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  • 2010-2014  (2)
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  • 1
    Publication Date: 2013-08-28
    Description: The 2'-deoxynucleoside containing the synthetic base 1-[(2 R ,4 S ,5 R )-4-hydroxy-5-(hydroxymethyl)-tetrahydrofuran-2-yl)-1 H -perimidin-2(3 H )-one] (dPer) recognizes in DNA the O 6 -benzyl-2'-deoxyguanosine nucleoside ( O 6 -Bn-dG), formed by exposure to N -benzylmethylnitrosamine. Herein, we show how dPer distinguishes between O 6 -Bn-dG and dG in DNA. The structure of the modified Dickerson–Drew dodecamer (DDD) in which guanine at position G 4 has been replaced by O 6 -Bn-dG and cytosine C 9 has been replaced with dPer to form the modified O 6 -Bn-dG:dPer (DDD-XY) duplex [5'-d(C 1 G 2 C 3 X 4 A 5 A 6 T 7 T 8 Y 9 G 10 C 11 G 12 )-3'] 2 ( X = O 6 -Bn-dG, Y = dPer) reveals that dPer intercalates into the duplex and adopts the syn conformation about the glycosyl bond. This provides a binding pocket that allows the benzyl group of O 6 -Bn-dG to intercalate between Per and thymine of the 3'-neighbor A:T base pair. Nuclear magnetic resonance data suggest that a similar intercalative recognition mechanism applies in this sequence in solution. However, in solution, the benzyl ring of O 6 -Bn-dG undergoes rotation on the nuclear magnetic resonance time scale. In contrast, the structure of the modified DDD in which cytosine at position C 9 is replaced with dPer to form the dG:dPer (DDD-GY) [5'-d(C 1 G 2 C 3 G 4 A 5 A 6 T 7 T 8 Y 9 G 10 C 11 G 12 )-3'] 2 duplex ( Y = dPer) reveals that dPer adopts the anti conformation about the glycosyl bond and forms a less stable wobble pairing interaction with guanine.
    Print ISSN: 0305-1048
    Electronic ISSN: 1362-4962
    Topics: Biology
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  • 2
    Publication Date: 2010-07-09
    Description: The crystal structure of the nonstoichiometric complex of gramicidin D with NaI has been studied using synchrotron radiation at 100 K. The limiting resolution was 1.25 Å and theRfactor was 16% for 19 883 observed reflections. The general architecture of the antiparallel two-stranded gramicidin dimers in the studied crystal was a right-handed antiparallel double-stranded form that closely resembles the structures of other right-handed species published to date. However, there were several surprising observations. In addition to the significantly different composition of linear gramicidins identified in the crystal structure, including the absence of the gramicidin C form, only two cationic sites were found in each of the two independent dimers (channels), which were partially occupied by sodium, compared with the seven sites found in the RbCl complex of gramicidin. The sum of the partial occupancies of Na+was only 1.26 per two dimers and was confirmed by the similar content of iodine ions (1.21 ions distributed over seven sites), which was easily visible from their anomalous signal. Another surprising observation was the significant asymmetry of the distributions and occupancies of cations in the gramicidin dimers, which was in contrast to those observed in the high-resolution structures of the complexes of heavier alkali metals with gramicidin D, especially that of rubidium.
    Print ISSN: 0907-4449
    Electronic ISSN: 1399-0047
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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