1H, 13C, and 15N resonance assignments and secondary structure analysis of the HU protein from Bacillus stearothermophilus using two- and three-dimensional double- and triple-resonance heteronuclear magnetic resonance spectroscopy

Nearly complete 1H, 13C, and 15N resonance assignments have been obtained for the protein HU from Bacillus stearothermophilus (dimer, 19.5 kDa) using double- and triple-resonance 2D and 3D NMR experiments. This has resulted in assignments of 91% of the observable protons, 98% of all 13C, and 92% of all 15N nuclei. NOEs obtained from a 3D time-shared NOESY- (13C,15N)-HSQC spectrum, exchange data of amide protons, and chemical shifts of the 1H(α), 1H(N), 13C(β), 13C(α), 13CO, and 15N nuclei have been used to identify the secondary structure elements. Three α- helices (residues 3-13, 18-37, and 83-90) and three extended strands (residues 40-45, 48-62, and 67-82) have been found in HU. The arrangement of these elements of secondary structure is very similar to the X-ray structure [Tanaka et al. (1984) Nature 310, 376-381; White et al. (1989) Proteins 5, 281-288]. The conformation of the proposed DNA-binding region of HU, i.e., an antiparallel β-hairpin, was not observed previously in the X-ray structure. In the NMR structure long range NOEs in the β-arm region (residues 53-76) suggest a distortion between residue Pro-72 and Ala-73 and between Pro-63 and Gln-64 with concomitant distortions in the opposite strand. The NOE data indicate further that the loop region in the DNA-binding arms of HU is arranged as a type I β-turn from Pro-63 to Gly-66.