A novel multicollision induced dissociation scheme is employed to determine the energy content for mass-selected gallium cluster ions as a function of their temperature. Measurements were performed for Ga(+)(n) (n=17 39, and 40) over a 90-720 K temperature range. For Ga+39 and Ga+40 a broad maximum in the heat capacity-a signature of a melting transition for a small cluster-occurs at around 550 K. Thus small gallium clusters melt at substantially above the 302.9 K melting point of bulk gallium, in conflict with expectations that they will remain liquid to below 150 K. No melting transition is observed for Ga+17.

Human E4B, also called UFD2a, is a U-box-containing protein that functions as an E3 ubiquitin ligase and an E4 polyubiquitin chain elongation factor. E4B is thought to participate in the proteasomal degradation of misfolded or damaged proteins through association with chaperones. The U-box domain is an anchor site for E2 ubiquitin-conjugating enzymes but little is known of the binding mechanism. Using X-ray crystallography and NMR spectroscopy, we determined the structures of E4B U-box free and bound to UbcH5c and Ubc4 E2s. While previously characterized U-box domains are homodimeric, we show that E4B U-box is a monomer stabilized by a network of hydrogen bonds identified from scalar coupling measurements. These structural studies, complemented by calorimetry- and NMR-based binding assays, suggest an allosteric regulation of UbcH5c and Ubc4 by E4B U-Box and provide a molecular basis to understand how the ubiquitylation machinery involving E4B assembles.

Seasonal influenza virus causes significant morbidity and mortality each year. Point-of-care (POC) testing using rapid influenza diagnostic tests (RIDTs), immunoassays that detect viral antigens, are often used for diagnosis by physician offices and urgent care centers. These tests are rapid but lack sensitivity, which is estimated to be 50 to 70%. Testing by PCR is highly sensitive and specific, but historically these assays have been performed in centralized clinical laboratories necessitating specimen transport and increasing the time to result. Recently, Clinical Laboratory Improvement Amendments (CLIA)-waived, POC PCR influenza assays have been developed with >95% sensitivity and specificity compared to centralized PCR assays. To determine the clinical impact of a POC PCR test for influenza, we compared antimicrobial prescribing patterns of one urgent care location using the Cobas LIAT Influenza A/B assay (LIAT assay; Roche Diagnostics, Indianapolis, IN) to other urgent care centers in our health system using traditional RIDT, with negative specimens being reflexed to PCR. Antiviral prescribing was lower in patients with a negative LIAT PCR result (2.3%) than in patients with a negative RIDT result (25.3%; P < 0.005). Antivirals were prescribed more often in patients that tested positive by LIAT PCR (82.4%) than in those testing positive by either RIDT or reflex PCR (69.9%; P < 0.05). Antibacterial prescriptions for patients testing negative by LIAT PCR were higher (44.5%) than for those testing negative by RIDT (37.7%), although the difference was not statistically significant. In conclusion, having results from a PCR POC test during the clinic visit improved antiviral prescribing practices compared to having rapid results from an RIDT.

Calorimetry measurements, performed by multicollision induced dissociation, have been used to probe the melting of a number of (NaCl)nNa+ clusters with n=22-37. The clusters anneal at 225-325 K and melt at 750-850 K. (NaCl)22Na+ and (NaCl)37Na+, which can adopt geometries that are perfect fragments of the bulk lattice melt at around 850 K. The other clusters, which (except for n=31) must have defects, melt at temperatures which are up to 100 K lower than the perfect nanocrystals. The internal energy distributions become bimodal near the melting temperature. This is the signature of slow dynamic phase coexistence where clusters spontaneously jump back and forth between the solid and liquid states with an average period that is longer than required for thermal equilibration. The jump frequency must be between 10(4) and 10(7) s(-1) for the bimodal distribution to be observable in our experiments. The (NaCl)nNa+ clusters can dissociate by an unusual thermally activated process where melting and freezing raise the internal energy to generate hot solid clusters that can sublime before they cool to the ambient temperature.