Tuning the magnetic ground state of a novel tetranuclear Nickel(II) molecular complex by high magnetic fields

Electron spin resonance and magnetization data in magnetic fields up to 55 T of a novel multicenter paramagnetic molecular complex [L_2Ni_4(N_3)(O_2C Ada)_4](Cl O_4) are reported. In this compound, four Ni centers each having a spin S = 1 are coupled in a single molecule via bridging ligands (including a \mu_4-azide) which provide paths for magnetic exchange. Analysis of the frequency and temperature dependence of the ESR signals yields the relevant parameters of the spin Hamiltonian, in particular the single ion anisotropy gap and the g factor, which enables the calculation of the complex energy spectrum of the spin states in a magnetic field. The experimental results give compelling evidence for tuning the ground state of the molecule by magnetic field from a nonmagnetic state at small fields to a magnetic one in strong fields owing to the spin level crossing at a field of ~25 T.Comment: revised version, accepted for publication in Physical Review

Beziehungen zwischen inaktem Parathormon, Kalzium und Phosphat in Abhängigkeit vom Ausmaß der chronischen Niereninsuffizienz

Die chronische Niereninsuffizienz geht mit verschiedenartigen Veränderungen im Körper einher. Neben dem Magen-Darm-Trakt, dem Immunsystem, dem Herz-Kreislauf-System und vielen anderen Organsystemen, steht im Mittelpunkt meiner Arbeit die Veränderungen des Knochenstoffwechsels im Ausmaß der chronischen Niereninsuffizienz und die Entwicklung einer sekundäre Hyperparathyreoidismus. Das Ziel der Arbeit war es allein anhand von Laborparametern und unter Verzicht einen zugrundeliegenden Knochenmarksbiopsie den Zustand des Knochenstoffwechsels zu beurteilen. Es wurde nach Laborparametern gesucht, die in direktem Zusammenhang mit dem iPTH stehen und die Spiegel direkt beeinflussen. Wir haben uns zur Aufgabe gesetzt eine empirische Gleichung zu entwickeln anhand der man Schwellenwerte für das iPTH in den verschieden Stadien der chronischen Niereninsuffizienz allein durch einen klinisch-chemischen Parameter vorhersagen kann. Dazu wurden 291 Patienten in eine chronisch niereninsuffiziente und in eine Dialysegruppe unterteilt, retrospektiv anhand ihrer Nierenretention- und Knochenstoffwechselparameter analysiert, bezüglich ihrer Therapie verglichen und durch Pearson-Korrelationen statistisch signifikante Zusammenhänge ermittelt. Es gelang in dieser Arbeit vier signifikante Parameter zur Vorhersage von iPTH-Schwellenwerten zu ermitteln durch Aufstellung einer empirische Gleichung. Serumkreatinin stellte sich als signifikanteste Variable heraus. Es wurden des weiteren Vierfelderteste druchgeführt um die Sensitivität dieser Vorhersage zu ermitteln und die Nutzbarkeit im klinischen Alltag herauszustellen. Das Serumkreatinin kann als Vorhersage der iPTH-Spiegel genutzt werden und die ermittelten Schwellenwerte sollten das therapeutische Handeln beeinflussen

Role of endonucleases XPF and XPG in nucleotide excision repair of platinated DNA and cisplatin/oxaliplatin cytotoxicity

Resistance of tumor cells to platinum anticancer agents poses a major problem in cancer chemotherapy. One of the mechanisms associated with platinum-based drug resistance is the enhanced capacity of the cell to carry out nucleotide excision repair (NER) on platinum-damaged DNA. Endonucleases XPF and XPG are critical components of NER, responsible for excising the damaged DNA strand to remove the DNA lesion. Here, we investigated possible consequences of down-regulation of XPF and XPG gene expression in osteosarcoma cancer cells (U2OS) and the impact on cellular transcription and DNA repair. We further evaluated the sensitivity of such cells toward the platinum anticancer drugs cisplatin and oxaliplatin.National Cancer Institute (U.S.) (Grant Number CA034992.)National University of Singapore.German Academic Exchange Service (DAAD

Topologically tunable polaritons based on two-dimensional crystals in a photonic lattice

Topological photonics is an emergent research discipline which interlinks fundamental aspects of photonics, information processing and solid-state physics. Exciton-polaritons are a specifically interesting platform to study topological phenomena, since the coherent light matter coupling enables new degrees of freedom such as tunable non-linearities, chiralities and dissipation. Room-temperature operation of such exciton-polaritons relies on materials comprising both, large exciton binding energies and oscillator strength. We harness widely spectrally tunable, room temperature exciton-polaritons based on a WS2 monolayer in an open optical cavity to realize a polariton potential landscape which emulates the Su-Schrieffer-Heeger (SSH) Hamiltonian. It comprises a domain boundary hosting a topological, exponentially localized mode at the interface between two lattices characterized by different Zak-phases which features a spectral tunability over a range as large as 80 meV. Moreover, we utilize the unique tilt-tunability of our implementation, to transform the SSH-lattice into a Stark-ladder. This transformation couples the topologically protected defect mode to propagating lattice modes, and effectively changes the symmetry of the system. Furthermore, it allows us to directly quantify the Zak-phase difference $\Delta_{Zak}=(1.13\pm 0.11)\pi$ between the two topological phases. Our work comprises an important step towards in-situ tuning topological lattices to control and guide light on non-linear chips

