Moduli of Quaternionic Superminimal Immersions of 2-Spheres into Quaternionic Projective Spaces

The aim of this paper is to describe the moduli spaces of degree d quaternionic superminimal maps from 2-spheres to quaternionic projective spaces HPn. We show that such moduli spaces have the structure of projectivized fibre products and are connected quasi-projective varieties of dimension 2nd + 2n + 2. This generalizes known results for spaces of harmonic 2-spheres in S⁴.     

Potassium ion mediated collagen microfibril assembly on mica

Potassium ion can critically effect the interaction between collagen microfibrils and mica leading to different ordered structures that vary dramatically with changing ion concentration. AFM images of the structures formed at different ion concentrations appear to be intermediate stages in the progression from disordered to ordered film. At 200 mM potassium ion concentration, a nanometer-thick array of aligned and bundled microfibrils covering large areas can be created easily and reproducibly on mica.     

Deprotecting thioacetyl-terminated terphenyldithiol for assembly on gallium arsenide

We characterize the assembly of terphenyldithiol (TPDT) on gallium arsenide (GaAs) from ethanol (EtOH) and tetrahydrofuran (THF) as a function of ammonium hydroxide (NH4OH) concentration. NH4OH facilitates the conversion of thioacetyl end groups of the TPDT precursor to thiolates in the assembly solution. The final structure of TPDT assembled on GaAs is sensitive not only to the assembly solvent but also to NH4OH concentration. In the presence of low concentrations of NH4OH (1 mM), TPDT assemblies from EtOH are oriented upright. The same assemblies are less upright when adsorption is carried out at higher NH4OH concentrations. In THF, TPDT does not adsorb significantly on GaAs at low NH4OH concentrations. The surface coverage and structural organization of these assemblies improve with increasing NH4OH concentrations, although these assemblies are never as organized as those from EtOH. The difference in the final structure of TPDT assemblies is attributed to differences in the thiolate fraction in the assembly solution at the point of substrate immersion.     

Theoretical transition probabilities for the OH Meinel system

The authors present a new potential energy curve, electric dipole moment function, and spin-orbit coupling function for OH in the X 2Pi state, based on high-level ab initio calculations. These properties, combined with a spectroscopically parametrized lambda-type doubling Hamiltonian, are used to compute the Einstein A coefficients and photoabsorption cross sections for the OH Meinel transitions. The authors investigate the effect of spin-orbit coupling on the lifetimes of rovibrationally excited states. Comparing their results with earlier ab initio calculations, they conclude that their dipole moment and potential energy curve give the best agreement with experimental data to date. The results are made available via EPAPS Document No. E-JCPSAG-017709.     

Nonlinear buckling analysis of hyperbolic cooling tower shell with ring-stiffeners

This paper is concerned with a numerical solution of hyperbolic cooling tower shell, a class of full nonlinear problems in solid mechanics of considerable interest in engineering applications. In this analysis, the post-buckling analysis of cooling tower shell with discrete fixed support and under the action of wind loads and dead load is studied. The influences of ring-stiffener on instability load are also discussed. In addition, a new solution procedure for nonlinear problems which is the combination of load increment iteration with modified R-C are- length method is suggested. Finally, some conclusions having important significance for practice engineering are given.The Project Supported by National Natural Science Foundation of China.     

A study of Src SH2 domain protein-phosphopeptide binding interactions by electrospray ionization mass spectrometry

The noncovalent binding of various peptide ligands to pp60^src (Src) SH2 (Src homology 2) domain protein (12.9 ku) has been used as a model system for development of electrospray ionization mass spectrometry (ESI-MS) as a tool to study noncovalently bound complexes. SH2 motifs in proteins are critical in the signal transduction pathways of the tyrosine kinase growth factor receptors and recognize phosphotyrosine-containing proteins and peptides. ESI-MS with a magnetic sector instrument and array detection has been used to detect the protein-peptide complex with low-picomole sensitivity. The relative abundances of the multiply charged ions for the complex formed between Src SH2 protein and several nonphosphorylated and phosphorylated peptides have been compared. The mass spectrometry data correlate well to the measured binding constants derived from solution-based methods, indicating that the mass spectrometry-based method can be used to assess the affinity of such interactions. Solution-phase equilibrium constants may be determined by measuring the amount of bound and unbound species as a function of concentration for construction of a Scatchard graph. ESI-MS of a solution containing Src SH2 with a mixture of phosphopeptides showed the expected protein-phosphopeptide complex as the dominant species in the mass spectrum, demonstrating the method’s potential for screening mixtures from peptide libraries.     

Increasing charge while preserving noncovalent protein complexes for ESI-MS

Increased multiple charging of native proteins and noncovalent protein complexes is observed in electrospray ionization (ESI) mass spectra obtained from nondenaturing protein solutions containing up to 1% (vol/vol) m-nitrobenzyl alcohol (m-NBA). The increases in charge ranged from 8% for the 690 kDa α₇β₇β₇α₇ 20S proteasome complex to 48% additional charge for the zinc-bound 29 kDa carbonic anhydrase-II protein. No dissociation of the noncovalently bound ligands/subunits was observed upon the addition of m-NBA. It is not clear if the enhanced charging is related to altered surface tension as proposed in the “supercharging” model of Iavarone and Williams (Iavarone, A. T.; Williams, E. R. J. Am. Chem. Soc. 2003, 125, 2319–2327). However, more highly charged noncovalent protein complexes have utility in relaxing slightly the mass-to-charge (m/z) requirements of the mass spectrometer for detection and will be effective for enhancing the efficiency for tandem mass spectrometry studies of protein complexes.     

Modulation of humoral immune response to oral BCG vaccination by Mycobacterium bovis BCG Moreau Rio de Janeiro (RDJ) in healthy adults

We hypothesize that the energy strategy of a cell is a key factor for determining how, or if, the immune system interacts with that cell. Cells have a limited number of metabolic states, in part, depending on the type of fuels the cell consumes. Cellular fuels include glucose (carbohydrates), lipids (fats), and proteins. We propose that the cell's ability to switch to, and efficiently use, fat for fuel confers immune privilege. Additionally, because uncoupling proteins are involved in the fat burning process and reportedly in protection from free radicals, we hypothesize that uncoupling proteins play an important role in immune privilege. Thus, changes in metabolism (caused by oxidative stresses, fuel availability, age, hormones, radiation, or drugs) will dictate and initiate changes in immune recognition and in the nature of the immune response. This has profound implications for controlling the symptoms of autoimmune diseases, for preventing graft rejection, and for targeting tumor cells for destruction.