The Specific-Force Performance Parameter for Electromagnetic Launchers

A new electromagnetic-launcher (EML) performance parameter called the specific force is presented and analyzed in this paper. The specific force is the second derivative of the EML's force equation with respect to current and represents the force generated by the EML per unit square ampere, i.e., the EML's current efficiency. The specific force is independent of operating current and is defined for EMLs utilizing linear and nonlinear magnetic materials. The second derivative is termed as the specific force, since it unifies the various EML geometries so that only one force equation is required. The specific force, together with the energy-conversion efficiency, can be used as criterion to evaluate and compare EML geometries for various applications. The specific force for conventional railguns, augmented railguns, conventional helical launchers, and high-efficiency helical launchers is derived in this paper. The experimental performance of conventional railguns, augmented railguns, and conventional helical launchers are also analyzed in terms of their specific-force parameters.      

Ueber die Eigenschaften des Glycocolls

Ohne Zusammenfassung     

Entropic stabilization of tunable planar modulated superstructures

The self-assembly of novel [corrected] ordered structures with nanoparticles has recently received much attention. Here we use computer simulations to study a two-dimensional model system characterized by a simple isotropic interaction that could be realized with building blocks on the nanoscale. We find that the particles arrange themselves into hexagonal superstructures of twin boundaries whose superlattice vector can be tuned reversibly by changing the temperature. Thermodynamic stability is confirmed by calculating the free energy with a combination of thermodynamic integration and the Frenkel-Ladd method. Different contributions to the free energy difference are discussed.     

High-speed CH planar laser-induced fluorescence imaging using a multimode-pumped optical parametric oscillator

We report on high-speed CH planar laser-induced fluorescence (PLIF) imaging in turbulent diffusion flames using a multimode-pumped optical parametric oscillator (OPO). The OPO is pumped by the third-harmonic output of a multimode Nd:YAG cluster for direct signal excitation in the A-X (0,0) band of the CH radical. The lasing threshold, conversion efficiency, and linewidth are shown to depend on the number of pump passes in the ring cavity of the OPO. Single-shot CH PLIF images are acquired at 10 kHz with excitation energy up to 6 mJ/pulse at 431.1 nm. Signal-to-noise ratios of ~25-35 are the highest yet reported for high-speed CH PLIF.     

Single-shot ultrabroadband two-dimensional electronic spectroscopy of the light-harvesting complex LH2

Here we present two-dimensional (2D) electronic spectra of the light-harvesting complex LH2 from purple bacteria using coherent pulses with bandwidth of over 100 nm FWHM. This broadband excitation and detection has allowed the simultaneous capture of both the B800 and B850 bands using a single light source. We demonstrate that one laser pulse is sufficient to capture the entire 2D electronic spectrum with a high signal-to-noise ratio. At a waiting time of 800 fs, we observe population transfer from the B800 to B850 band as manifested by a prominent cross peak. These results will enable observation of the dynamics of biological systems across both ultrafast (<1 ps) and slower (>1 ms) timescales simultaneously.     

A semigroup characterization of well-posed linear control systems

We study the well-posedness of a linear control system Σ(A,B,C,D) with unbounded control and observation operators. To this end we associate to our system an operator matrix $\mathcal{A}$ on a product space $\mathcal{X}^{p}$ and call it p-well-posed if $\mathcal{A}$ generates a strongly continuous semigroup on $\mathcal{X}^{p}$ . Our approach is based on the Laplace transform and Fourier multipliers. The results generalize and complement those of Curtain and Weiss (Int. Ser. Numer. Math. vol. 91. Birkhäuser, Basel, 1989), Staffans and Weiss (Trans. Am. Math. Soc. 354:3229–3262, 2002) and are illustrated by a heat equation with boundary control and point observation.     

Directed evolution of cyclic peptides for inhibition of autophagy

In recent decades it has become increasingly clear that induction of autophagy plays an important role in the development of treatment resistance and dormancy in many cancer types. Unfortunately, chloroquine (CQ) and hydroxychloroquine (HCQ), two autophagy inhibitors in clinical trials, suffer from poor pharmacokinetics and high toxicity at therapeutic dosages. This has prompted intense interest in the development of targeted autophagy inhibitors to re-sensitize disease to treatment with minimal impact on normal tissue. We utilized Scanning Unnatural Protease Resistant (SUPR) mRNA display to develop macrocyclic peptides targeting the autophagy protein LC3. The resulting peptides bound LC3A and LC3B—two essential components of the autophagosome maturation machinery—with mid-nanomolar affinities and disrupted protein–protein interactions (PPIs) between LC3 and its binding partners in vitro. The most promising LC3-binding SUPR peptide accessed the cytosol at low micromolar concentrations as measured by chloroalkane penetration assay (CAPA) and inhibited starvation-mediated GFP-LC3 puncta formation in a concentration-dependent manner. LC3-binding SUPR peptides re-sensitized platinum-resistant ovarian cancer cells to cisplatin treatment and triggered accumulation of the adapter protein p62 suggesting decreased autophagic flux through successful disruption of LC3 PPIs in cell culture. In mouse models of metastatic ovarian cancer, treatment with LC3-binding SUPR peptides and carboplatin resulted in almost complete inhibition of tumor growth after four weeks of treatment. These results indicate that SUPR peptide mRNA display can be used to develop cell-penetrating macrocyclic peptides that target and disrupt the autophagic machinery in vitro and in vivo.

SUPR peptide mRNA display was used to evolve a cell-permeable, macrocyclic peptide for autophagy inhibition.