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. 1995 Aug;69(2):559–568. doi: 10.1016/S0006-3495(95)79929-5

Influence of counter-ions on the crystal structures of DNA decamers: binding of [Co(NH3)6]3+ and Ba2+ to A-DNA.

Y G Gao 1, H Robinson 1, J H van Boom 1, A H Wang 1
PMCID: PMC1236281  PMID: 8527670

Abstract

A-DNA is a stable alternative right-handed double helix that is favored by certain sequences (e.g., (dG)n.(dC)n) or under low humidity conditions. Earlier A-DNA structures of several DNA oligonucleotides and RNA.DNA chimeras have revealed some conformational variation that may be the result of sequence-dependent effects or crystal packing forces. In this study, four crystal structures of three decamer oligonucleotides, d(ACCGGCCGGT), d(ACCCGCGGGT), and r(GC)d(GTATACGC) in two crystal forms (either the P6(1)22 or the P2(1)2(1)2(1) space group) have been analyzed at high resolution to provide the molecular basis of the structural difference in an experimentally consistent manner. The study reveals that molecules crystallized in the same space group have a more similar A-DNA conformation, whereas the same molecule crystallized in different space groups has different (local) conformations. This suggests that even though the local structure is influenced by the crystal packing environments, the DNA molecule adjusts to adopt an overall conformation close to canonical A-DNA. For example, the six independent CpG steps in these four structures have different base-base stacking patterns, with their helical twist angles (omega) ranging from 28 degrees to 37 degrees. Our study further reveals the structural impact of different counter-ions on the A-DNA conformers. [Co(NH3)6]3+ has three unique A-DNA binding modes. One binds at the major groove side of a GpG step at the O6/N7 sites of guanine bases via hydrogen bonds. The other two modes involve the binding of ions to phosphates, either bridging across the narrow major groove or binding between two intra-strand adjacent phosphates. Those interactions may explain the recent spectroscopic and NMR observations that [Co(NH3)6]3+ is effective in inducing the B- to A-DNA transition for DNA with (G)n sequence. Interestingly, Ba2+ binds to the same O6/N7 sites on guanine by direct coordinations.

