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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 72-81 
    ISSN: 0886-1544
    Keywords: spectrin ; intrinsic fluorescence ; spectrin elasticity ; fluorescence quenching ; spectrin α chain ; spectrin β chain ; membrane skeleton ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: To better understand the solution structure of spectrin, the environments of its tryptophan residues have been examined by fluorescence spectroscopy. The spectra and the extent of quenching by several quenching agents have been determined for intact spectrin and its α and β subunits. The arsenal of quenchers used in the study represented both hydrophilic and hydrophobic species including anionic, cationic and neutral compounds. Effects on spectrin fluorescence of ethanol and ionic strength, which extend and/or rigidify spectrin, and of glycerol, which is commonly used in electron microscopy of the protein, have also been assessed in the presence and absence of quenchers. Most of the tryptophans of spectrin are either internally quenched or are sequestered, hindering the approach of hydrophilic quenching agents. Both the spectral shape and the extent of quenching by acrylamide indicate that some tryptophans of the β subunit are slightly more exposed in the isolated chain than in the dimer. Similar effects on spectra and on quenching of the intact dimer and of the isolated β chain are seen when the ionic strength is reduced. Ethanol and glycerol reduce spectrin tryptophan accessibility to 2-p-toluidinyl napthalene-6-sulfonic acid (TNS). It therefore appears that low ionic strength, α-β association and neutral solute (or lowered dielectric constant) all induce a similar, but modest conformational change in the domain structure. The extent of TNS binding is not increased by lowering the ionic strength, suggesting that the expansion and/or stiffening of the molecule in low electrolyte solutions does not involve exposure of significant numbers of hydrophobic sites. © 1994 Wiley-Liss, Inc.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 0947-6539
    Keywords: calixarenes ; lanthanides ; luminescence ; molecular dynamics ; N ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new family of cone-shaped podands and barrel-shaped cryptands based on calix[4]arenes incorporating 5,5′-substituted 2,2′-bipyridine subunits were prepared and characterized. The Eu3+ and Tb3+ complexes of the podands bearing two, three, or four bipyridine chromophores could be isolated. High molar absorption coefficients (εmax = 39 600M-1 cm-1 for Eu4 and 26 700M-1 cm-1 for Eu3) and high metal luminescence quantum yields (16% for Eu4 and 15% for Eu3) were obtained. Molecular dynamics simulations on Eu4 showed that the bipyridine arms wrap around the lanthanide cation, efficiently shielding the cation from solvent molecules. In the presence of chloride counter-ions the fourth bipyridine arms does not coordinate the lanthanide ion. Ligands bearing two bipyridine units and two additional functional groups - ethyl butyrate or N-propylpyrrole - did not give stable lanthanide complexes. The barre-land containing two calix[4]arene moieties and four bipyridine groups did not form complexes with lanthanide ions, most probably because of the rigidity of the ligand.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 165 (1995), S. 588-599 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Upon binding to their receptors on the surface of neutrophils, chemotactic peptides elicit a burst of metabolic activity. The excess acid generated by this burst must be rapidly extruded in order to maintain intracellular pH and preserve normal microbicidal responses. Recently, H+-pumping vacuolar-type ATPases (V-pumps) and a H+-selective conductance were described in the membrane of neutrophils. However, these systems are virtually quiescent in resting cells. In this report, we analyzed whether the V-pumps and the conductance become active and contribute to pH regulation following cell activation by chemoattractants. Formyl-Met-Leu-Phe (fMLP) was found to stimulate V-pumps, as assessed by the appearance of bafilomycin-sensitive H+ extrusion. Concomitantly, the chemoattractant also activated the H+ conductance, detected as a voltage-dependent and Zn2+-sensitive net H+ efflux. In both cases, activation was prevented by treatment with competing antagonistic peptides or with pertussis toxin, implying mediation by a receptor copuled to a heterotrimeric G protein. The signalling pathways downstream of the G proteins were also investigated. Stimulation of neither th V-pump nor the conductace required activation of protein kinase C. An elevation of cytosolic calcium ([Ca2+]i) comparable to that induced by fMLP did not suffice to trigger either transporter. Moreover activation of the conductance remained unaffected when the chemoattractant-induced increase in [Ca2+]i was precluded. In contrast, stimulation of the V-pump was substantially (∞50%) depressed when [Ca2+]i was prevented from rising. Tyrosine phosphorylation of several polypeptides accompanies stimulation by fMLP. Prevention of phosphotyrosine accumulation resulted in a pronounced inhibition of H+-pumping and of the H+ conductance. Together, these data indicate that engagement of surface receptors by chemotactic peptides can lead to stimulation of two voltage-sensitive pH regulatory pathways, a pump and a conductance, by a pathway that requires tyrosine phosphorylation. Both pathways are capable of sizable H+ extrusion, thereby contributing to pH regulation during the metabolic burst. © 1995 Wiley-Liss Inc.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 12 (1977), S. 215-223 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The invariance question int he CNDO and INDO levels of approximation is discussed with particular reference to one-center and two-center two-electron integrals and rotation of molecule-fixed coordinate axes. It is shown that asufficient condition for rotational invariance for the cone-center two-electron integrals is Jμμ = Jμμ, +2Kμμ, where J and K are the Coulomb and exchange integrals over orbitals μ μ′ with the same azimuthal quantum number. CNDO and INDO procedures, which explicitly employ Löwdin's orthogonalized basis set of atomic ortbitals (OAO) and differentiate between s-, p-, and d-orbitals on an atom in calculating various integrals, have also been examined in relation to the rotational invariance requirement. An expression which satisfies rotational invariance for two-electron Coulomb repulsion integrals over OAOS is also given.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 6 (1972), S. 819-841 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The spin density distribution in a few hydrocarbon radicals has been calculated using orthogonalized atomic orbitals in the Unrestricted Hartree-Fock formalism of Amos and Snyder and including certain more important two-electron hybrid and exchange integrals and all the core-resonance integrals. Our calculated spin densities for the cation and anion radicals of alternant hydrocarbons, which are now different due to the breakdown of the pairing theorem, are, in general, of the right relative order so that even the simple McConnell type of relation can account partly for the observed differences in the proton splittings between cations and anions. The proton splittings for position 2 of naphthalene and anthracene radical ions are correctly predicted, thus clearing up the well-known cation-anion anomaly for this position. Comparative calculations have been made to show that the spin density results are worsened with the neglect of the integrals of the type mentioned before. An empirical analysis correlating the observed 13C splittings and the spin density results over a non-orthogonal basis set shows that the available 13C splittings in alternant hydrocarbon radical ions can be explained with a set of sigma-pi parameters which are consistent with the theory. It is shown that even though the spin densities in cations and anions may be different, these can lead to similar 13C splittings.
