Nuclear Overhauser effect-derived distances between adenine H2 protons and anomeric Hi' protons on the same strand or on the complementary strand are presented for several different DNA duplexes. The cross-strand (n)AH2 to (m + 1)Hl' distances [designated as x, where (u) and (m) are complementary residues] vary by up to 1 A depending on the sequence. In all possible A-containing pyrimidine-purine steps (CA, TG, and TA), x is >4.5 A. In GA steps, x varies within rather wide limits in the range 3.8-4.5 A, whereas in AA steps the lower limit is 3.7 A and the upper limit is ==4.2 A. In purine-purine steps, x is affected by at least three factors: (i) adjacent pyrimidine-purine steps at the 5' end [e.g., YRA sequences (where Y = T or C and R = G or A)], or a pyrimidine-purine step at the 3' end of the pyrimidinepyrimidine step on the complementary strand, cause x to increase, (fi) an AT step at the 3' end of a purine-purine step (e.g., RAT) causes x to decrease, and (ii) substitution of bases at the next-nearest neighbor position leads to changes in x at GA and AA steps. The latter factor seems to be due to a cooperative effect arising from formation of the "anomalous" B' structure when the substitution produces an A.T1, tract (which always produces a decrease in x). The data indicate that (n)AH2-(n + 1)Hl' distances on the same strand (designated as s) are also sequence dependent. Thus on AA steps, neighboring substitutions produce the same effect on s as on the cross-strand x distances. The results lead to the ability to predt changes in AH2-H1' distances depending on the DNA sequence. By using high-resolution x-ray B-type structures as a set of allowable B conformations, a very good correlation was found between x and the minor groove width parameters P-P or Hl'-Hl'. Thus, the x distances are a direct probe of the minor groove width in B-type DNA, and changes in this distance therefore reflect changes in the minor groove width. Since many of the sequences studied are sites of protein recognition, the observed sequence-structure dependence in DNA probably plays an important role in the process of recognition by proteins and minor groove ligands such as drugs.Determination of the sequence dependence of the DNA double helix structure is a subject that has attracted attention for several years. Considerable progress has been achieved lately in this area, particularly in DNA sequences containing A/T tracts (1, 2), but many problems remain. Neither x-ray structure analysis nor NMR has been entirely successful in attempts to solve this problem so far. The approach based on single-crystal x-ray structure analysis has been compromised by two problems: first, relatively few DNA sequences have been crystallized and solved to high resolution in the B-form (3, 4), and second, crystal packing forces have been shown to affect the structure (5, 6). Even if a reliable relationship between B-DNA conformation and sequence could be determined in the crystalline state, it remains unclear whether this relationship would hold in...