Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1993 Aug 25;21(17):4127–4132. doi: 10.1093/nar/21.17.4127

Helical nature of poly(dI-dC).poly(dI-dC). Vibrational circular dichroism results.

L Wang 1, T A Keiderling 1
PMCID: PMC310019  PMID: 8371987

Abstract

Poly(dI-dC).poly(dI-dC) was studied using vibrational circular dichroism and IR spectroscopy in both the base deformation C = O and symmetric PO2- stretching regions. VCD spectra of this duplex under low salt conditions are consistent with its having a B-form structure. Addition of 5 M NaCl leads to relatively uniform VCD intensity loss which is consistent with loss of helical structure rather than formation of an intermediate state between the B and Z forms. This duplex polymer under high salt conditions with added NiCl2 shows aggregation effects, but its IR and VCD spectra have characteristic features of the Z-form DNA conformation. The cooperative change of backbone and base pair structure upon thermal denaturation is indicated by the simultaneous collapse of the VCD at 65 degrees C in both the PO2- and C = O stretching regions. This study further demonstrates that the VCD bandshape of a specific localized nucleic acid vibrational transition can be a useful indicator of the helical handedness. The empirical conformational interpretations are supported by simulated VCD spectra, which are in excellent agreement with the experimental results, based on dipole coupling calculations.

Full text

PDF
4127

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnott S., Chandrasekaran R., Hukins D. W., Smith P. J., Watts L. Structural details of double-helix observed for DNAs containing alternating purine and pyrimidine sequences. J Mol Biol. 1974 Sep 15;88(2):523–533. doi: 10.1016/0022-2836(74)90499-9. [DOI] [PubMed] [Google Scholar]
  2. Cohen J. S., Wooten J. B., Chatterjee C. L. Characterization of alternating deoxyribonucleic acid conformations in solution by phosphorus-31 nuclear magnetic resonance spectroscopy. Biochemistry. 1981 May 26;20(11):3049–3055. doi: 10.1021/bi00514a010. [DOI] [PubMed] [Google Scholar]
  3. DAVIES D. R., BALDWIN R. L. X-ray studies on two synthetic DNA copolymers. J Mol Biol. 1963 Apr;6:251–255. doi: 10.1016/s0022-2836(63)80086-8. [DOI] [PubMed] [Google Scholar]
  4. Drew H. R., Dickerson R. E. A new model for DNA containing A.T and I.C base pairs. EMBO J. 1982;1(6):663–667. doi: 10.1002/j.1460-2075.1982.tb01227.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gulotta M., Goss D. J., Diem M. IR vibrational CD in model deoxyoligonucleotides: observation of the B----Z phase transition and extended coupled oscillator intensity calculations. Biopolymers. 1989 Dec;28(12):2047–2058. doi: 10.1002/bip.360281202. [DOI] [PubMed] [Google Scholar]
  6. Mirau P. A., Kearns D. R. Comparison of the conformation of poly(dI-dC) with poly(dI-dbr5C) and the B and Z forms of poly(dG-dC). One- and two-dimensional NMR studies. Biochemistry. 1984 Nov 6;23(23):5439–5446. doi: 10.1021/bi00318a010. [DOI] [PubMed] [Google Scholar]
  7. Mitsui Y., Langridge R., Shortle B. E., Cantor C. R., Grant R. C., Kodama M., Wells R. D. Physical and enzymatic studies on poly d(I-C)-poly d(I-C), an unusual double-helical DNA. Nature. 1970 Dec 19;228(5277):1166–1169. doi: 10.1038/2281166a0. [DOI] [PubMed] [Google Scholar]
  8. Pohl F. M., Jovin T. M. Salt-induced co-operative conformational change of a synthetic DNA: equilibrium and kinetic studies with poly (dG-dC). J Mol Biol. 1972 Jun 28;67(3):375–396. doi: 10.1016/0022-2836(72)90457-3. [DOI] [PubMed] [Google Scholar]
  9. Ramaswamy N., Bansal M., Gupta G., Sasisekharan V. Left-handed helices for DNA: studies on poly[d(I-C)]. Proc Natl Acad Sci U S A. 1982 Oct;79(20):6109–6113. doi: 10.1073/pnas.79.20.6109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Rao M. V., Atreyi M., Kumar G. S., Kumar S. Reversal of the long-wavelength CD band of poly(dI-dC).poly(dI-dC) on specific interaction with the 53-58 peptide fragment of the lac repressor. Biopolymers. 1987 Mar;26(3):329–332. doi: 10.1002/bip.360260302. [DOI] [PubMed] [Google Scholar]
  11. Riazance J. H., Baase W. A., Johnson W. C., Jr, Hall K., Cruz P., Tinoco I., Jr Evidence for Z-form RNA by vacuum UV circular dichroism. Nucleic Acids Res. 1985 Jul 11;13(13):4983–4989. doi: 10.1093/nar/13.13.4983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Sutherland J. C., Griffin K. P., Keck P. C., Takacs P. Z. Z-DNA: vacuum ultraviolet circular dichroism. Proc Natl Acad Sci U S A. 1981 Aug;78(8):4801–4804. doi: 10.1073/pnas.78.8.4801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Vorlícková M., Sági J. Transitions of poly(dI-dC), poly(dI-methyl5dC) and poly(dI-bromo5dC) among and within the B-, Z-, A- and X-DNA families of conformations. Nucleic Acids Res. 1991 May 11;19(9):2343–2347. doi: 10.1093/nar/19.9.2343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Wang L., Keiderling T. A. Vibrational circular dichroism studies of the A-to-B conformational transition in DNA. Biochemistry. 1992 Oct 27;31(42):10265–10271. doi: 10.1021/bi00157a013. [DOI] [PubMed] [Google Scholar]
  15. Williams A. L., Jr, Cheong C., Tinoco I., Jr, Clark L. B. Vacuum ultraviolet circular dichroism as an indicator of helical handedness in nucleic acids. Nucleic Acids Res. 1986 Aug 26;14(16):6649–6659. doi: 10.1093/nar/14.16.6649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Yang L., Keiderling T. A. Vibrational CD study of the thermal denaturation of poly(rA).poly(rU). Biopolymers. 1993 Feb;33(2):315–327. doi: 10.1002/bip.360330213. [DOI] [PubMed] [Google Scholar]
  17. Zhong W. X., Gulotta M., Goss D. J., Diem M. DNA solution conformation via infrared circular dichroism: experimental and theoretical results for B-family polymers. Biochemistry. 1990 Aug 14;29(32):7485–7491. doi: 10.1021/bi00484a018. [DOI] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES