Abstract
One- and two-dimensional 1H NMR spectroscopy were used to characterize the binding of a homodimeric thiazole orange dye, 1,1'-(4,4,8,8-tetramethyl-4,8-diazaundecamethylene)-bis-4-(3 -methyl-2,3-dihydro-(benzo- 1,3-thiazole)-2-methylidene)-quinolinium tetraiodide (TOTO), to various double-stranded DNA oligonucleotides containing symmetric (5'-pyr-pyr-pu-pu-3')2 or (5'-pu-pu-pyr-pyr-3')2 sequences. It was found that TOTO binds preferentially to oligonucleotides containing a (5'-CTAG-3')2 or a (5'-CCGG-3')2 sequence. Binding to the (5'-CCGG-3')2 sequence is less favored than to the (5'-CTAG-3')2 sequence. The complexes of TOTO with d(CGCTAGCGCTAGCG)2 (10) and d(CGCTAGCCGGCG):d(CGCCGGCTAGCG) (11) oligonucleotides, each containing two preferential binding sites, was also examined. In both cases TOTO forms mixtures of 1:1 and 1:2 dsDNA-TOTO complexes in ratios dependent on the relative amount of TOTO and the oligonucleotides in the sample. Binding of TOTO to the two oligonucleotides is sequence selective at the (5'-CTAG-3')2 and (5'-CCGG-3')2 sites. The 1H NMR spectra of both the 1:2 complexes and the three different 1:1 complexes have been assigned. A slight negative cooperativity is observed in formation of the 1:2 complexes. The ratio between the two different 1:1 complexes formed with oligonucleotide 11 is 2.4 in favor of binding to the (5'-CTAG-3')2 site. This is very similar to results obtained when the two sites are in different oligonucleotides. Thus the distribution of TOTO among the (5'-CTAG-3')2 and (5'-CCGG-3')2 sites is independent of whether the two sites are in the same or two different oligonucleotides.
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Selected References
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- Addess K. J., Feigon J. Sequence specificity of quinoxaline antibiotics. 1. Solution structure of a 1:1 complex between triostin A and [d(GACGTC)]2 and comparison with the solution structure of the [N-MeCys3,N-MeCys7]TANDEM-[d(GATATC)]2 complex. Biochemistry. 1994 Oct 18;33(41):12386–12396. doi: 10.1021/bi00207a005. [DOI] [PubMed] [Google Scholar]
- Addess K. J., Feigon J. Sequence specificity of quinoxaline antibiotics. 2. NMR studies of the binding of [N-MeCys3,N-MeCys7]TANDEM and triostin A to DNA containing a CpI step. Biochemistry. 1994 Oct 18;33(41):12397–12404. doi: 10.1021/bi00207a006. [DOI] [PubMed] [Google Scholar]
- Addess K. J., Gilbert D. E., Olsen R. K., Feigon J. Proton NMR studies of [N-MeCys3,N-MeCys7]TANDEM binding to DNA oligonucleotides: sequence-specific binding at the TpA site. Biochemistry. 1992 Jan 21;31(2):339–350. doi: 10.1021/bi00117a005. [DOI] [PubMed] [Google Scholar]
- Bailly C., Hénichart J. P. DNA recognition by intercalator-minor-groove binder hybrid molecules. Bioconjug Chem. 1991 Nov-Dec;2(6):379–393. doi: 10.1021/bc00012a001. [DOI] [PubMed] [Google Scholar]
- Benson S. C., Mathies R. A., Glazer A. N. Heterodimeric DNA-binding dyes designed for energy transfer: stability and applications of the DNA complexes. Nucleic Acids Res. 1993 Dec 11;21(24):5720–5726. doi: 10.1093/nar/21.24.5720. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benson S. C., Singh P., Glazer A. N. Heterodimeric DNA-binding dyes designed for energy transfer: synthesis and spectroscopic properties. Nucleic Acids Res. 1993 Dec 11;21(24):5727–5735. doi: 10.1093/nar/21.24.5727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Delepierre M., Dinh T. H., Roques B. P. Bisintercalation of ditercalinium into a d(CpGpApTpCpG)2 minihelix: a 1H- and 31P-NMR study. Biopolymers. 1989 Dec;28(12):2115–2142. doi: 10.1002/bip.360281207. [DOI] [PubMed] [Google Scholar]