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Selected References

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  1. Baeyens K. J., De Bondt H. L., Holbrook S. R. Structure of an RNA double helix including uracil-uracil base pairs in an internal loop. Nat Struct Biol. 1995 Jan;2(1):56–62. doi: 10.1038/nsb0195-56. [DOI] [PubMed] [Google Scholar]
  2. Ban C., Ramakrishnan B., Sundaralingam M. A single 2'-hydroxyl group converts B-DNA to A-DNA. Crystal structure of the DNA-RNA chimeric decamer duplex d(CCGGC)r(G)d(CCGG) with a novel intermolecular G-C base-paired quadruplet. J Mol Biol. 1994 Feb 11;236(1):275–285. doi: 10.1006/jmbi.1994.1134. [DOI] [PubMed] [Google Scholar]
  3. Ban C., Ramakrishnan B., Sundaralingam M. Crystal structure of the highly distorted chimeric decamer r(C)d(CGGCGCCG)r(G).spermine complex--spermine binding to phosphate only and minor groove tertiary base-pairing. Nucleic Acids Res. 1994 Dec 11;22(24):5466–5476. doi: 10.1093/nar/22.24.5466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bassi G. S., Møllegaard N. E., Murchie A. I., von Kitzing E., Lilley D. M. Ionic interactions and the global conformations of the hammerhead ribozyme. Nat Struct Biol. 1995 Jan;2(1):45–55. doi: 10.1038/nsb0195-45. [DOI] [PubMed] [Google Scholar]
  5. Behe M., Felsenfeld G. Effects of methylation on a synthetic polynucleotide: the B--Z transition in poly(dG-m5dC).poly(dG-m5dC). Proc Natl Acad Sci U S A. 1981 Mar;78(3):1619–1623. doi: 10.1073/pnas.78.3.1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Behlen L. S., Sampson J. R., DiRenzo A. B., Uhlenbeck O. C. Lead-catalyzed cleavage of yeast tRNAPhe mutants. Biochemistry. 1990 Mar 13;29(10):2515–2523. doi: 10.1021/bi00462a013. [DOI] [PubMed] [Google Scholar]
  7. Benevides J. M., Wang A. H., Rich A., Kyogoku Y., van der Marel G. A., van Boom J. H., Thomas G. J., Jr Raman spectra of single crystals of r(GCG)d(CGC) and d(CCCCGGGG) as models for A DNA, their structure transitions in aqueous solution, and comparison with double-helical poly(dG).poly(dC). Biochemistry. 1986 Jan 14;25(1):41–50. doi: 10.1021/bi00349a007. [DOI] [PubMed] [Google Scholar]
  8. Bingman C. A., Zon G., Sundaralingam M. Crystal and molecular structure of the A-DNA dodecamer d(CCGTACGTACGG). Choice of fragment helical axis. J Mol Biol. 1992 Oct 5;227(3):738–756. doi: 10.1016/0022-2836(92)90221-5. [DOI] [PubMed] [Google Scholar]
  9. Braunlin W. H., Xu Q. Hexaamminecobalt(III) binding environments on double-helical DNA. Biopolymers. 1992 Dec;32(12):1703–1711. doi: 10.1002/bip.360321212. [DOI] [PubMed] [Google Scholar]
  10. Clark G. R., Brown D. G., Sanderson M. R., Chwalinski T., Neidle S., Veal J. M., Jones R. L., Wilson W. D., Zon G., Garman E. Crystal and solution structures of the oligonucleotide d(ATGCGCAT)2: a combined X-ray and NMR study. Nucleic Acids Res. 1990 Sep 25;18(18):5521–5528. doi: 10.1093/nar/18.18.5521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Cruse W. B., Saludjian P., Biala E., Strazewski P., Prangé T., Kennard O. Structure of a mispaired RNA double helix at 1.6-A resolution and implications for the prediction of RNA secondary structure. Proc Natl Acad Sci U S A. 1994 May 10;91(10):4160–4164. doi: 10.1073/pnas.91.10.4160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dock-Bregeon A. C., Chevrier B., Podjarny A., Johnson J., de Bear J. S., Gough G. R., Gilham P. T., Moras D. Crystallographic structure of an RNA helix: [U(UA)6A]2. J Mol Biol. 1989 Oct 5;209(3):459–474. doi: 10.1016/0022-2836(89)90010-7. [DOI] [PubMed] [Google Scholar]
  13. Duckett D. R., Murchie A. I., Lilley D. M. The role of metal ions in the conformation of the four-way DNA junction. EMBO J. 1990 Feb;9(2):583–590. doi: 10.1002/j.1460-2075.1990.tb08146.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Egli M., Usman N., Rich A. Conformational influence of the ribose 2'-hydroxyl group: crystal structures of DNA-RNA chimeric duplexes. Biochemistry. 1993 Apr 6;32(13):3221–3237. [PubMed] [Google Scholar]
  15. Frederick C. A., Quigley G. J., Teng M. K., Coll M., Van der Marel G. A., Van Boom J. H., Rich A., Wang A. H. Molecular structure of an A-DNA decamer d(ACCGGCCGGT). Eur J Biochem. 1989 May 1;181(2):295–307. doi: 10.1111/j.1432-1033.1989.tb14724.x. [DOI] [PubMed] [Google Scholar]
  16. Gao Y. G., Sriram M., Wang A. H. Crystallographic studies of metal ion-DNA interactions: different binding modes of cobalt(II), copper(II) and barium(II) to N7 of guanines in Z-DNA and a drug-DNA complex. Nucleic Acids Res. 1993 Aug 25;21(17):4093–4101. doi: 10.1093/nar/21.17.4093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gessner R. V., Quigley G. J., Wang A. H., van der Marel G. A., van Boom J. H., Rich A. Structural basis for stabilization of Z-DNA by cobalt hexaammine and magnesium cations. Biochemistry. 1985 Jan 15;24(2):237–240. doi: 10.1021/bi00323a001. [DOI] [PubMed] [Google Scholar]
  18. Haran T. E., Shakked Z., Wang A. H., Rich A. The crystal structure of d(CCCCGGGG): a new A-form variant with an extended backbone conformation. J Biomol Struct Dyn. 1987 Oct;5(2):199–217. doi: 10.1080/07391102.1987.10506390. [DOI] [PubMed] [Google Scholar]
