Cellular depletion of p56lck during thymocyte apoptosis

The src-related protein tyrosine kinase p56lck is thought to be important in regulating maturation and functional responsiveness of T cells and thymocytes. In the present studies we report that expression of p56lck is suppressed during apoptosis. Using primary cultures of rat thymocytes, we found that agents that are effective in inducing apoptosis, including okadaic acid, dexamethasone, and antibodies to the CD3 receptor, also deplete cells of p56lck. This process is rapid, occurring within 24 h, and is not due to cytotoxicity. Inhibition of DNA fragmentation in apoptotic cells with the endonuclease inhibitor ZnCl2 failed to prevent depletion of p56lck, suggesting that it was not a consequence of the DNA degradation process. Using the thymic lymphoma cell line LSTRA, apoptosis was also associated with cellular depletion of p56lck. In contrast to thymocytes, this process required 48-72 h possibly because these cells overexpress p56lck. Although at this time we are uncertain as to the precise role of p56lck in the process of apoptosis, our results indicate that changes in the expression of this protein in thymocytes is an important marker of programmed cell death.     

Diffusive self-ignition of hydrogen upon efflux from a nozzle array

It is experimentally demonstrated that the efflux of hydrogen at a high pressure into air via a nozzle array is accompanied by the interaction of jets, which results in the conditions for self-ignition at a nozzle diameter below the values for which self-ignition is possible in a single jet. Conditions for the safe efflux of hydrogen via a nozzle array from a reservoir at a pressure of 400 bar (and below) are established.     

Impact of Particle Generation Method on the Apparent Hygroscopicity of Insoluble Mineral Particles

Calcite (CaCO ₃ ) mineral particles are commonly generated by atomization techniques to study their heterogeneous chemistry, hygroscopicity, and cloud nucleation properties. Here we investigate the significant artifact introduced in generating calcium mineral particles through the atomization of a saturated suspension of the powder in water, by measuring particle hygroscopicity via CCN activation curves. Particles produced from atomization displayed hygroscopicities as large as κ_app > 0.1, 100 times more hygroscopic than that obtained for dry-generated calcite, κ_app = 0.0011. The hygroscopicity of the wet-generated particles increased as a function of time the calcite powder spent in water, and with decreasing particle size. Wet-generated calcium oxalate was more hygroscopic through wet- (κ_app = 0.34) versus dry-generation (κ_app = 0.048). Atomized calcium sulfate particles, however, were only slightly more hygroscopic (κ_app = 0.0045) than those generated dry (κ_app = 0.0016). Single-particle analysis by ATOFMS and SEM/EDX, and bulk analysis of the calcite powders by ICP-MS and IC revealed no significant soluble contaminants. The atomized particles were likely composed of components that dissolved from the powder and then re-precipitated, and appeared to contain little of the original mineral powder. The increased hygroscopicity of atomized calcite may have been caused by aqueous carbonate chemistry producing Ca(OH) ₂ , Ca(HCO ₃ ) ₂ , and metastable hydrates with increased solubility. Surface water adsorption may have also played a role, in addition to uncharacterized soluble components produced by wet-generation, and the precipitation of amorphous phases including glassy states. This study suggests that using wet-generation methods to suspend mineral dust samples will not produce particles with the correct physicochemical properties in laboratory studies, a finding which has important implications for past and future laboratory studies focusing on understanding relationships between the hygroscopicity and chemistry of mineral dust particles.     

Ultrasound screening for deep venous thrombosis after total knee arthroplasty. 2-year reassessment

The efficacy of ultrasound compared with ascending venography for the detection of deep venous thrombosis immediately after total knee arthroplasty was assessed after a 2-year interval. One hundred thirty-seven patients were eligible for the study; however, 31 patients received only one of the screening methods and a color Doppler examination was inconclusive in six patients. Therefore, 100 patients had a Doppler examination and a venogram. Overall, the sensitivity of ultrasound was 85%, the specificity 97%, the positive predictive value 85%, the negative predictive value 97%, and the accuracy 95%. The sensitivity in the calf was 83%, in the popliteal vein 86%, and in the femoral vein 100%. Two years ago, the initial assessment of ultrasound for the detection of deep venous thrombosis after surgery in patients who had total joint arthroplasty revealed a 75% sensitivity, 99% specificity, 91% positive predictive value, 97% negative predictive value, and 97% accuracy. The sensitivity in the calf was 83%; the sensitivity in the popliteal vein was 40%; and the sensitivity in the femoral vein was 50%. After 2 years of using this screening test with one technician and one radiologist, an improvement with this noninvasive technique was shown. However, it was found that Doppler imaging is not as sensitive as venography for detecting calf thrombi. Any imaging technique should be validated by each institution to determine the validity of the instrument and the learning curve of the technician administering the examination.     

Charge-remote fragmentation of odd-electron peptide ions

Comparison between the gas-phase fragmentation of odd-electron M+*, [M + H]2+*, and [M - 2H]-* ions of model peptides suggests that charge-remote radical-driven fragmentation pathways play an important role in the dissociation of odd-electron peptide ions. We have found that charge-remote processes are responsible for a variety of side-chain losses from the precursor ion and some backbone fragmentation. These fragmentation pathways most likely involve hydrogen abstraction by the radical site that initiates subsequent cleavages. These findings are generally relevant to our understanding of the fragmentation patterns of odd-electron peptide ions produced through various approaches including the capture of low-energy electrons, electron detachment, and electron transfer.     

Tissue imaging using nanospray desorption electrospray ionization mass spectrometry

Ambient ionization imaging mass spectrometry is uniquely suited for detailed spatially resolved chemical characterization of biological samples in their native environment. However, the spatial resolution attainable using existing approaches is limited by the ion transfer efficiency from the ionization region into the mass spectrometer. Here, we present a first study of ambient imaging of biological samples using nanospray desorption ionization (nano-DESI). Nano-DESI is a new ambient pressure ionization technique that uses minute amounts of solvent confined between two capillaries comprising the nano-DESI probe and the solid analyte for controlled desorption of molecules present on the substrate followed by ionization through self-aspirating nanospray. We demonstrate highly sensitive spatially resolved analysis of tissue samples without sample preparation. Our first proof-of-principle experiments indicate the potential of nano-DESI for ambient imaging with a spatial resolution of better than 12 μm. The significant improvement of the spatial resolution offered by nano-DESI imaging combined with high detection efficiency will enable new imaging mass spectrometry applications in clinical diagnostics, drug discovery, molecular biology, and biochemistry.     

Applications of high-resolution electrospray ionization mass spectrometry to measurements of average oxygen to carbon ratios in secondary organic aerosols

The applicability of high-resolution electrospray ionization mass spectrometry (HR ESI-MS) to measurements of the average oxygen to carbon ratio (O/C) in secondary organic aerosols (SOAs) was investigated. Solutions with known average O/C containing up to 10 standard compounds representative of low-molecular-weight SOA constituents were analyzed and the corresponding electrospray ionization efficiencies were quantified. The assumption of equal ionization efficiency commonly used in estimating O/C ratios of SOAs was found to be reasonably accurate. We found that the accuracy of the measured O/C ratios increases by averaging the values obtained from both the posive and negative modes. A correlation was found between the ratio of the ionization efficiencies in the positive (+) and negative (-) ESI modes and the octanol-water partition constant and, more importantly, the compound's O/C. To demonstrate the utility of this correlation for estimating average O/C values of unknown mixtures, we analyzed the ESI (+) and ESI (-) data for SOAs produced by oxidation of limonene and isoprene and compared them online to O/C measurements using an aerosol mass spectrometer (AMS). This work demonstrates that the accuracy of the HR ESI-MS method is comparable to that of the AMS with the added benefit of molecular identification of the aerosol constituents.