NMR characterization of DNA - American Chemical Society

Apr 3, 1984 - Ol1 by Two-DimensionalNOE and /-Correlated. Spectra. Michael A. Weiss,* 1 Dinshaw J. Patel,1 Robert T. Sauer,5 and. Martin Karplus*t...
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J. Am. Chem. SOC.1984, 106, 4269-4270 credence to Winstein’s original s u g g e s t i ~ nthat ’ ~ the saturated parent system, 17, underwent ionization with some anchimeric assistance. Acknowledgment. We are indebted to the National Science Foundation for Grant CHE81-14772, which supported this investigation, and to Dr. W. H. Campbell for his assistance in obtaining high-field N M R data. (14) Gassman, P. G.; Talky, J. J. J. Am. Chem. SOC.1980, 102, 4138. (15) Winstein, S.; Gadient, F.; Stafford, E. T.; Klinedinst, P. E., Jr. J. Am. Chem. SOC. 1958, 80, 5895.

NMR Characterization of DNA: Assignment of Major Groove Sugar Protons of the A-Phage Operator Site 0L1 by Two-Dimensional NOE and J-Correlated Spectra Michael A. Weiss? Dinshaw J. Patel,* Robert T. Sauer,* and Martin Karplus*t Department of Chemistry, Harvard University Cambridge, Massachusetts 021 38 Division of Polymer Science, Bell Laboratories Murray Hill, New Jersey 07974 Department of Biology Massachusetts Institute of Technology Cambridge, Massachusetts 021 39

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s t r a t e g i e ~ ~is- that ~ the DNA double helix, unlike some RNAs (e.g., tRNA) and proteins, is a two-dimensional polymer with a characteristic structure. Protons distant in the primary sequence are also spatially separated, and it is possible to predict which proton N O E s are expected to be n~nnegligible.~Each strand of the B DNA double helix in D 2 0 solution is found to constitute an independent cross-relaxation network of base and sugar protons. Each deoxyribose sugar contributes to this network a distinct set of spins exhibiting strong mutual cross-relaxation, but only weak interaction with the protons of other sugars. Because DNA is a two-dimensional polymer containing a string of largely independent spin reservoirs, spin diffusion can be an aid rather than a hindrance to sequential assignment.lD The H1’ and H2’-”’’ sugar protons and the base protons in the major groove of the OLl DNA double helix have been assigned previously by a sequential meth~d.’.~’*’~ The assignments of these protons can be used to assign the H3’ and H4’ protons. The H3’ protons may be identified by indirect nuclear Overhauser effects ( N O E s ) from the base protons and also from the H1’ and H2’-H2’’ sugar protons. The assignment of these sugar protons to the same sugar is confirmed by a chain of J connectivities from H1’ to H2’ and then from H2’ to H3’ observed in the COSY experiment. The H4’ protons may be identified by NOE’s from the H1’ protons; weak indirect effects are sometimes also observed from the base protons. Where resolved, the J connectivity between the H3’ and H4’ protons verifies the consistency of these two sets of as~ignments.’~ 0,l is an asymmetric duplex of 17 base pairs with sequence

Received October 1 1 , 1983 The 17 base-pair DNA operator site OLl is recognized by the CI and Cro repressors of bacteriophage X and thus provides a model system for specific protein-DNA recognition.’ The solution structure and dynamics of this oligonucleotide are being studied by two-dimensional correlated (COSY) and Overhauser (NOESY) proton N M R method^.^-^ We and others have recently proposed a sequential assignment strategy for oligomers of B DNA.S-S This strategy is extended here to include the major groove sugar protons H3’ and H4’ and is illustrated by the assignment of these protons in the oligonucleotide OLl. The H3’ and H4’ protons are of particular interest because they lie on the outer surface of the double helix and may be involved in ligand binding. The essential element in this and other D N A assignment Harvard University. *Bell Laboratories. Massachusetts Institute of Technology. (1) Johnson, A. D.; Poteete, A. R.; Lauer, G.; Sauer, R. T.; Ackers, G.K.; Ptashne, M. Nature (London)1981, 294, 217. (2) Aue, W. P.; Bartholdi, E.; Ernst, R. R. J. Chem. Phys. 1976,64, 2220. (3) States, D. J.; Haberkorn, R. A,; Ruben, D. J. J. Magn. Reson. 1982, 48, 286. The two-dimensional processing and acquisition software used in these experiments was written by David J. States. (4) Feigon, J.; Wright, J. M.; Leupin, W.; Denny, W. A,; Kearns, D. R. J. Am. Chem. SOC.1982, 104, 5540. ( 5 ) Pardi, A.; Walker, R.; Rapaport, H.; Wider, G.;Wuthrich, K. J. Am. Chem. SOC.1983, 105, 1652. (6) Scheek, R. M.; Russo, N.; Boelens, R.; Kaptein, R.; van Boom, J. M.; J. Am. Chem. SOC.1983, 105, 2914. (7) Weiss, M. A. Patel, D. J.; Sauer, R. T.; Karplus, M. Proc. Narl. Acud. Sci. U.S.A. 1984,81,130. The N O E s identified by this sequential assignment method demonstrate that the l7mer adopts a right-handed B-like structure in solution. This supports the structural assumptions implicit in the H3’-H4’ assignment method presented here. (8) Hare, D. R.; Wemmer, D. E.; Chou, S.-H.; Drobny, G.;Reid, B. R. J. Mol. Biol. 1983, 71, 319. (9) Interproton distances were calculated from hydrogen coordinates inferred from the heavy-atom coordinates given in: Arnott, s.;Cambell-Smith, P.; Chandra Sekharan, P. “CRC Handbook of Biochemistry, of Nucleic Acids”, Chemical Rubber Co.: Cleveland, 1976; Vol. 11, p 41 1. In addition, interproton distances were calculated from the single-crystal B-DNA structures: Dickerson, R. E.; Drew, H. R. J. Mol. Biol. 1981,149,761. Although somewhat different, these distances are consistent with the magnetic model of DNA presented here. The calculations were done with the assistance of Dr. Bernard R. Brooks.

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where for convenience we have numbered the base pairs from left to right; Le., T, is the first (5’) base of the upper strand, A, the last (3’) base of the lower strand. There are eight AT and nine GC base pairs. The variety of magnetic environments makes possible the resolution of many of the individual base and sugar protons. Figure 1 shows a region of the NOESY spectrum containing cross-peaks between thymidine H6 protons and H3’ protons. Each of the thymidine H6 protons in this region cross-relaxes with two H3’ protons: a strong N O E with H3’ of its own sugar and a weaker NOE with that of its 5‘ neighbor.14 Thus, the sequential assignments of the base protons can be extended to assign the H3’ resonances of their sugar. Figure 2 shows a region of the NOESY spectrum containing strong cross-peaks between the H 1’ and H4’ sugar resonances. Since the HI’ resonance at 5.758 ppm has been assigned to T16,7 its cross-relaxation with an H4’ at 4.04 ppm identifies this resonance as H4’ of the same sugar from the distance relations in the B DNA duplex. Cross-peaks a-h are identified similarly, and their assignments are given in the figure caption. Several trends are (10) A major groove base proton, such as a pyrimidine H6, may relax with its own or 5’4anking sugar. The closest neighbor of H6 among its own sugar protons is H2’ (1.94 A in standard B DNA). At short mixing times (