- Delepierre M., Maroun R., Garbay-Jaureguiberry C., Igolen J., Roques B. P. 1H and 31P nuclear magnetic resonance studies of the differences in DNA deformation induced by anti-tumoral 7H-pyrido[4,3-c]carbazole dimers. J Mol Biol. 1989 Nov 5;210(1):211–228. doi: 10.1016/0022-2836(89)90301-x. [DOI] [PubMed] [Google Scholar]
- Delepierre M., Milhe C., Namane A., Dinh T. H., Roques B. P. 1H- and 31P-NMR studies of ditercalinium binding to a d(GCGC)2 and d(CCTATAGG)2 minihelices: a sequence specificity study. Biopolymers. 1991 Feb 15;31(3):331–353. doi: 10.1002/bip.360310307. [DOI] [PubMed] [Google Scholar]
- Feigon J., Leupin W., Denny W. A., Kearns D. R. Two-dimensional proton nuclear magnetic resonance investigation of the synthetic deoxyribonucleic acid decamer d(ATATCGATAT)2. Biochemistry. 1983 Dec 6;22(25):5943–5951. doi: 10.1021/bi00294a038. [DOI] [PubMed] [Google Scholar]
- Gao X. L., Patel D. J. Antitumour drug-DNA interactions: NMR studies of echinomycin and chromomycin complexes. Q Rev Biophys. 1989 May;22(2):93–138. doi: 10.1017/s0033583500003814. [DOI] [PubMed] [Google Scholar]
- Gilbert D. E., Feigon J. Proton NMR study of the [d(ACGTATACGT)]2-2echinomycin complex: conformational changes between echinomycin binding sites. Nucleic Acids Res. 1992 May 25;20(10):2411–2420. doi: 10.1093/nar/20.10.2411. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gilbert D. E., Feigon J. The DNA sequence at echinomycin binding sites determines the structural changes induced by drug binding: NMR studies of echinomycin binding to [d(ACGTACGT)]2 and [d(TCGATCGA)]2. Biochemistry. 1991 Mar 5;30(9):2483–2494. doi: 10.1021/bi00223a027. [DOI] [PubMed] [Google Scholar]
- Gilbert D. E., van der Marel G. A., van Boom J. H., Feigon J. Unstable Hoogsteen base pairs adjacent to echinomycin binding sites within a DNA duplex. Proc Natl Acad Sci U S A. 1989 May;86(9):3006–3010. doi: 10.1073/pnas.86.9.3006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hare D. R., Wemmer D. E., Chou S. H., Drobny G., Reid B. R. Assignment of the non-exchangeable proton resonances of d(C-G-C-G-A-A-T-T-C-G-C-G) using two-dimensional nuclear magnetic resonance methods. J Mol Biol. 1983 Dec 15;171(3):319–336. doi: 10.1016/0022-2836(83)90096-7. [DOI] [PubMed] [Google Scholar]
- Jacobsen J. P., Pedersen J. B., Hansen L. F., Wemmer D. E. Site selective bis-intercalation of a homodimeric thiazole orange dye in DNA oligonucleotides. Nucleic Acids Res. 1995 Mar 11;23(5):753–760. doi: 10.1093/nar/23.5.753. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maroun R., Delepierre M., Roques B. P. Intercalative binding of ditercalinium to d(CpGpCpG)2: a theoretical study. J Biomol Struct Dyn. 1989 Dec;7(3):607–621. doi: 10.1080/07391102.1989.10508510. [DOI] [PubMed] [Google Scholar]
- Mouscadet J. F., Ketterlé C., Goulaouic H., Carteau S., Subra F., Le Bret M., Auclair C. Triple helix formation with short oligonucleotide-intercalator conjugates matching the HIV-1 U3 LTR end sequence. Biochemistry. 1994 Apr 12;33(14):4187–4196. doi: 10.1021/bi00180a011. [DOI] [PubMed] [Google Scholar]
