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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 13 (1974), S. 1821-1845 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laser Raman spectra of the trinucleoside diphoshate ApApA and dinucleoside phosphates ApU, UpA, GpC, CpG, and GpU are reported and discussed. Assignments of conformationally sensitive frequencies are-facilitated by comparison with spectra reported here of poly(rA), poly(rC), and poly(rU) in deuterium oxide solutions. The significant spectral differences between ApU and UpA, and between GpC and CpG, reveal that the sequence isomers have nonidentical conformations in aqueous solution. In UpA at low temperature the bases are stacked and the backbone conformation is similar to that found in ordered polynucleotide structures and RNA. In ApU no base stacking can be detected and the backbone conformation differs from that found in UpA, both in the orientation of phosphodiester linkages and in the internal conformation of ribose. At the conditions employed neither ApU nor UpA exhibits base pairing in aqueous solutions. In both GpC and CpG the bases are stacked and the phosphodiester conformations are similar to those encountered for UpA and RNA. However, major differences between spectra of GpC and CpG indicate that the geometries of stacking and ribosyl conformations are different. In GpC the Raman data favor the formation of hydrogen bonded dimers containing GC pairs. Protonation of C in GpC is sufficient to eliminate the ordered conformation detected by Raman spectroscopy. Despite the ordered backbone conformation evident in GpU, this dinucleoside apparently contains neither stacked nor hydrogen bonded bases at the conditions employed here. The Raman data also confirm the stacking interactions in ApApA, poly(rA), and poly(rC) but suggest that the backbone conformation in poly(rC) differs qualitatively from that found in most ordered polynucleotide structures and is thermally more stable. The present results demonstrate the sensitivity of the Raman technique to sequence-related structural differences in oligonucleotides and provide additional spectra-structure correlations for future conformational studies of RNA by laser Raman spectroscopy.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 11 (1972), S. 2423-2437 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laser-excited Raman spectra of the double-helical complexes poly A·poly U and poly G·poly C are reported for 2H2O and H2O solutions. The spectra are discussed in relation to their use as quantitative reference spectra for determining the dependence of the Raman scattering of RNA on secondary structure. The Raman line at 815 cm-1, due to the phosphodiester group, exhibits the same intrinsic intensity in spectra of poly A·poly U and poly G·poly C and is thus dependent only upon the amount of ordering of the helix and not on the kinds of nucleotides involved. The hypochromic Raman lines in spectra of poly A·poly U are identified and their intensity changes are determined quantitatively over the temperature range 32-85°C. Comparison of the spectra in the 1500-1750 cm-1 region reveals that the Raman lines from carbonyl group vibrations of uracil are about sevenfold more intense than those of guanine and cytosine for both paired and unpaired states and will thus dominate the spectra of RNA. The Raman frequencies in this region are also compared with previously reported infrared frequencies and give evidence of being strongly perturbed by base-stacking interactions in the helices.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 765-789 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Raman spectra of polyribocytidylic acid show the formation of an ordered single-stranded structure [poly(rC)] at neutral pH and an ordered double-stranded structure containing hemiprotonated bases [poly(rC)·poly(rC+)] in the range 5.5 〉 pH 〉 3.7. Below 40°C, poly(rC) contains stacked bases and a backbone geometry of the A-type, both of which are gradually eliminated by increasing the temperature to 90°C. Below 80°C, poly(rC)·poly(rC+) contains bases which are hydrogen bonded and stacked and a backbone geometry also of the A-type. In this structure the bases of each strand are shown to be structurally identical, i.e., hemiprotonated, and therefore distinct from both neutral and protonated cytosines. Infrared and Raman spectra indicate the existence of a center of symmetry with respect to the paired cytosine residues, which suggests that the additional proton per base pair is shared equally by the two hydrogen-bonded bases. Denaturation of poly(rC)·poly(rC+) occurs cooperatively (tm ≈ 80°C) with elimination of base stacking, base pairing, and the A-helix geometry. Each of the separated strands of the denatured complex is shown to contain comparable amounts of both neutral and protonated cytosines, most likely in alternating sequence [poly(rC, rC+)]. In both poly(rC, rC+) and poly(rC), at 90°C, the backbones do not exhibit the phosphodiester Raman frequencies characteristic of other disordered polyribonucleotide chains. This is interpreted to mean that the single strands, though devoid of base stacking and A-type structure, contain uniformly ordered backbones of a specific type. Fully protonated poly(rC+), on the other hand, forms no ordered structure and may be characterized as a disordered (random chain) polynucleotide at all temperatures. Several Raman lines of poly(rC) are absent from the spectrum of poly(rC)·poly(rC+) and vice versa. These frequencies, assigned mainly to vibrations of the ribose groups, suggest that the furanose ring conformations are different in the single-stranded and double-stranded structures of polyribocytidylic acid. Several other Raman group frequencies have been identified and correlated with the polymer secondary structures.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oriented fibers drawn from aqueous gels of calf-thymus DNA were maintained at constant relative humidites of 75 and 92% to yield canonical A-DNA and B-DNA structures, respectively. Raman spectra of the two forms of DNA were recorded over the spectral range 300-4000 cm-1. The authenticated DNA fibers were deuterated in hygrostatic cells containing D2O at appropriate relative humidities, and the corresponding spectra of deuterated DNAs were also obtained. The spectra reveal all of the Raman scattering frequencies and intensities characteristic of A- and B-DNA structures in both nondeuterated and deuterated froms, as well as the frequencies and intensities of adsorbed solvent molecules from which the hydration content of DNA fibers can be calculated. Numerous conformation-sensitive vibrational modes of DNA bases and phosphate groups have been identified throughout the 300-1700-cm-1 interval. Evidence has also been obtained for conformation sensitivity of deoxyribosyl CH stretching modes in the 2800-3000-cm-1 region. Raman lines of both the backbone and the bases are proposed as convenient indicators of A- and B-DNA structures. The results are extended to Z-DNA models investigated previously. Some implications of these findings for the determination of DNA or RNA structure from Raman spectra of nucleoproteins and viruses are considered.