406 research outputs found
Quantitative Determination of Natriuretic Peptides in Human Biological Samples with a Bioassay Using Cultured Cells
Peer Reviewe
Experimental Verification of the Chemical Sensitivity of Two-Site Double Core-Hole States Formed by an X-ray FEL
We have performed X-ray two-photon photoelectron spectroscopy (XTPPS) using
the Linac Coherent Light Source (LCLS) X-ray free-electron laser (FEL) in order
to study double core-hole (DCH) states of CO2, N2O and N2. The experiment
verifies the theory behind the chemical sensitivity of two-site (ts) DCH states
by comparing a set of small molecules with respect to the energy shift of the
tsDCH state and by extracting the relevant parameters from this shift.Comment: 11 pages, 2 figure
Quenching and restoring of the A 2Π cationic state in resonant Auger electron spectra of CO in the vicinity of the O 1s→2π resonance
X-ray absorption and resonant Auger spectroscopy of O2 in the vicinity of the O 1s→σ* resonance: Experiment and theory
Extreme Ultraviolet Wave Packet Interferometry of the Autoionizing HeNe Dimer
Femtosecond extreme ultraviolet wave packet interferometry (XUV-WPI) was applied to study resonant interatomic Coulombic decay (ICD) in the HeNe dimer. The high demands on phase stability and sensitivity for vibronic XUV-WPI of molecular-beam targets are met using an XUV phase-cycling scheme. The detected quantum interferences exhibit vibronic dephasing and rephasing signatures along with an ultrafast decoherence assigned to the ICD process. A Fourier analysis reveals the molecular absorption spectrum with high resolution. The demonstrated experiment shows a promising route for the real-time analysis of ultrafast ICD processes with both high temporal and high spectral resolution
Peptide substrate identification for yeast Hsp40 Ydj1 by screening the phage display library
We have identified a peptide substrate for molecular chaperone Hsp40 Ydj1 by utilizing the combination of phage display library screening and isothemol titration calirimetry (ITC). The initial peptide substrate screening for Hsp40 Ydj1 has been carried out by utilizing a 7-mer phage display library. The peptide sequences from the bio-panning were synthesized and object to the direct affinity measurement for Hsp40 Ydj1 by isothemol titration calirimetry studies. The peptide which has the measurable affinity with Ydj1 shows enriched hydrophobic residues in the middle of the substrate fragment. The peptide substrate specificity for molecular chaperone Hsp40 has been analyzed
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