Reversible Live-Cell Labeling with Retro-engineered HaloTags Enables Long-Term High- and Super-Resolution Imaging

Self-labeling enzymes (SLE) such as the HaloTag have emerged as powerful tools in high and super-resolution fluorescence microscopy. Newly developed fluorogenic SLE substrates enable imaging in the presence of excess dye. To exploit this feature for reversible labeling, we engineered two variants of HaloTag7 with restored dehalogenase activity. Kinetic studies in vitro showed different turnover kinetics for reHaloTagS (≈0.006 s⁻¹) and reHaloTagF (≈0.055 s⁻¹). Imaging by confocal and stimulated emission depletion microscopy yielded 3-5-time enhanced photostability of reHaloTag labeling. Prominently, single molecule imaging with reHaloTags enabled controlled and stable labeling density over extended time periods. By combination with structured illumination, simultaneous visualization of single molecule diffusion and organellar dynamics was achieved. These applications highlight the potential of reHaloTag labeling for pushing the limits of advanced fluorescence microscopy techniques.     

Charged particle spectra in16O induced nuclear collisions at the CERN SPS

Charged particle multiplicity distributions and pseudo-rapidity density distributions from¹⁶O induced nuclear collisions at 200 and 60A GeV are presented. The data were taken, using a minimumbias trigger, with the WA80 set-up at the CERN SPS. In this presentation we focus on how the yield of charged particles depends on the projectile energy, the mass number of the target nucleus and the energy measured in a uranium-plastic sampling calorimeter covering angles close to zero degrees. The data are compared to simulations from the event generator FRITIOF.     

Tiling Convex Polygons with Congruent Equilateral Triangles

We study the sets $\mathcal{T}_{v}=\{m \in\{1,2,\ldots\}: \mbox{there is a convex polygon in }\mathbb{R}^{2}\mbox{ that has }v\mbox{ vertices and can be tiled with $m$ congruent equilateral triangles}\}$ , v=3,4,5,6. $\mathcal{T}_{3}$ , $\mathcal{T}_{4}$ , and $\mathcal{T}_{6}$ can be quoted completely. The complement $\{1,2,\ldots\} \setminus\mathcal{T}_{5}$ of $\mathcal{T}_{5}$ turns out to be a subset of Euler’s numeri idonei. As a consequence, $\{1,2,\ldots\} \setminus\mathcal{T}_{5}$ can be characterized with up to two exceptions, and a complete characterization is given under the assumption of the Generalized Riemann Hypothesis.     

Crystallographic report: Dimeric tetraphenyl‐1‐hydroxo‐3‐trifluoromethanesulfonatodistannoxane, [Ph2(HO)SnOSn(O3SCF3)Ph2]2

The molecular structure of the title compound, obtained by an adventitious phenyl group cleavage of Ph₃SnOSnPh₃ with triflic acid, reveals discrete centrosymmetric units of [Ph₂(HO)SnOSn(O₃SCF₃)Ph₂]₂ that are loosely associated via hydrogen bonding. Copyright © 2004 John Wiley & Sons, Ltd.     

Laser-Cooled Ions and Atoms in a Storage Ring

Hyperfine Interactions - We review recent experiments at the Heidelberg Test Storage Ring which apply advanced laser cooling techniques to stored ion beams. Very high phase-space densities are...     

Bose-einstein correlations in the target fragmentation region in 200A GeV16O+nucleus collisions

Correlations between positive pions are investigated in the target fragmentation region of 200A GeV¹⁶O+nucleus collisions. The pions are measured with the Plastic Ball detector in the WA80 experiment at the CERN SPS. The target mass dependence of the radii and the correlation strength extracted by interferometry is studied. A new approach to the fit of the correlation function is introduced. The correlation strength and both invariant and transverse radii increase with decreasing target mass. The transverse radius for¹⁶O+C reactions appears to be much larger than the geometrical radius of the nuclei involved. For the Au target only a small fraction of the measured pions contributes to the apparent correlation. Hints for a much larger second component in¹⁶O+Au reactions are observed. Rescattering phenomena may provide a clue to understand these phenomena.     

Methoxy and Methyl Group Rotation: Solid‐State NMR 1H Spin‐Lattice Relaxation,Electronic Structure Calculations,X‐ray Diffractometry,and Scanning Electron Microscopy

We report solid‐state ¹H nuclear magnetic resonance (NMR) spin‐lattice relaxation experiments, X‐ray diffractometry, field‐emission scanning electron microscopy, and both single‐molecule and cluster ab initio electronic structure calculations on 1‐methoxyphenanthrene ( 1 ) and 3‐methoxyphenanthrene ( 2 ) to investigate the rotation of the methoxy groups and their constituent methyl groups. The electronic structure calculations and the ¹H NMR relaxation measurements can be used together to determine barriers for the rotation of a methoxy group and its constituent methyl group and to develop models for the two coupled motions.