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 26 (1987), S. 934-936 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Laser-excited Raman spectra of tRNAPhe from yeast and of fractionated 16S and 23S rRNA from E. coli are reported for samples in aqueous solution and in the solid state. The Raman scattering spectrum of each RNA is not significantly altered by the change from an aqueous to a solid environment and displays the same characteristic frequencies and intensities associated with ordered polyribonucleotide structures. Unlike DNA, the backbone conformation of RNA thus appears to be largely insensitive to gross changes in the degree of hydration.Raman scattering from the phosphate group vibrations of aqueous tRNAyeastPhe is qualitatively and quantitatively the same as obtained from previously studied tRNA's and is indicative of a highly ordered conformational structure in which some 85% of the nucleotide residues are in ordered configurations. The major differences observed between spectra of tRNA and rRNA are attributed to differences in base composition of these RNA's.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 1 (1973), S. 207-215 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Raman spectra of poly(rG), obtained from neutral aqueous solutions containing excess sodium counterions, are qualitatively different than spectra obtained from salt-free solutions. In the presence of a two-fold molar excess of Na+ (per phosphate group) the Raman spectrum of poly(iG) closely resembles that of the gel of Guo-5′-P and is characteristic of an ordered helical structure in which guanine residues are hydrogen bonded to one another. In the absence of added salt the spectrum of poly(rG) is characterized by unusual guanine ring frequencies which suggests a tautomeric or ionic modification of the ordinary (keto-amino) ring structure. Both the high-salt and no-salt forms of poly(rG) represent stable secondary structures as evidenced by the conformationally sensitive phosphodiester frequencies and by the absence of significant spectral changes on heating the solutions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 9 (1980), S. 134-136 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Rates of deuterium exchange of the 8-CH groups of 5′-rGMP and cGMP in D2O solutions (KH) are compared with rates of protium exchange of the 8-CD groups of the same compounds in H2O solutions (KD). The ratio of the two rate constants (kH/kD) defines an isotope effect which is a combination of primary kinetic and solvent isotope effects, the former predominating. The net isotope effect was measured by Raman spectrophotometry over the temperature range 30-80°C. The Arrhenius activation energies (Ea) and pre-exponential frequency factors (A) were also determined. The average values of kH/kD are 1.82 ± 0.15 for 5′-rGMP and 1.43 ± 0.06 for cGMP. The relatively small kinetic isotope effects are indicative typically of an unsymmetrical transition state. The ratio EaH/EaD is unity in both compounds, indicating an early or reactant-like transition state. The present data are consistent with, and extend the range of, the Bell-Goodall curve relating log (kH/kD) to ΔpK of the two acid-base systems involved in the proton transfer during the rate-determining step.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates (kH) of deuterium exchange of 8-CH groups, as well as the rates (kD) of protium exchange of 8-CD groups in 5′-IMP and cIMP, were measured by laser Raman spectrophotometry over the temperature range 30-80°C. The kH, or ‘forward’ rates, were determined from exchange in D2O solutions, while the kD, or ‘reverse’ rates, were determined from exchange in H2O solutions of the nucleotides. The hypoxanthine nucleotides were found to exchange with rates intermediate between those of corresponding adenine and guanine nucleotides, reported previously. The values obtained for the rate constants as a function of temperature (k=A exp (-Ea/RT)) yield the following Arrhenius activation energies and frequency factors. For 5′-IMP: EaH=25.5±0.6 kcal mol-1, AH=2.61×1015h-1; EaD=24.9±0.6 kcal mol-1, AD=4.32×1014h-1. For cIMP: EaH=22.2±0.6 kcal mol-1, AH=2.52×1013h-1; EaD=21.4±0.6 kcal mol-1, AD=3.93×1012h-1. The lower activation energy for cIMP accounts for its more rapid exchange vis-à-vis 5′-IMP, confirming the trend observed also for adenine and guanine nucleotides. Moreover, as in the cases of adenine and guanine isomers, the differential exchange between cyclic and 5′-nucleotides of hypoxanthine is large at lower temperatures and small at higher temperatures. These results confirm that exchange at 8-C is influenced by the ribosyl phosphate group. The present data also provide evidence of small kinetic isotope effects in the 8-C exchange reactions. For 5′-IMP, kH/kD≈2.5, and for cIMP, kH/kD≈1.7. The isotope effects of 5′-IMP and cIMP are close to the values observed for guanine nucleotides. Finally, Raman vibrational spectra of four isotopic modifications of the hypoxanthine nucleotides are compared to provide specific assignments of the Raman bands to vibrations of the purine skeleton and its exocyclic substituents.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Each of the hypoxauthine residues of the dinucleoside monophosphate, inosylyl(3′→5′)inosine (IpI), manifests the same rate of deuterium exchange of the proton at the 8-C ring position, as measured by Raman spectrophotometry. In the temperature interval 30-80°C and at neutral pD, the exchange rate constants yield Arrhenius parameters (Ea = 22.4±0.6 kcal mol-1; A = 2.13 × 1013 h-1) that are identical to values obtained on inosine-3′:5′-monophosphate (cIMP), but different from those of inosine-5′-monophosphate (5′-IMP) which exchanges more slowly. The results confirm that nucleotides containing the monovalent phosphate anion, exchange more rapidly than those containing the divalent phosphate anion, and suggest further that base stacking in IpI does not greatly retard the speed of 8-CH exchange of either of the hypoxanthine rings.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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