Post-sample aperture for low background diffraction experiments at X-ray free-electron lasers

The success of diffraction experiments from weakly scattering samples strongly depends on achieving an optimal signal-to-noise ratio. This is particularly important in single-particle imaging experiments where diffraction signals are typically very weak and the experiments are often accompanied by significant background scattering. A simple way to tremendously reduce background scattering by placing an aperture downstream of the sample has been developed and its application in a single-particle X-ray imaging experiment at FLASH is demonstrated. Using the concept of a post-sample aperture it was possible to reduce the background scattering levels by two orders of magnitude.Funding for this research was provided by: Deutsches Elektronen-Synchrotron; Deutsche Forschungsgemeinschaft (grant No. DFG-EXC1074); European Research Council (grant No. ERC614507-Kuepper); Helmholtz-Gemeinschaft (grant No. VI 419); Australian Research Council (grant No. DP170100131); National Science Foundation (grant No. STC-1231306)

Proteasome function is dispensable under normal but not under heat shock conditions in thermoplasma acidophilum

Hitherto the biology of proteolysis in prokaryotes, particularly in archaea, is only poorly understood. We hale used the tri-peptide vinyl sulfone inhibitor carboxybenzyl-leucyl-leucyl-leucine vinyl sulfone (Z-L-3 VS) to study the in vivo function of proteasomes in Thermoplasma acidophilum. Z-L-3 VS is a potent inhibitor of the Thermoplasma proteasome and is capable of modifying 75 to 80% of the proteasomal beta-subunits in cell cultures. Inhibition of proteasomes has only marginal effects under normal growth conditions. Under heat shock conditions, however, the effects of proteasome inhibition are much more severe, to the extent of complete cell growth arrest. These data suggest that other proteolytic systems may exist that can compensate for the loss of proteasome function in T. acidophilum. (C) 1998 Federation of European Biochemical Societies. [References: 25

Molecular Cloning, Sequence Analysis and Elicitor-/ozone-induced Accumulation of Cinnamyl Alcohol Dehydrogenase from Norway Spruce (<em>Picea abies </em>L.).

Cinnamyl alcohol dehydrogenase (CAD) is an enzyme involved in lignin biosynthesis. We have previously isolated pure CAD enzyme from Norway spruce (Picea abies L.) cell culture. Here we report on partial protein sequences of the 42 kDa CAD polypeptide. A cDNA encoding CAD was isolated from the spruce cell culture. The open reading frame of a full-length cDNA coded for a 357 amino acid polypeptide with a calculated M(r) of 38,777 Da. The identity of the deduced polypeptide was verified by comparison with amino acid sequences of tryptic peptides from the purified enzyme. Southern blot analysis showed the presence of only one gene for CAD. Sequence comparison with CAD from tobacco and with a N-terminal protein sequence from loblolly pine CAD showed an identity of 69.7% and 91.5%, respectively. Treatment of spruce cell cultures with elicitor, as well as of seedlings with ozone both markedly increased the CAD mRNA level