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. 1992 Mar 25;20(6):1223–1228. doi: 10.1093/nar/20.6.1223

The formation of A-DNA in NaDNA films is suppressed by netropsin.

H Fritzsche 1, R Brandes 1, A Rupprecht 1, Z Song 1, T Weidlich 1, D R Kearns 1
PMCID: PMC312162  PMID: 1313963

Abstract

Oriented films of NaDNA complexed with netropsin were studied with deuterium nuclear magnetic resonance (2H NMR), X-ray diffraction and ultraviolet (UV) linear dichroism to obtain information about the influence of netropsin on the structural arrangement of the DNA bases and on the B-A transition. The results of these studies clearly demonstrate a strong suppression of the formation of A-DNA at relative humidities (RHs) down to about 50%. The suppression was complete in the NaDNA-netropsin complex studied with 2H NMR which had a netropsin input ratio, r, of 0.22 drug/base pair. The sample used for UV linear dichroism had a similar input ratio while the X-ray diffraction samples had input ratios between 0.033 and 0.39 drug/base pair. Together, the results of these studies are in agreement with previous infrared (IR) linear dichroism studies of the conformation of the sugar-phosphate backbone in NaDNA-netropsin complexes, which showed that the B-A transition is suppressed for r-values down to approximately 0.1 drug/base pair (Fritzsche, H., Rupprecht, A. and Richter, M., Nucleic Acids Res. 12 (1984) 9165-9177).

