An Investigation of the Dynamics of Spermine Bound to Duplex and Quadruplex DNA by (13)C NMR Spectroscopy. a Keniry, M. & a Owen, E. European biophysics journal : EBJ, 36(6):637–46, July, 2007. doi abstract bibtex A detailed analysis of the (13)C relaxation of (13)C-labelled spermine bound to duplex and quadruplex DNA is presented. T(1), T(2) and heteronuclear NOE data were collected at four (13)C frequencies (75.4, 125.7, 150.9 and 201.2 MHz). The data were analyzed in terms of a frequency-dependent order parameter, S (2)(omega), to estimate the generalized order parameter and the contributions to the relaxation from different motional frequencies in the picosecond-nanosecond timescale and from any exchange processes that may be occurring on the microsecond-millisecond timescale. The relaxation data was surprisingly similar for spermine bound to two different duplexes and a linear parallel quadruplex. Analysis of the relaxation data from these complexes confirmed the conclusions of previous studies that the dominant motion of spermine is independent of the macroscopic tumbling of the DNA and has an effective correlation time of approximately 50 ps. In contrast, spermine bound to a folded antiparallel quadruplex had faster relaxation rates, especially R (2). As with the other complexes, a fast internal motion of the order of 50 ps makes a substantial contribution to the relaxation. The generalized order parameter for spermine bound to duplex DNA and the linear quadruplex is small but is larger for spermine bound to the folded quadruplex. In the latter case, there is evidence for exchange between at least two populations of spermine occurring on the microsecond-millisecond timescale.
@article{Keniry2007,
title = {An Investigation of the Dynamics of Spermine Bound to Duplex and Quadruplex {{DNA}} by (13){{C NMR}} Spectroscopy.},
author = {a Keniry, Max and a Owen, Elisabeth},
year = {2007},
month = jul,
journal = {European biophysics journal : EBJ},
volume = {36},
number = {6},
eprint = {17598053},
eprinttype = {pubmed},
pages = {637--46},
issn = {0175-7571},
doi = {10.1007/s00249-007-0136-4},
abstract = {A detailed analysis of the (13)C relaxation of (13)C-labelled spermine bound to duplex and quadruplex DNA is presented. T(1), T(2) and heteronuclear NOE data were collected at four (13)C frequencies (75.4, 125.7, 150.9 and 201.2 MHz). The data were analyzed in terms of a frequency-dependent order parameter, S (2)(omega), to estimate the generalized order parameter and the contributions to the relaxation from different motional frequencies in the picosecond-nanosecond timescale and from any exchange processes that may be occurring on the microsecond-millisecond timescale. The relaxation data was surprisingly similar for spermine bound to two different duplexes and a linear parallel quadruplex. Analysis of the relaxation data from these complexes confirmed the conclusions of previous studies that the dominant motion of spermine is independent of the macroscopic tumbling of the DNA and has an effective correlation time of approximately 50 ps. In contrast, spermine bound to a folded antiparallel quadruplex had faster relaxation rates, especially R (2). As with the other complexes, a fast internal motion of the order of 50 ps makes a substantial contribution to the relaxation. The generalized order parameter for spermine bound to duplex DNA and the linear quadruplex is small but is larger for spermine bound to the folded quadruplex. In the latter case, there is evidence for exchange between at least two populations of spermine occurring on the microsecond-millisecond timescale.},
pmid = {17598053},
keywords = {\#nosource,Carbon Isotopes,Carbon Isotopes: chemistry,G-Quadruplexes,Magnetic Resonance Spectroscopy,Nucleic Acid Conformation,Oligonucleotides,Oligonucleotides: chemistry,Spermine,Spermine: chemistry}
}
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The data were analyzed in terms of a frequency-dependent order parameter, S (2)(omega), to estimate the generalized order parameter and the contributions to the relaxation from different motional frequencies in the picosecond-nanosecond timescale and from any exchange processes that may be occurring on the microsecond-millisecond timescale. The relaxation data was surprisingly similar for spermine bound to two different duplexes and a linear parallel quadruplex. Analysis of the relaxation data from these complexes confirmed the conclusions of previous studies that the dominant motion of spermine is independent of the macroscopic tumbling of the DNA and has an effective correlation time of approximately 50 ps. In contrast, spermine bound to a folded antiparallel quadruplex had faster relaxation rates, especially R (2). As with the other complexes, a fast internal motion of the order of 50 ps makes a substantial contribution to the relaxation. The generalized order parameter for spermine bound to duplex DNA and the linear quadruplex is small but is larger for spermine bound to the folded quadruplex. In the latter case, there is evidence for exchange between at least two populations of spermine occurring on the microsecond-millisecond timescale.","pmid":"17598053","keywords":"#nosource,Carbon Isotopes,Carbon Isotopes: chemistry,G-Quadruplexes,Magnetic Resonance Spectroscopy,Nucleic Acid Conformation,Oligonucleotides,Oligonucleotides: chemistry,Spermine,Spermine: chemistry","bibtex":"@article{Keniry2007,\n title = {An Investigation of the Dynamics of Spermine Bound to Duplex and Quadruplex {{DNA}} by (13){{C NMR}} Spectroscopy.},\n author = {a Keniry, Max and a Owen, Elisabeth},\n year = {2007},\n month = jul,\n journal = {European biophysics journal : EBJ},\n volume = {36},\n number = {6},\n eprint = {17598053},\n eprinttype = {pubmed},\n pages = {637--46},\n issn = {0175-7571},\n doi = {10.1007/s00249-007-0136-4},\n abstract = {A detailed analysis of the (13)C relaxation of (13)C-labelled spermine bound to duplex and quadruplex DNA is presented. T(1), T(2) and heteronuclear NOE data were collected at four (13)C frequencies (75.4, 125.7, 150.9 and 201.2 MHz). The data were analyzed in terms of a frequency-dependent order parameter, S (2)(omega), to estimate the generalized order parameter and the contributions to the relaxation from different motional frequencies in the picosecond-nanosecond timescale and from any exchange processes that may be occurring on the microsecond-millisecond timescale. The relaxation data was surprisingly similar for spermine bound to two different duplexes and a linear parallel quadruplex. Analysis of the relaxation data from these complexes confirmed the conclusions of previous studies that the dominant motion of spermine is independent of the macroscopic tumbling of the DNA and has an effective correlation time of approximately 50 ps. In contrast, spermine bound to a folded antiparallel quadruplex had faster relaxation rates, especially R (2). 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