Towards a scalable quantum computer/simulator based on trapped ions

We describe the concept and experimental demonstration of the basic building blocks of a scalable quantum computer using trapped-ion qubits. The trap structure is divided into subregions where ion qubits can either be held as memory or subjected to individual rotations and multi-qubit gates in processor zones. Thus, ion qubits can become entangled in one trapping zone, then separated and distributed to separate zones (by switching control-electrode potentials) where subsequent single- and two-ion gates, and/or detection is performed. Recent work using these building blocks includes (1) demonstration of a dense-coding protocol, (2) demonstration of enhanced qubit-detection efficiency using quantum logic, (3) generation of GHZ states and their application to enhanced precision in spectroscopy, and (4) the realization of teleportation with atomic qubits. In the final section an analog quantum computer that could provide a shortcut towards quantum simulations under requirements less demanding than those for a universal quantum computer is also described. PACS 03.67.Lx; 32.80.Qk     

Spectral correlation in incommensurate multiwalled carbon nanotubes

We investigate the energy spectra of clean incommensurate double-walled carbon nanotubes, and find that the overall spectral properties are described by the critical statistics similar to that known in the Anderson metal-insulator transition. In the energy spectra, there exist three different regimes characterized by Wigner-Dyson, Poisson, and semi-Poisson distributions. This feature implies that the electron transport in incommensurate multiwalled nanotubes can be either diffusive, ballistic, or intermediate between them, depending on the position of the Fermi energy.     

Experimental indications for the response of the spectators to the participant blast

Precise momentum distributions of identified projectile fragments, formed in the reactions 238U+Pb and 238U+Ti at 1A GeV, are measured with a high-resolution magnetic spectrometer. With increasing mass loss, the velocities first decrease as expected from previously established systematics, then level off, and finally increase again. Light fragments are on the average even faster than the projectiles. This finding is interpreted as the response of the spectators to the participant blast. The reacceleration of projectile spectators is sensitive to the nuclear mean field and provides a new tool for investigating the equation of state of nuclear matter.     

Diffusion-limited extraction of organic ions by a track-membrane interfaced vacuum inlet

Glycerol-wetted track membranes (polyethylene terephthalate) were used to interface a low-vacuum facility (approximately (10(-3) Torr) to an ambient pressure liquid analyte. High-field charge extraction conditions were routinely maintained between the liquid samples and a grid collector. The latter was positioned just near to the vacuum-facing side of such membranes. Upon establishing a steady-state charge extraction regime, the collector currents were monitored and recorded at various solute concentration levels. The collector currents, which depend on solute concentration, were found to agree with recent theoretical treatments of such processes. Both positively- and negatively-charged species from organic solutions were routinely extracted. Ion injection for the low- and the high-mobility species has favored the diffusion-limited and the evaporation-limited schemes, respectively. Variable concentrations of 1-pyrenoyl-methylpyridinium bromide as well as naphthylacetic and anthracenecarboxylic acids in glycerol were used.     

Structural investigation of icosahedral Pd58.8U20.6Si20.6

The structure factors of the amorphous, icosahedral and crystalline Pd_58.8U_20.6Si_20.6 were measured with X-rays and neutrons. By comparing the radial distribution functions of the three phases, we find a similar short range order in the amorphous and icosahedral phase, but a different atomic arrangement in the crystalline phase. A magnetic long range order observed in the crystalline material is absent in the icosahedral phase.Dedicated to Professor Harry Thomas on the occasion of his 60th birthday     

Structure-function analysis of an enzymatic prenyl transfer reaction identifies a reaction chamber with modifiable specificity

Fungal indole prenyltransferases participate in a multitude of biosynthetic pathways. Their ability to prenylate diverse substrates has attracted interest for potential use in chemoenzymatic synthesis. The fungal indole prenyltransferase FtmPT1 catalyzes the prenylation of brevianamide F in the biosynthesis of fumitremorgin-type alkaloids, which show diverse pharmacological activities and are promising candidates for the development of antitumor agents. Here, we report crystal structures of unliganded Aspergillus fumigatus FtmPT1 as well as of a ternary complex of FtmPT1 bound to brevianamide F and an analogue of its isoprenoid substrate dimethylallyl diphosphate. FtmPT1 assumes a rare α/β-barrel fold, consisting of 10 circularly arranged β-strands surrounded by α-helices. Catalysis is performed in a hydrophobic reaction chamber at the center of the barrel. In combination with mutagenesis experiments, our analysis of the liganded and unliganded structures provides insight into the mechanism of catalysis and the determinants of regiospecificity. Sequence conservation of key features indicates that all fungal indole prenyltransferases possess similar active site architectures. However, while the dimethylallyl diphosphate binding site is strictly conserved in these enzymes, subtle changes in the reaction chamber likely allow for the accommodation of diverse aromatic substrates for prenylation. In support of this concept, we were able to redirect the regioselectivity of FtmPT1 by a single mutation of glycine 115 to threonine. This finding provides support for a potential use of fungal indole prenyltransferases as modifiable bioreactors that can be engineered to catalyze highly specific prenyl transfer reactions.