- Orson F. M., Kinsey B. M., McShan W. M. Linkage structures strongly influence the binding cooperativity of DNA intercalators conjugated to triplex forming oligonucleotides. Nucleic Acids Res. 1994 Feb 11;22(3):479–484. doi: 10.1093/nar/22.3.479. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perkins T. T., Quake S. R., Smith D. E., Chu S. Relaxation of a single DNA molecule observed by optical microscopy. Science. 1994 May 6;264(5160):822–826. doi: 10.1126/science.8171336. [DOI] [PubMed] [Google Scholar]
- Perkins T. T., Smith D. E., Chu S. Direct observation of tube-like motion of a single polymer chain. Science. 1994 May 6;264(5160):819–822. doi: 10.1126/science.8171335. [DOI] [PubMed] [Google Scholar]
- Pothier J., Delepierre M., Barsi M. C., Garbay-Jaureguiberry C., Igolen J., Le Bret M., Roques B. P. Comparison of the bis-intercalating complexes formed between either ditercalinium or a flexible analogue and d(CpGpCpG)2 or d(TpTpCpGpCpGpApA)2 minihelices: 1H- and 31P-NMR analyses. Biopolymers. 1991 Oct;31(11):1309–1323. doi: 10.1002/bip.360311109. [DOI] [PubMed] [Google Scholar]
- Rye H. S., Dabora J. M., Quesada M. A., Mathies R. A., Glazer A. N. Fluorometric assay using dimeric dyes for double- and single-stranded DNA and RNA with picogram sensitivity. Anal Biochem. 1993 Jan;208(1):144–150. doi: 10.1006/abio.1993.1020. [DOI] [PubMed] [Google Scholar]
- Rye H. S., Yue S., Quesada M. A., Haugland R. P., Mathies R. A., Glazer A. N. Picogram detection of stable dye-DNA intercalation complexes with two-color laser-excited confocal fluorescence gel scanner. Methods Enzymol. 1993;217:414–431. doi: 10.1016/0076-6879(93)17080-o. [DOI] [PubMed] [Google Scholar]
- Rye H. S., Yue S., Wemmer D. E., Quesada M. A., Haugland R. P., Mathies R. A., Glazer A. N. Stable fluorescent complexes of double-stranded DNA with bis-intercalating asymmetric cyanine dyes: properties and applications. Nucleic Acids Res. 1992 Jun 11;20(11):2803–2812. doi: 10.1093/nar/20.11.2803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scheek R. M., Boelens R., Russo N., van Boom J. H., Kaptein R. Sequential resonance assignments in 1H NMR spectra of oligonucleotides by two-dimensional NMR spectroscopy. Biochemistry. 1984 Mar 27;23(7):1371–1376. doi: 10.1021/bi00302a006. [DOI] [PubMed] [Google Scholar]
- Searle M. S., Hall J. G., Denny W. A., Wakelin L. P. Interaction of the antitumour antibiotic luzopeptin with the hexanucleotide duplex d(5'-GCATGC)2. One-dimensional and two-dimensional n.m.r. studies. Biochem J. 1989 Apr 15;259(2):433–441. doi: 10.1042/bj2590433. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spielmann H. P., Wemmer D. E., Jacobsen J. P. Solution structure of a DNA complex with the fluorescent bis-intercalator TOTO determined by NMR spectroscopy. Biochemistry. 1995 Jul 11;34(27):8542–8553. doi: 10.1021/bi00027a004. [DOI] [PubMed] [Google Scholar]
- Subra F., Carteau S., Pager J., Paoletti J., Paoletti C., Auclair C., Mrani D., Gosselin G., Imbach J. L. Bis(pyrrolecarboxamide) linked to intercalating chromophore oxazolopyridocarbazole (OPC): selective binding to DNA and polynucleotides. Biochemistry. 1991 Feb 12;30(6):1642–1650. doi: 10.1021/bi00220a029. [DOI] [PubMed] [Google Scholar]
- Williams L. D., Gao Q. DNA-ditercalinium interactions: implications for recognition of damaged DNA. Biochemistry. 1992 May 5;31(17):4315–4324. doi: 10.1021/bi00132a024. [DOI] [PubMed] [Google Scholar]
