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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 2650-2662 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The behaviors of polymer chains in simple shear flow and in flows with a large component of extension are now considered to be qualitatively different [R. B. Bird, C. F. Curtiss, R. C. Armstrong, and O. Hassager, Dynamics of Polymeric Liquids, 2nd ed. (Wiley, New York, 1987), Vol. 2, Chap. 13]. To examine the extensional case, we have fractured DNA molecules in solution in steady sink (primarily extensional) flow. DNA was chosen for this study because it can be obtained as monodisperse, unique-sequence material, and because the size distribution of the fracture fragments can be obtained by gel electrophoresis. Dilute monodisperse T7 DNA (Mw=26×106) solutions were recirculated through a 0.13 mm orifice in a flat plate. The flow field upstream of the orifice closely approximated an ideal sink flow, being free of vortices under the conditions used, DNA concentrations less than 12.5 μg/ml and flow rates less than 0.045 cm3/s. The kinetics of the fracture at low flow rates showed an initial lag period followed by a period of first-order rate; the lag period disappeared at higher flow rates while the first-order period persisted. The fracture rate increased exponentially with the flow rate. Contrary to the classic theory by Frenkel, our experimental results showed fracture products broadly distributed in size; this anomaly was explained by a bead-spring molecular-dynamics computer simulation. The simulation showed that just prior to chain fracture the chain was aligned parallel to the flow but contained many folds, so that points of maximum stress were not usually at the molecular center. These results suggest that the residence time in the converging flow was too short for the chain to reach complete extension.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 34 (1994), S. 1349-1358 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: DNA molecules ranging in size from 1 to 630 kilobase pair and intercalated with either ethidium bromide (EtBr) or propidium iodide (PI) were electrophoresed in 1% agarose at four different electric field strengths. The extent of intercalation of EtBr under the conditions of our electrophoresis experiments was determined by a spectroscopic technique, whereas the extent of intercalation of PI was inferred from previous studies. The effects of the increase in DNA contour length and the concomitant decrease of linear charge density were separated based on our analysis of the mobility data. We conclude that the main factor responsible for the reduced electrophoretic mobility of intercalated DNA is the diminished linear charge density and not the increased contour length. © 1994 John Wiley & Sons, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 39 (1996), S. 161-171 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Though the nearest neighbor exclusion model provides a good semiquantitative description of intercalation isotherms, it ignores the electrostatic interaction between cationic intercalators and DNA and underestimates binding in the neighborhood of θ = 0.5 intercalators per base pair.In order to improve the analysis and interpretation of intercalative binding curves, we (1) propose and develop a model that permits restricted but partial occupation of nearest neighbor sites, (2) discuss the advantages of using experimental variables for analysis rather than derived variables like θ/L for Scatchard plots, and (3) combine the lattice statistics of intercalation with the electrostatic free energy of intercalation as calculated by C. Bustamante and D. Stigter [(1984) Biopolymers, Vol. 23, pp. 629-645] to generate an isotherm that contains both effects.The analysis of data via the latter theory provides a description of the intercalation not only as a function of ligand concentration but also as a function of ionic strength and θ. The quantitative accuracy of the electrostatic theory can be checked by the standard ln K1 vs ln C plots. [M. T. Record, T. M. Lohman, and P. de Haseth (1976) Journal of Molecular Biology, Vol. 107, pp. 145-158], but appropriate data do not appear to be available at the present time. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 4
    Publication Date: 1990-02-15
    Print ISSN: 0021-9606
    Electronic ISSN: 1089-7690
    Topics: Chemistry and Pharmacology , Physics
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