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  • 6
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A modified INDO procedure has been used to calculate the proton hyperfine splittings in benzyl and the isoelectronic anilino, phenoxy and 2-azabenzyl as well as 2- and 3-thenyl radicals. The present procedure differentiates between s-, p- and d-orbitals on an atom in estimating various integrals involving them, satisfies the rotational invariance requirements and employs an orthogonalized basis set of atomic orbitals for obtaining core-Hamiltonian matrix elements. The calculations based on using the exponents which depend only on the type of orbital and the nature of atom fail to provide correct relative order of ortho and para proton splittings in benzyl as well as anilino, phenoxy and 2-azabenzyl radicals. On the other hand, use of the exponents which are modified according to the charge densities in various orbitals leads to a high absolute value for para proton splitting compared to that for ortho proton splitting which in case of all these radicals is in agreement with experiment. A spin density calculation on benzyl, anilino and phenoxy radicals considering the variation of one-center one-electron and one-center two-electron integrals for different protons with their charges is found to yield further improvement in the relative order of ortho and para proton splittings in all these radicals. In 2- and 3-thenyl radicals the role of 3d-orbitals on sulfur has also been examined. To our knowledge, no unrestricted INDO calculations including 3d-orbitals on sulfur have been reported in the literature so far.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 591-599 
    ISSN: 0268-2605
    Keywords: arsenic speciation ; LC-ICP-MS ; validation ; urine samples ; background levels ; The Netherlands ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The method validation for the speciation of five arsenic species in urine samples by liquid chromatography hyphenated to inductively coupled plasma mass spectrometry is described. Arsenic species which are identified and quantified in urine samples are the anions of arsenic(III), arsenic(V), monomethylarsonic acid and dimethylarsinic acid, and the cationic arsenobetaine. Detection limits were obtained in the range 0.3-0.4 μg As l-1 while the repeatability was in the range 3-4% (RSD) for concentrations above five times the detection limit. Urine samples could be analysed directly after a ten-fold dilution step. Arsenic compound concentrations were determined in urine samples from a volunteer who consumed a portion of tuna fish high in arsenobetaine. It was found that arsenobetaine was excreted rapidly via the urine with maximum concentrations after 12 h. Nearly complete arsenobetaine excretion was reached after 48 h. Background levels of arsenic compounds were determined in 61 urine samples from non-exposed inhabitants of The Netherlands. © 1998 John Wiley & Sons, Ltd.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 879-893 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinylsulfonylethyl (VSE) derivatives of the nucleic acid bases adenine, thymine, cytosine, and the nucleosides inosine and uridine have been prepared via a simple Michael reaction with divinyl sulfone. The VSE derivatives were grafted on a polyethyleneimine (PEI) backbone. PEI of different molecular weights (1400, 1800 and 50,000-100,000) were used and also two different molar ratios (1:1 and 1:2) of monomer to PEI were employed. From the 1H-NMR and elemental analysis, it appeared that in almost all instances the grafting was quantitative. In one case, both 1-VSE-thymine and 9-VSE-adenine were grafted on the same PEI backbone. Interactions between some of these polymers were investigated by UV spectroscopy. The expected complementary base pairing was observed only in DMSO-ethylene glycol solvent system but not in DMSO. The adenine polymer showed a one-to-one interaction with the thymine polymer.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 2545-2554 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sulfonated phenol formaldehyde resins were prepared under different conditions. Composites of these resins with sulfonated coals were also prepared and their physical properties and structure were studied. It was found that the resins are macroreticular and possess high surface areas.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 813-820 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly-6-(acryloyloxymethyl)uracil was prepared by radical-catalyzed polymerization of monomeric 6-(acryloyloxymethyl)uracil. The reaction of 6-chloromethyluracil with the potassium salt of polyacrylic acids of molecular weights 5000 and 90,000 gave polymers with both carboxylate groups and 50-70% pendant uraciles. Some inferences concerning the arrangement of uracil groups are drawn from the nuclear magnetic resonance (NMR) spectra of the latter polymers. No interaction between poly(A) and the synthetic polymers could be observed.
    Additional Material: 3 Ill.
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