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  • 1
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 106 (1984), S. 8079-8086 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 97 (1975), S. 6624-6628 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 367 (1981), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-0689
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Theoretical calculations using a two-state model of counterion phosphate interactions have been performed in order to determine the electrostatic stability of DNA in various ionic environments. Comparison of the stabilities of different conformations leads to results consistent with the B→Z transitions observed in high-salt environments and suggest that at very low ionic strnegths the left-handed Z(II) form is an electrostatically preferred conformation. An ion-type dependence of the high-salt B→Z transition midpoint is predicted. Calculations of the energies of the A and C conformations are also discussed in relation to experimentally observed transitions.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 38 (1990), S. 133-143 
    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: Molecular mechanics calculations have been used to study the external noncovalent complexes formed between DNA and the strong carcinogen, aflatoxin B1. Three different sequences of hexameric duplexes were used for the DNA. Both the aflatoxin B1 parent molecule and its ultimate carcinogenic form, a carbocation, were modeled. The results are compared with recent experimental data on sequence specificity of the covalent attachment of aflatoxin to sites on the nucleotide bases. The comparison is discussed in light of a recently proposed hypothesis suggesting that the locus of carbocation formation is in acidic domains near the surface of the macroion and this determines the site of covalent adduct formation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 44 (1992), S. 1-14 
    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: Kinetic studies of the hydrolysis of benzo[a]pyrene diol epoxides have shown that hydrolysis proceeds through an acid-catalyzed SN1 mechanism and that the rate-determining step is the formation of a benzylic carbocation. The formation of this carbocation indicates that the diol epoxide can react with nucleophilic sites on DNA as an alkylating agent. Previous work has indicated that the kinetic data could be accurately fit to kobsd = kH [H+] + k0, in which kH [H+] is the pseudo first-order rate constant for acid-catalyzed hydrolysis and k0 is the rate constant for spontaneous hydrolysis. The observation made in several laboratories, that DNA catalyzes the hydrolysis of carcinogenic diol epoxides, is of direct interest in light of our recent calculation indicating that the local environment of DNA has a high concentration of hydrogen ions. The significance of acidic domains around nucleic acids is primarily in the ability of the protons to catalyze reactions. We have hypothesized that the high concentration of hydrogen ions at the DNA surface is responsible for the catalysis and that the generation of benzylic carbocations at the DNA surface can result in either nontoxic tetraols or in mutagenic nucleotide adducts, depending on the nucleophile with which the carbocation reacts. The calculations presented here are concerned with qualitatively understanding the rate constants in terms of the mechanisms of the acid-catalyzed and the spontaneous (H2O-catalyzed) hydrolyses. © 1992 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 48 (1993), S. 213-230 
    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: Metropolis Monte Carlo and Poisson-Boltzmann calculations were done to quantitatively assess the conditions under which counterion condensation (CC) theory could be considered valid. The fundamental prediction of condensation theory, that the number of counterions bound to a polyelectrolyte molecule can be predicted by a single parameter describing the linear charge density of the charged system, was shown to be quantitatively correct for a range of conditions. To define the number of counterions bound, it was necessary to use an energy-based criterion by which ions that interact with the polyion with an energy less than -kT were considered bound. Using this criterion, Monte Carlo calculations on systems consisting of charged cylinders and a neutralizing number of counterions in a dielectric continuum showed that the number of bound counterions was quantitatively predictable by the CC relation (1-1/ξ) for systems with a linear charge density and dimensions approaching those of duplex or triplex DNA. Poisson-Boltzmann (PB) calculations on cylinders with different linear charge densities and radii have been done to assess the limits of the CC prediction that the number of counterions bound is a constant even as the bulk concentration of electrolyte in the surrounding is increased. As in the case of the MC calculations, the validity of the CC prediction is seen to increase with increasing linear charge density of the charged cylinder. The agreement between PB and CC is seen to be very good for highly charged cylinders. The results described here provide justification for the use of CC theory for interpreting experimental data on polyelectrolytes of the approximate dimensions and linear charge density of duplex or triplex DNA. © 1993 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 56 (1995), S. 29-37 
    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 aziridine analogues of the epoxide metabolites of carcinogenic polycyclic aromatic hydrocarbons have greater mutagenic potency than the epoxides. Like their well-studied analogues, the aziridines undergo a pH-dependent decomposition that leads to a reactive carbocation intermediate. In aqueous solution the nucleophile with which the carbocation generally reacts is water. The kinetics of this pH-dependent reaction have been experimentally characterized by others. Although the effect of DNA on this reaction has not been studied, we hypothesize that, like their epoxide analogues, the aziridine derivatives of polycyclic aromatic hydrocarbons undergo a DNA-catalyzed reaction leading through a carbocation to either a DNA-adduct or a hydrolysis product. Using Poisson-Boltzmann calculations in conjunction with Metropolis Monte Carlo simulations and energy-minimized conformations, we predict the DNA-dependence of the acidcatalyzed decomposition of the K-region aziridine, phenanthrene[9,10]imine. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 65 (1997), S. 1087-1093 
    ISSN: 0020-7608
    Keywords: Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recent work by the authors on the calculation of local solvent dielectric constants around polyelectrolytes using the Poisson-Boltzmann approach is analyzed in terms of the effect on surface potentials and counterion concentrations. Polyelectrolyte surface geometry, local electric fields, and counterion distributions contribute to the self-consistent prediction of local solvent dielectric constants. For an all-atom cell model of DNA with added monovalent salt varying from 0 to 0.5M, the Poisson-Boltzmann-determined electrostatic potential increases (negatively) by 50-100% upon the inclusion of local dielectric constants. This, in turn, implies that hydronium ion concentrations in the major and minor grooves increase by about 0.65 and 0.35 pH units, respectively. While counterion concentrations in the major groove change only slightly, those in the minor groove increase by 60-90%. It is also noted that while the local dielectric constant in the major groove monotonically increases away from the surface toward the bulk value of water the dielectric constant in the minor groove has a minimum about 2 Å from the surface due primarily to the local electric field. Certain other properties, such as ionic and dipole first passage times, are affected little by local dielectric constants (less than about 3%).   © 1997 John Wiley & Sons, Inc. Int J Quant Chem 65: 1087-1093, 1997
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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