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NMR with 13C, 15N-doubly-labeled DNA: The shape Antennapedia homeodomain complex with a 14-mer DNA duplex

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Abstract

Nearly complete 1H, 13C and15 N NMR assignments have been obtained for a doubly labeled 14-base pair DNA duplex in solution both in the free state and complexed with the uniformly 15N-labeled Antennapedia homeodomain. The DNA was either fully 13C,15N-labeled or contained uniformly 13C, 15N-labeled nucleotides only at those positions which form the protein–DNA interface in the previously determined NMR solution structure of the Antennapedia homeodomain–DNA complex. The resonance assignments were obtained in three steps: (i) identification of the deoxyribose spin systems via scalar couplings using 2D and 3D HCCH-COSY and soft-relayed HCCH-COSY; (ii) sequential assignment of the nucleotides via1 H–1H NOEs observed in 3D13 C-resolved NOESY; and (iii) assignment of the imino and amino groups via 1H–1H NOEs and15 N–1H correlation spectroscopy. The assignment of the duplex in the 17 kDa protein–DNA complex was greatly facilitated by the fact that 1H signals of the protein were filtered out in 13C-resolved spectroscopy and by the excellent carbon chemical shift dispersion of the DNA duplex. Comparison of corresponding 13C chemical shifts of the free and the protein-bound DNA indicates conformational changes in the DNA upon complex formation.

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References

  • Allain, F.H.T., Gubser, C.C., Howe, P.W.A., Nagai, K., Neuhaus, D. and Varani, G. (1996) Nature, 380, 646–650.

    Google Scholar 

  • Anil Kumar, Ernst, R.R. and Wüthrich, K. (1980) Biochem. Biophys. Res. Commun, 95, 1–6.

    Google Scholar 

  • Bartels, C., Xia, T., Billeter, M., Güntert, P. and Wüthrich, K. (1995) J. Biomol. NMR, 6, 1–10.

    Google Scholar 

  • Billeter, M., Qian, Y.Q., Otting, G., Müller, M., Gehring, W. and Wüthrich, K. (1993) J. Mol. Biol., 234, 1084–1097.

    Google Scholar 

  • Billeter, M., Güntert, P., Luginbühl, P. and Wüthrich, K. (1996) Cell, 85, 1057–1065.

    Google Scholar 

  • Bodenhausen, G. and Ruben, D. (1980) Chem. Phys. Lett., 69, 185–188.

    Google Scholar 

  • Chazin, W.J., Wüthrich, K., Hyberts, S., Rance, M., Denny, W.A. and Leupin, W. (1986) J. Mol. Biol., 190, 439–453.

    Google Scholar 

  • Dieckmann, T. and Feigon, J. (1994) Curr. Opin Struct. Biol., 4, 745–749.

    Google Scholar 

  • Feigon, J., Leupin, W., Denny, W.A. and Kearns, D.R. (1983) Biochemistry, 22, 5943–5951.

    Google Scholar 

  • Frechet, D., Cheng, D.M., Kan, L.S. and Ts'o, P.O.P. (1983) Biochemistry, 22, 5194–5200.

    Google Scholar 

  • Geen, H. and Freeman, R. (1991) J. Magn. Reson., 93, 93–96.

    Google Scholar 

  • Ghose, R., Marino, J.P., Wiberg, K.B. and Prestegard, J.H. (1994)J. Am. Chem. Soc., 116, 8827–8828.

    Google Scholar 

  • Grzesiek, S., Kuboniwa, H., Hinck, A.P. and Bax, A. (1995) J. Am. Chem. Soc., 117, 5312–5315.

    Google Scholar 

  • Güntert, P., Dötsch, V., Wider, G. and Wüthrich, K. (1992) J. Biomol. NMR, 2, 619–629.

    Google Scholar 

  • Haasnoot C.A.G., Westering, H.P., van der Marel, G.A. and van Boom, J.H. (1983) J. Biomol. Struct. Dyn., 1, 131–149.

    Google Scholar 

  • Hare, D.R., Wemmer, D.E., Chou, S.H., Drobny, G. and Reid, B.R. (1983) J. Mol. Biol., 171, 319–336.

    Google Scholar 

  • Ikura, M., Kay, L.E., Tschudin, R. and Bax, A. (1990) J. Magn. Reson., 86, 204–209.

    Google Scholar 

  • Ikura, M., Kay, L.E. and Bax, A. (1991) J. Biomol. NMR, 1, 299–304.

    Google Scholar 

  • Kainosho, M. (1997) Nat. Struct. Biol., 4, 858–861.

    Google Scholar 

  • Legault, P., Jucker, F.M. and Pardi, A. (1995) FEBS Lett., 362, 156–160.

