexenmit ERj1 und am translationsarretierten RNC mit XBP1

Play Episode Listen Later Feb 1, 2016


Mon, 1 Feb 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19111/ https://edoc.ub.uni-muenchen.de/19111/1/Hiekel_Anian.pdf Hiekel, Anian

Biochemical characterization of the Chp1 chromodomain binding to the nucleosome core and its role in heterochromatin formation

Play Episode Listen Later Feb 1, 2016


Eukaryotic genomes are organized inside the cell nucleus in a structured macromolecular DNA-protein polymer named chromatin, formed by single discrete unites called Nucleosomes. The packing of the genetic information into chromatin allows the efficient regulation of several nuclear processes, such as gene expression and transcription, DNA replication, cell cycle progression, chromosome segregation and DNA damage repair. Chromatin comes in two flavors: a transcriptionally active, more loosened state, called euchromatin and a transcriptionally silent or low expressed, more compact state, called heterochromatin. The assembly of silent chromatin or heterochromatin is fundamental for the regulation of every nuclear process and it is driven in most Eukaryotes by the deposition and the read-out of the histone H3 lysine 9 methylation (H3K9me) post-translational modification (PTM). H3K9me on the nucleosome is specifically bound by chromatin readers called chromodomains (CD) and this recognition is fundamental for the downstream processes that lead to the formation of heterochromatin and shut down the expression of single genes or entire gene clusters. Despite several studies have been done on different chromodomains binding to H3K9me histone tail peptides, to date there was no structural information on how chromodomains interact with their natural binding partners, the H3K9me3 Nucleosomes. In a preliminary structural study carried out in our laboratory we solved the cryo-electron microscopy (Cryo-EM) structure of the chromodomain of the fission yeast Chp1 protein (Chp1CD) in complex with an H3K9me nucleosome. The structure showed that the Chp1CD interacts not only with the histone H3 tail but also with the histone globular domains in the Nucleosome core, primarily with histone H3. Mutations in the residues of Chp1CD that form the binding interface with the Nucleosome core (two loops in the β-sheet of the domain) caused a drop of the affinity in vitro for the H3K9me Nucleosome, which was independent from the histone H3K9me tail interaction. Cells harboring the same Chp1CD loop mutations were defective in silencing centromeric transcripts and maintain the deposition of the H3K9me mark for heterochromatin formation. This indicated that Chp1CD-nucleosome core interaction is fundamental for heterochromatin formation in fission yeast and opened up to the possibility that chromodomains could read multiple histone PTMs, on both the recruiting histone tail and on the nucleosome core. This study substantially contributes to understand how chromodomains interact with chromatin, how much the nucleosome core interaction is conserved among different CDs and how different chromodomain proteins are regulated at the same loci. Understanding how chromodomain readers recognize nucleosomes is fundamental to uncover the basics of gene silencing and heterochromatin formation.

Energetic materials based on benzenes, 2,2'-bisimidazole and 1,2,4,5-tetrazines

Play Episode Listen Later Jan 26, 2016


Tue, 26 Jan 2016 12:00:00 +0100 https://edoc.ub.uni-muenchen.de/19146/ https://edoc.ub.uni-muenchen.de/19146/1/Preimesser_Andreas.pdf Preimesser, Andreas ddc:540, ddc:500, Fakultät für Chemie und P

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