  19. Heinemann U., Alings C., Bansal M. Double helix conformation, groove dimensions and ligand binding potential of a G/C stretch in B-DNA. EMBO J. 1992 May;11(5):1931–1939. doi: 10.1002/j.1460-2075.1992.tb05246.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Hingerty B. E., Brown R. S., Klug A. Stabilization of the tertiary structure of yeast phenylalanine tRNA by [Co(NH3)6]3+. X-ray evidence for hydrogen bonding to pairs of guanine bases in the major groove. Biochim Biophys Acta. 1982 Apr 26;697(1):78–82. doi: 10.1016/0167-4781(82)90047-1. [DOI] [PubMed] [Google Scholar]
  21. Ho P. S., Frederick C. A., Saal D., Wang A. H., Rich A. The interactions of ruthenium hexaammine with Z-DNA: crystal structure of a Ru(NH3)6+3 salt of d(CGCGCG) at 1.2 A resolution. J Biomol Struct Dyn. 1987 Feb;4(4):521–534. doi: 10.1080/07391102.1987.10507657. [DOI] [PubMed] [Google Scholar]
  22. Jia X., Marzilli L. G. Zinc ion-DNA polymer interactions. Biopolymers. 1991 Jan;31(1):23–44. doi: 10.1002/bip.360310104. [DOI] [PubMed] [Google Scholar]
  23. Kim J. L., Nikolov D. B., Burley S. K. Co-crystal structure of TBP recognizing the minor groove of a TATA element. Nature. 1993 Oct 7;365(6446):520–527. doi: 10.1038/365520a0. [DOI] [PubMed] [Google Scholar]
  24. Kim Y., Geiger J. H., Hahn S., Sigler P. B. Crystal structure of a yeast TBP/TATA-box complex. Nature. 1993 Oct 7;365(6446):512–520. doi: 10.1038/365512a0. [DOI] [PubMed] [Google Scholar]
  25. Laughlan G., Murchie A. I., Norman D. G., Moore M. H., Moody P. C., Lilley D. M., Luisi B. The high-resolution crystal structure of a parallel-stranded guanine tetraplex. Science. 1994 Jul 22;265(5171):520–524. doi: 10.1126/science.8036494. [DOI] [PubMed] [Google Scholar]
  26. 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]
  27. Peck L. J., Nordheim A., Rich A., Wang J. C. Flipping of cloned d(pCpG)n.d(pCpG)n DNA sequences from right- to left-handed helical structure by salt, Co(III), or negative supercoiling. Proc Natl Acad Sci U S A. 1982 Aug;79(15):4560–4564. doi: 10.1073/pnas.79.15.4560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Pley H. W., Flaherty K. M., McKay D. B. Three-dimensional structure of a hammerhead ribozyme. Nature. 1994 Nov 3;372(6501):68–74. doi: 10.1038/372068a0. [DOI] [PubMed] [Google Scholar]
  29. Ramakrishnan B., Sundaralingam M. Evidence for crystal environment dominating base sequence effects on DNA conformation: crystal structures of the orthorhombic and hexagonal polymorphs of the A-DNA decamer d(GCGGGCCCGC) and comparison with their isomorphous crystal structures. Biochemistry. 1993 Oct 26;32(42):11458–11468. doi: 10.1021/bi00093a025. [DOI] [PubMed] [Google Scholar]
  30. Ramakrishnan B., Sundaralingam M. High resolution crystal structure of the A-DNA decamer d(CCCGGCCGGG). Novel intermolecular base-paired G*(G.C) triplets. J Mol Biol. 1993 May 20;231(2):431–444. doi: 10.1006/jmbi.1993.1292. [DOI] [PubMed] [Google Scholar]
  31. Sauer R. T. Minor groove DNA-recognition by alpha-helices. Nat Struct Biol. 1995 Jan;2(1):7–9. doi: 10.1038/nsb0195-7. [DOI] [PubMed] [Google Scholar]
  32. Shakked Z., Rabinovich D., Kennard O., Cruse W. B., Salisbury S. A., Viswamitra M. A. Sequence-dependent conformation of an A-DNA double helix. The crystal structure of the octamer d(G-G-T-A-T-A-C-C). J Mol Biol. 1983 May 15;166(2):183–201. doi: 10.1016/s0022-2836(83)80005-9. [DOI] [PubMed] [Google Scholar]
  33. Steitz T. A. Structural studies of protein-nucleic acid interaction: the sources of sequence-specific binding. Q Rev Biophys. 1990 Aug;23(3):205–280. doi: 10.1017/s0033583500005552. [DOI] [PubMed] [Google Scholar]
  34. Valegård K., Murray J. B., Stockley P. G., Stonehouse N. J., Liljas L. Crystal structure of an RNA bacteriophage coat protein-operator complex. Nature. 1994 Oct 13;371(6498):623–626. doi: 10.1038/371623a0. [DOI] [PubMed] [Google Scholar]
  35. Verdaguer N., Aymami J., Fernández-Forner D., Fita I., Coll M., Huynh-Dinh T., Igolen J., Subirana J. A. Molecular structure of a complete turn of A-DNA. J Mol Biol. 1991 Sep 20;221(2):623–635. doi: 10.1016/0022-2836(91)80077-8. [DOI] [PubMed] [Google Scholar]
  36. Wang A. H., Fujii S., van Boom J. H., Rich A. Molecular structure of the octamer d(G-G-C-C-G-G-C-C): modified A-DNA. Proc Natl Acad Sci U S A. 1982 Jul;79(13):3968–3972. doi: 10.1073/pnas.79.13.3968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Weeks K. M., Crothers D. M. Major groove accessibility of RNA. Science. 1993 Sep 17;261(5128):1574–1577. doi: 10.1126/science.7690496. [DOI] [PubMed] [Google Scholar]
  38. Westhof E., Dumas P., Moras D. Crystallographic refinement of yeast aspartic acid transfer RNA. J Mol Biol. 1985 Jul 5;184(1):119–145. doi: 10.1016/0022-2836(85)90048-8. [DOI] [PubMed] [Google Scholar]
  39. Xu Q., Shoemaker R. K., Braunlin W. H. Induction of B-A transitions of deoxyoligonucleotides by multivalent cations in dilute aqueous solution. Biophys J. 1993 Sep;65(3):1039–1049. doi: 10.1016/S0006-3495(93)81163-9. [DOI] [PMC free article] [PubMed] [Google Scholar]

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