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Selected References

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  1. Arnott S., Selsing E. The conformation of C-DNA. J Mol Biol. 1975 Oct 15;98(1):265–269. doi: 10.1016/s0022-2836(75)80115-x. [DOI] [PubMed] [Google Scholar]
  2. Brandes R., Ehrenberg A. Kinetics of the proton-deuteron exchange at position H8 of adenine and guanine in DNA. Nucleic Acids Res. 1986 Dec 9;14(23):9491–9508. doi: 10.1093/nar/14.23.9491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Brandes R., Rupprecht A., Kearns D. R. Interaction of water with oriented DNA in the A- and B-form conformations. Biophys J. 1989 Oct;56(4):683–691. doi: 10.1016/S0006-3495(89)82715-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brandes R., Vold R. R., Kearns D. R., Rupprecht A. A 2H-NMR study of the A-DNA conformation in films of oriented Na-DNA: evidence of a disordered B-DNA contribution. Biopolymers. 1988 Jul;27(7):1159–1170. doi: 10.1002/bip.360270709. [DOI] [PubMed] [Google Scholar]
  5. Brandes R., Vold R. R., Kearns D. R., Rupprecht A. Static disorder and librational motions of the purine bases in films of oriented Li-DNA. J Mol Biol. 1988 Jul 20;202(2):321–332. doi: 10.1016/0022-2836(88)90461-5. [DOI] [PubMed] [Google Scholar]
  6. Coll M., Aymami J., van der Marel G. A., van Boom J. H., Rich A., Wang A. H. Molecular structure of the netropsin-d(CGCGATATCGCG) complex: DNA conformation in an alternating AT segment. Biochemistry. 1989 Jan 10;28(1):310–320. doi: 10.1021/bi00427a042. [DOI] [PubMed] [Google Scholar]
  7. FULLER W., WILKINS M. H., WILSON H. R., HAMILTON L. D. THE MOLECULAR CONFIGURATION OF DEOXYRIBONUCLEIC ACID. IV. X-RAY DIFFRACTION STUDY OF THE A FORM. J Mol Biol. 1965 May;12:60–76. doi: 10.1016/s0022-2836(65)80282-0. [DOI] [PubMed] [Google Scholar]
  8. Forni A., Moretti I., Marconi G., Mongelli N., Samorí B. Linear dichroism studies of the complexes between CT-DNA and distamycins. Biopolymers. 1989 Dec;28(12):2177–2194. doi: 10.1002/bip.360281210. [DOI] [PubMed] [Google Scholar]
  9. Fritzsche H. Infrared studies of deoxyribonucleic acids, their constituents and analogues. 3. Evidence of slow isotopic exchange of hydrogen attached to carbon in DNA. Biochim Biophys Acta. 1967 Nov 21;149(1):173–179. doi: 10.1016/0005-2787(67)90699-5. [DOI] [PubMed] [Google Scholar]
  10. Fritzsche H., Rupprecht A. Modulation of the B-A transition of DNA by potential antitumor antibiotics. Influence of the base composition of DNA. J Biomol Struct Dyn. 1990 Apr;7(5):1135–1140. doi: 10.1080/07391102.1990.10508551. [DOI] [PubMed] [Google Scholar]
  11. Fritzsche H., Rupprecht A., Richter M. Infrared linear dichroism of oriented DNA-ligand complexes prepared with the wet-spinning method. Nucleic Acids Res. 1984 Dec 11;12(23):9165–9177. doi: 10.1093/nar/12.23.9165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Higuchi S., Tsuboi M., Iitaka Y. Infrared spectrum of a DNA-RNA hybrid. Biopolymers. 1969;7(6):909–916. doi: 10.1002/bip.1969.360070606. [DOI] [PubMed] [Google Scholar]
  13. Ivanov V. I., Minchenkova L. E., Schyolkina A. K., Poletayev A. I. Different conformations of double-stranded nucleic acid in solution as revealed by circular dichroism. Biopolymers. 1973;12(1):89–110. doi: 10.1002/bip.1973.360120109. [DOI] [PubMed] [Google Scholar]
  14. Kopka M. L., Yoon C., Goodsell D., Pjura P., Dickerson R. E. Binding of an antitumor drug to DNA, Netropsin and C-G-C-G-A-A-T-T-BrC-G-C-G. J Mol Biol. 1985 Jun 25;183(4):553–563. doi: 10.1016/0022-2836(85)90171-8. [DOI] [PubMed] [Google Scholar]
  15. Kopka M. L., Yoon C., Goodsell D., Pjura P., Dickerson R. E. The molecular origin of DNA-drug specificity in netropsin and distamycin. Proc Natl Acad Sci U S A. 1985 Mar;82(5):1376–1380. doi: 10.1073/pnas.82.5.1376. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lindsay S. M., Lee S. A., Powell J. W., Weidlich T., DeMarco C., Lewen G. D., Tao N. J., Rupprecht A. The origin of the A to B transition in DNA fibers and films. Biopolymers. 1988 Jun;27(6):1015–1043. doi: 10.1002/bip.360270610. [DOI] [PubMed] [Google Scholar]
  17. MARVIN D. A., SPENCER M., WILKINS M. H., HAMILTON L. D. The molecular configuration of deoxyribonucleic acid. III. X-ray diffraction study of the C form of the lithium salt. J Mol Biol. 1961 Oct;3:547–565. doi: 10.1016/s0022-2836(61)80021-1. [DOI] [PubMed] [Google Scholar]
  18. Malenkov G., Minchenkova L., Minyat E., Schyolkina A., Ivanov V. The nature of the B-A transition of DNA in solution. FEBS Lett. 1975 Mar 1;51(1):38–42. doi: 10.1016/0014-5793(75)80850-7. [DOI] [PubMed] [Google Scholar]
  19. McCall M., Brown T., Hunter W. N., Kennard O. The crystal structure of d(GGATGGGAG): an essential part of the binding site for transcription factor IIIA. Nature. 1986 Aug 14;322(6080):661–664. doi: 10.1038/322661a0. [DOI] [PubMed] [Google Scholar]
  20. Mohr S. C., Sokolov N. V., He C. M., Setlow P. Binding of small acid-soluble spore proteins from Bacillus subtilis changes the conformation of DNA from B to A. Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):77–81. doi: 10.1073/pnas.88.1.77. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pohle W., Fritzsche H. A new conformation-specific infrared band of A-DNA in films. Nucleic Acids Res. 1980 Jun 11;8(11):2527–2535. doi: 10.1093/nar/8.11.2527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Pohle W., Zhurkin V. B., Fritzsche H. The DNA phosphate orientation. Infrared data and energetically favorable structures. Biopolymers. 1984 Nov;23(11 Pt 2):2603–2622. doi: 10.1002/bip.360231131. [DOI] [PubMed] [Google Scholar]
  23. Rhodes D., Klug A. An underlying repeat in some transcriptional control sequences corresponding to half a double helical turn of DNA. Cell. 1986 Jul 4;46(1):123–132. doi: 10.1016/0092-8674(86)90866-4. [DOI] [PubMed] [Google Scholar]
  24. Rupprecht A. A wet spinning apparatus and auxiliary equipment suitable for preparing samples of oriented DNA. Biotechnol Bioeng. 1970 Jan;12(1):93–121. doi: 10.1002/bit.260120109. [DOI] [PubMed] [Google Scholar]
  25. Rupprecht A., Forslind B. Variation of electrolyte content in wet-spun lithium- and sodium-DNA. Biochim Biophys Acta. 1970 Apr 15;204(2):304–316. doi: 10.1016/0005-2787(70)90148-6. [DOI] [PubMed] [Google Scholar]
  26. Rupprecht A. Preparation of oriented DNA by wet spinning. Acta Chem Scand. 1966;20(2):494–504. doi: 10.3891/acta.chem.scand.20-0494. [DOI] [PubMed] [Google Scholar]
  27. SPENCER M., FULLER W., WILKINS M. H., BROWN G. L. Determination of the helical configuration of ribonucleic acid molecules by X-ray diffraction study of crystalline amino-acid-transfer ribonucleic acid. Nature. 1962 Jun 16;194:1014–1020. doi: 10.1038/1941014a0. [DOI] [PubMed] [Google Scholar]
  28. Wartell R. M., Larson J. E., Wells R. D. Netropsin. A specific probe for A-T regions of duplex deoxyribonucleic acid. J Biol Chem. 1974 Nov 10;249(21):6719–6731. [PubMed] [Google Scholar]
  29. Wähnert U., Zimmer O., Luck G., Pitra O. (dA-dT) dependent inactivation of the DNA template properties by interaction with netropsin and distamycin A. Nucleic Acids Res. 1975 Mar;2(3):391–404. doi: 10.1093/nar/2.3.391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Zasedatelev A. S., Gursky G. V., Zimmer C., Thrum H. Binding of netropsin to DNA and synthetic polynucleotides. Mol Biol Rep. 1974 Mar;1(6):337–342. doi: 10.1007/BF00309567. [DOI] [PubMed] [Google Scholar]
  31. Zimmer C. Effects of the antibiotics netropsin and distamycin A on the structure and function of nucleic acids. Prog Nucleic Acid Res Mol Biol. 1975;15(0):285–318. doi: 10.1016/s0079-6603(08)60122-1. [DOI] [PubMed] [Google Scholar]

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