Ultra-bright single photon source based on an atomically thin material

Solid-state single photon sources are central building blocks in quantum communication networks and on-chip quantum information processing. Atomically thin crystals were established as possible candidates to emit non-classical states of light, however, the performance of monolayer-based single photon sources has so far been lacking behind state-of-the-art devices based on volume crystals. Here, we implement a single photon source based on an atomically thin sheet of WSe2 coupled to a spectrally tunable optical cavity. It is characterized by a high single photon purity with a $g^{(2)}(0)$ value as low as $4.7 \pm 0.7 \%$ and a record-high first lens brightness of linearly polarized photons as large as $65 \pm 4 \%$. Interestingly, the high performance of our devices allows us to observe genuine quantum interference phenomena in a Hong-Ou-Mandel experiment. Our results demonstrate that open cavities and two-dimensional materials constitute an excellent platform for ultra-bright quantum light sources: the unique properties of such two-dimensional materials and the versatility of open cavities open an inspiring avenue for novel quantum optoelectronic devices.Comment: 12 pages, 7 figure

Synthesis of 2-Alkylideneisochromans by Cyclocarbonylative Sonogashira Reactions

In this study we used a tandem carbonylative Sonogashira reaction/cyclisation process to construct alkylidene-functionalized isochromans in high yields with complete stereoselectivity (only Z isomers were formed). The reaction was per-formed in the absence of a CuI co-catalyst with a small amount of PdCl2(PPh3)2 (0.2–0.5 mol-%), and aryl iodides bearing both electron-donating and electron-withdrawing substituents were successfully employe

Fluorescent probes for the analysis of DNA strand scission in base excision repair

We have developed fluorescent probes for the detection of strand scission in the excision repair of oxidatively damaged bases. They were hairpin-shaped oligonucleotides, each containing an isomer of thymine glycol or 5,6-dihydrothymine as a damaged base in the center, with a fluorophore and a quencher at the 5′- and 3′-ends, respectively. Fluorescence was detected when the phosphodiester linkage at the damage site was cleaved by the enzyme, because the short fragment bearing the fluorophore could not remain in a duplex form hybridized to the rest of the molecule at the incubation temperature. The substrate specificities of Escherichia coli endonuclease III and its human homolog, NTH1, determined by using these probes agreed with those determined previously by gel electrophoresis using 32P-labeled substrates. Kinetic parameters have also been determined by this method. Since different fluorophores were attached to the oligonucleotides containing each lesion, reactions with two types of substrates were analyzed separately in a single tube, by changing the excitation and detection wavelengths. These probes were degraded during an incubation with a cell extract. Therefore, phosphorothioate linkages were incorporated to protect the probes from nonspecific nucleases, and the base excision repair activity was successfully detected in HeLa cells

Paradoxes in carcinogenesis: New opportunities for research directions

<p>Abstract</p> <p>Background</p> <p>The prevailing paradigm in cancer research is the somatic mutation theory that posits that cancer begins with a single mutation in a somatic cell followed by successive mutations. Much cancer research involves refining the somatic mutation theory with an ever increasing catalog of genetic changes. The problem is that such research may miss paradoxical aspects of carcinogenesis for which there is no likely explanation under the somatic mutation theory. These paradoxical aspects offer opportunities for new research directions that should not be ignored.</p> <p>Discussion</p> <p>Various paradoxes related to the somatic mutation theory of carcinogenesis are discussed: (1) the presence of large numbers of spatially distinct precancerous lesions at the onset of promotion, (2) the large number of genetic instabilities found in hyperplastic polyps not considered cancer, (3) spontaneous regression, (4) higher incidence of cancer in patients with xeroderma pigmentosa but not in patients with other comparable defects in DNA repair, (5) lower incidence of many cancers except leukemia and testicular cancer in patients with Down's syndrome, (6) cancer developing after normal tissue is transplanted to other parts of the body or next to stroma previously exposed to carcinogens, (7) the lack of tumors when epithelial cells exposed to a carcinogen were transplanted next to normal stroma, (8) the development of cancers when Millipore filters of various pore sizes were was inserted under the skin of rats, but only if the holes were sufficiently small. For the latter paradox, a microarray experiment is proposed to try to better understand the phenomena.</p> <p>Summary</p> <p>The famous physicist Niels Bohr said "How wonderful that we have met with a paradox. Now we have some hope of making progress." The same viewpoint should apply to cancer research. It is easy to ignore this piece of wisdom about the means to advance knowledge, but we do so at our peril.</p

Association between XPF Polymorphisms and Cancer Risk: A Meta-Analysis

Background: Xeroderma pigmentosum complementation group F (XPF or ERCC4) plays a key role in DNA repair that protects against genetic instability and carcinogenesis. A series of epidemiological studies have examined associations between XPF polymorphisms and cancer risk, but the findings remain inconclusive. Methodology/Principal Findings: In this meta-analysis of 47,639 cancer cases and 51,915 controls, by searching three electronic databases (i.e., MEDLINE, EMBASE and CNKI), we summarized 43 case-control studies from 29 publications on four commonly studied polymorphisms of XPF (i.e., rs1800067, rs1799801, rs2020955 and rs744154), and we did not find statistical evidence of any significant association with overall cancer risk. However, in stratification analyses, we found a significant association of XPF-rs1799801 with a reduced cancer risk in Caucasian populations (4,845 cases and 5,556 controls; recessive model: OR = 0.87, 95% CI = 0.76–1.00, P = 0.049, P = 0.723 for heterogeneity test, I2 = 0). Further genotype-phenotype correlation analysis showed that the homozygous variant CC genotype carriers had higher XPF expression levels than that of the TT genotype carriers (Student’s t test for a recessive model: P = 0.046). No publication bias was found by using the funnel plot and Egger’s test. Conclusion: This meta-analysis suggests a lack of statistical evidence for the association between the four XPF SNPs and overall risk of cancers. However, XPF-rs1799801 may be associated with cancer risk in Caucasian populations, which needs to be further validated in single large, well-designed prospective studies