    Google Scholar 

  • Marion, D., Ikura, K., Tschudin, R. and Bax, A. (1989) J. Magn. Reson., 85, 393–399.

    Google Scholar 

  • Mueller, L., Legault, P. and Pardi, A. (1995) J. Am. Chem. Soc., 117, 11043–11048.

    Google Scholar 

  • Müller, M., Affolter, M., Leupin, W., Otting, G., Wüthrich, K. and Gehring, W.J. (1988) EMBO J., 7, 4299–4304.

    Google Scholar 

  • Nikonowicz, E.P. and Pardi, A. (1993) J. Mol. Biol., 232, 1141–1156.

    Google Scholar 

  • Oldfield, E. (1995) J. Biomol. NMR, 5, 217–225.

    Google Scholar 

  • Omichinski, J., Pedone, P.V., Felsenfeld, G., Gronenborn, A. and Clore, G.M. (1997) Nat. Struct. Biol., 122–132.

  • Ono, A., Tate, S. and Kainosho, M. (1994b) In Stable Isotope Applications in Biomolecular Structure and Mechanisms (Eds., Trewhella, J., Cross, T.A. and Unkefer, C.J.), Los Alamos National Laboratory New Mexico, pp. 127–144.

    Google Scholar 

  • Ono, A., Tate, S., Ishido, Y. and Kainosho, M. (1994a) J. Biomol. NMR., 4, 581–586.

    Google Scholar 

  • Otting, G., Qian, Y.Q., Billeter, M., Müller, M., Affolter, M., Gehring, W.J. and Wüthrich, K. (1990) EMBO J., 9, 3085–3092.

    Google Scholar 

  • Pardi, A., Walker, R., Rapaport, H., Wider, G. and Wüthrich, K. (1983) J. Am. Chem. Soc., 105, 1652–1653.

    Google Scholar 

  • Puglisi, J.D., Chen, L., Blanchard, S. and Frankel, A.D. (1995) Science, 270, 1200–1203.

    Google Scholar 

  • Qian, Y.Q., Otting, G., Billeter, M., Müller, M., Gehring, W. and Wüthrich, K. (1993) J. Mol. Biol., 234, 1070–1083.

    Google Scholar 

  • Santoro, J. and King, G.C. (1992) J. Magn. Reson., 97, 202–207.

    Google Scholar 

  • Shaka, A.J., Barker, P.B. and Freeman, R. (1985) J. Magn. Reson., 64, 547–552.

    Google Scholar 

  • Shaka, A.J., Lee, C.J. and Pines, A.J. (1988) J. Magn. Reson., 77, 274–293.

    Google Scholar 

  • Szyperski, T., Fernández, C. and Wüthrich, K. (1997a) J. Magn. Reson., 128, 228–232.

    Google Scholar 

  • Szyperski, T., Ono, A., Fernández, C., Iwai, H., Tate, S., Wüthrich, K. and Kainosho, M. (1997b) J. Am. Chem. Soc., 119, 9901–9902.

    Google Scholar 

  • Szyperski, T., Fernández, C., Ono, A., Kainosho, M. and Wüthrich, K. (1998) J. Am. Chem. Soc., 120, 821–822.

    Google Scholar 

  • Varani, G., Aboul-ela, F. and Allain, F.H.T. (1996) Prog. NMR Spectrosc., 29, 51–127.

    Google Scholar 

  • Vuister, G.W. and Bax, A. (1992) J. Magn. Reson., 98, 428–435.

    Google Scholar 

  • Wijmenga, S.S., Mooren, M.M.W. and Hilbers, C.W. (1993) In NMR of Macromolecules. A Practical Approach (Ed., Roberts, G.C.K.), Oxford University Press, pp. 217–288.

  • Wishart, D.S., Bigam, C.G., Yao, J., Abildgaard, H.J.D., Markley, J.L. and Sykes, B.D. (1995) J. Biomol. NMR, 6, 135–140.

    Google Scholar 

  • Wüthrich, K. (1986) NMR of Proteins and Nucleic Acids, Wiley, NY.

    Google Scholar 

  • Ye, X., Kumar, R.A. and Patel, D.J. (1995) Chem. Biol., 2, 827–840.

    Google Scholar 

  • Zimmer, D.P. and Crothers, D.M. (1995) Proc. Natl. Acad. Sci. USA, 92, 3091–3095.

    Google Scholar 

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Fernández, C., Szyperski, T., Ono, A. et al. NMR with 13C, 15N-doubly-labeled DNA: The shape Antennapedia homeodomain complex with a 14-mer DNA duplex. J Biomol NMR 12, 25–37 (1998). https://doi.org/10.1023/A:1008280117211

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