Trophoblast L-selectin-mediated adhesion at the maternal-fetal interface

Trophoblast adhesion to the uterine wall is the requisite first step of implantation and, subsequently, placentation. At the maternal-fetal interface, we investigated the expression of selectin adhesion systems that enable leukocyte capture from the bloodstream. On the maternal side, human uterine epithelial cells up-regulated selectin oligosaccharide-based ligands during the window of receptivity. On the fetal side, human trophoblasts expressed L-selectin. This ligand-receptor system was functional, because beads coated with the selectin ligand 6-sulfo sLe(x) bound to trophoblasts, and trophoblasts bound to ligand-expressing uterine luminal epithelium in tissue sections. These results suggest that trophoblast L-selectin mediates interactions with the uterus and that this adhesion mechanism may be critical to establishing human pregnancy.     

Ordered liquid aluminum at the interface with sapphire

Understanding the nature of solid-liquid interfaces is important for many processes of technological interest, such as solidification, liquid-phase epitaxial growth, wetting, liquid-phase joining, crystal growth, and lubrication. Recent studies have reported on indirect evidence of density fluctuations at solid-liquid interfaces on the basis of x-ray scattering methods that have been complemented by atomistic simulations. We provide evidence for ordering of liquid atoms adjacent to an interface with a crystal, based on real-time high-temperature observations of alumina-aluminum solid-liquid interfaces at the atomic-length scale. In addition, crystal growth of alumina into liquid aluminum, facilitated by interfacial transport of oxygen from the microscope column, was observed in situ with the use of high-resolution transmission electron microscopy.     

Competitive hydration of quinazoline at the montmorillonite-water interface

Ultraviolet spectroscopic analyses of suspensions of quinazoline and Na(+)-saturated montmorillonite have indicated that covalent hydration of the monovalent organic cation is inhibited at or near the clay surface. A similar lack of hydration was observed in solutions of quinazoline and high-ionic-strength calcium chloride. The inhibition is attributed to a local competition between quinazoline and the inorganic cations for water of hydration.     

Deceleration of interstellar hydrogen at the heliospheric interface

High-resolution spectra of nearby stars show absorption lines due to material in the local interstellar cloud. This cloud is deduced to be moving at 26 kilometers per second with respect to the sun, and in the same direction as the "interstellar wind" flowing through the solar system. Measurements by the Ulysses spacecraft show that neutral helium is drifting through the solar system at the same velocity, but neutral hydrogen appears to be moving at only 20 kilometers per second, a result confirmed by new measurements of the hydrogen emission line taken by the High-Resolution Spectrograph on the Hubble Space Telescope. These results indicate that neutral hydrogen atoms from the local interstellar cloud are preferentially decelerated at the heliospheric interface, most likely by charge-exchange with interstellar protons, while neutral helium is unaffected by the plasma. The magnitude of the observed deceleration implies an interstellar plasma density of 0.06 to 0.10 per cubic centimeter, which in turn implies that the heliospheric shock should be less than 100 astronomical units from the sun.     

碳纤维木材复合材结合层剪切蠕变性能研究

为了研究碳纤维应用于建筑木构件及其节点加固工程中的长期承载性能,采用持续负载的剪切试验方法对碳纤维木材复合材结合层在高湿(温度60℃,相对湿度90％),低湿(温度24℃,相对温度45％)环境条件下的蠕变性能进行了研究.结论表明:Burger模型可较精确地模拟复合材结合层的短期剪切性能(R2≥98％);高湿环境下结合层剪切蠕变量显著大于低温环境,温度及相对湿度都是影响蠕变的重要因素;结合层厚度越大,剪切蠕变变形也越大,应力松弛较大,建议碳纤维与木材复合时施加一定的压力(0.05 MPa以上)以减少结合层厚度;高温环境下高应力水平的蠕变速率最大,较短时间便出现结合层断裂,在碳纤维设计应用时,应确保结合层剪切应力水平在极限应力的50％以内.图3参12     

Alkanes at the air-sea interface from offshore louisiana and Florida

Alkanes at the air-sea interface were analyzed in 118 surface samples collected at five different intervals over a 12-month period from Timbalier Bay (Louisiana), ogfshore Louiisiana, and offshore Florida. The alkanes were characterized by gas chromatography and mass spectrometry. Unexpectedly, methyl branched alkanes ranging in chain length froin C(15) to C(35) and cycloalkanes were frequently the predominant components. This suggests that the alkanes are produced by natural biological sources as well as human activities.     

Total alignment of calcite at acidic polydiacetylene films: cooperativity at the organic-inorganic interface

Biological matrices can direct the absolute alignment of inorganic crystals such as calcite. Cooperative effects at an organic-inorganic interface resulted in similar co-alignment of calcite at polymeric Langmuir-Schaefer films of 10,12-pentacosadiynoic acid (p-PDA). The films nucleated calcite at the (012) face, and the crystals were co-aligned with respect to the polymer's conjugated backbone. At the same time, the p-PDA alkyl side chains reorganized to optimize the stereochemical fit to the calcite structure, as visualized by changes in the optical spectrum of the polymer. These results indicate the kinds of interactions that may occur in biological systems where large arrays of crystals are co-aligned.     

Regulation of proteolysis at the neutrophil-substrate interface by secretory leukoprotease inhibitor

Human neutrophils can initiate the rapid degradation of extracellular matrix macromolecules by localizing the destructive process to sites of cell-substrate contact. Although plasma and its filtrates contain multiple proteinase inhibitors, these inhibitors did not prevent neutrophils from attacking either underlying fibronectin or elastin. However, subjacent substrates could be protected from neutrophils by recombinant secretory leukoprotease inhibitor, a structurally unique serine proteinase inhibitor whose natural counterpart is normally confined to human mucous secretions. The identification of this extravascular proteinase inhibitor as a potent regulator of subjacent proteolysis could lead to the development of a new class of anti-inflammatory therapeutics.     

Glucuronidase activation: enzyme action at an interface

Although the rate of hydrolysis by mammalian beta-glucuronidase appears to be inhibited by methylene chloride or carbon tetrachloride with the standard technique (phenolphthalein glucuronide as a substrate), the release of steroidal conjugates under conditions generally employed does not appear to be affected.     

Convergent solutions to binding at a protein-protein interface

The hinge region on the Fc fragment of human immunoglobulin G interacts with at least four different natural protein scaffolds that bind at a common site between the C(H2) and C(H3) domains. This "consensus" site was also dominant for binding of random peptides selected in vitro for high affinity (dissociation constant, about 25 nanomolar) by bacteriophage display. Thus, this site appears to be preferred owing to its intrinsic physiochemical properties, and not for biological function alone. A 2.7 angstrom crystal structure of a selected 13-amino acid peptide in complex with Fc demonstrated that the peptide adopts a compact structure radically different from that of the other Fc binding proteins. Nevertheless, the specific Fc binding interactions of the peptide strongly mimic those of the other proteins. Juxtaposition of the available Fc-complex crystal structures showed that the convergent binding surface is highly accessible, adaptive, and hydrophobic and contains relatively few sites for polar interactions. These are all properties that may promote cross-reactive binding, which is common to protein-protein interactions and especially hormone-receptor complexes.     

Enhanced protein adsorption at the solid-solution interface: dependence on surface charge

By the use of infrared internal reflection spectroelectrochemistry, it has been possible to observe an enhanced adsorption of porcine fibrinogen onto a germanium surface at potentials more positive than -200 millivolts relative to a saturated calomel electrode. The enhanced adsorption was observed directly at the interface between the solid and the aqueous solution.     

Free energy and temperature dependence of electron transfer at the metal-electrolyte interface

The rate constant of the electron-transfer reaction between a gold electrode and an electroactive ferrocene group has been measured at a structurally well-defined metal-electrolyte interface at temperatures from 1 degrees to 47 degrees C and reaction free energies from -1.0 to +0.8 electron volts (eV). The ferrocene group was positioned a fixed distance from the gold surface by the self-assembly of a mixed thiol monolayer of (eta(5)C(5)H(5))Fe(eta(5)C(5)H(4))CO(2)(CH(2))(16)SH and CH(3)(CH(2))(15)SH. Rate constants from 1 per second (s(-1)) to 2 x 10(4) s(-1) in 1 molar HClO(4) are reasonably fit with a reorganization energy of 0.85 eV and a prefactor for electron tunneling of 7 x 10(4) s(-1) eV(-1). Such self-assembled monolayers can be used to systematically probe the dependence of electron-transfer rates on distance, medium, and spacer structure, and to provide an empirical basis for the construction of interfacial devices such as sensors and transducers that utilize macroscopically directional electron-transfer reactions.     

Orbital reconstruction and covalent bonding at an oxide interface

Orbital reconstructions and covalent bonding must be considered as important factors in the rational design of oxide heterostructures with engineered physical properties. We have investigated the interface between high-temperature superconducting (Y,Ca)Ba(2)Cu3O7 and metallic La(0.67)Ca(0.33)MnO3 by resonant x-ray spectroscopy. A charge of about -0.2 electron is transferred from Mn to Cu ions across the interface and induces a major reconstruction of the orbital occupation and orbital symmetry in the interfacial CuO2 layers. In particular, the Cu d(3z(2)-r(2)) orbital, which is fully occupied and electronically inactive in the bulk, is partially occupied at the interface. Supported by exact-diagonalization calculations, these data indicate the formation of a strong chemical bond between Cu and Mn atoms across the interface. Orbital reconstructions and associated covalent bonding are thus important factors in determining the physical properties of oxide heterostructures.     

Adaptation of bulk constitutive equations to insoluble monolayer collapse at the air-water interface

A constitutive equation based on stress-strain models of bulk solids was adapted to relate the surface pressure, compression rate, and temperature of an insoluble monolayer of monodendrons during collapse at the air-water interface. A power law relation between compression rate and surface pressure and an Arrhenius temperature dependence of the steady-state creep rate were observed in data from compression rate and creep experiments in the collapse region. These relations were combined into a single constitutive equation to calculate the temperature dependence of the collapse pressure with a maximum error of 5 percent for temperatures ranging from 10 degrees to 25 degrees C.     

Reactions of solvated electrons initiated by sodium atom ionization at the vacuum-liquid interface

Solvated electrons are powerful reagents in the liquid phase that break chemical bonds and thereby create additional reactive species, including hydrogen atoms. We explored the distinct chemistry that ensues when electrons are liberated near the liquid surface rather than within the bulk. Specifically, we detected the products resulting from exposure of liquid glycerol to a beam of sodium atoms. The Na atoms ionized in the surface region, generating electrons that reacted with deuterated glycerol, C(3)D(5)(OD)(3), to produce D atoms, D(2), D(2)O, and glycerol fragments. Surprisingly, 43 ± 4% of the D atoms traversed the interfacial region and desorbed into vacuum before attacking C-D bonds to produce D(2).