TY - JOUR
T1 - Hybrid-hybrid matrix structural refinement of a DNA three-way junction from 3D NOESY-NOESY
AU - Thiviyanathan, Varatharasa
AU - Luxon, Bruce A.
AU - Leontis, Neocles B.
AU - Illangasekare, Nishantha
AU - Donne, David G.
AU - Gorenstein, David G.
N1 - Funding Information:
This work was supported by NIH (AI27744), NIEHS (ES06676), the Welch Foundation (H-1296) and the Sealy and Smith Foundation grants to D.G.G., and NSF CHE-9302619, NIH grants (R01-GM41454 and 1-R15-GM/OD55898-01), ACS-PRF (20871-GB4 and 31427-B4) to N.B.L. Building funds were provided by NIH (1CO6CA59098). The authors thank Mike Hills for helpful discussions.
PY - 1999
Y1 - 1999
N2 - Homonuclear 3D NOESY-NOESY has shown great promise for the structural refinement of large biomolecules. A computationally efficient hybrid-hybrid relaxation matrix refinement methodology, using 3D NOESY-NOESY data, was used to refine the structure of a DNA three-way junction having two unpaired bases at the branch point of the junction. The NMR data and the relaxation matrix refinement confirm that the DNA three-way junction exists in a folded conformation with two of the helical stems stacked upon each other. The third unstacked stem extends away from the junction, forming an acute angle (~60°) with the stacked stems. The two unpaired bases are stacked upon each other and are exposed to the solvent. Helical parameters for the bases in all three strands show slight deviations from typical values expected for right-handed B-form DNA. Inter-nucleotide imino-imino NOEs between the bases at the branch point of the junction show that the junction region is well defined. The helical stems show mobility (± 20°) indicating dynamic processes around the junction region. The unstacked helical stem adjacent to the unpaired bases shows greater mobility compared to the other two stems. The results from this study indicate that the 3D hybrid-hybrid matrix MORASS refinement methodology, by combining the spectral dispersion of 3D NOESY-NOESY and the computational efficiency of 2D refinement programs, provides an accurate and robust means for structure determination of large biomolecules. Our results also indicate that the 3D MORASS method gives higher quality structures compared to the 2D complete relaxation matrix refinement method.
AB - Homonuclear 3D NOESY-NOESY has shown great promise for the structural refinement of large biomolecules. A computationally efficient hybrid-hybrid relaxation matrix refinement methodology, using 3D NOESY-NOESY data, was used to refine the structure of a DNA three-way junction having two unpaired bases at the branch point of the junction. The NMR data and the relaxation matrix refinement confirm that the DNA three-way junction exists in a folded conformation with two of the helical stems stacked upon each other. The third unstacked stem extends away from the junction, forming an acute angle (~60°) with the stacked stems. The two unpaired bases are stacked upon each other and are exposed to the solvent. Helical parameters for the bases in all three strands show slight deviations from typical values expected for right-handed B-form DNA. Inter-nucleotide imino-imino NOEs between the bases at the branch point of the junction show that the junction region is well defined. The helical stems show mobility (± 20°) indicating dynamic processes around the junction region. The unstacked helical stem adjacent to the unpaired bases shows greater mobility compared to the other two stems. The results from this study indicate that the 3D hybrid-hybrid matrix MORASS refinement methodology, by combining the spectral dispersion of 3D NOESY-NOESY and the computational efficiency of 2D refinement programs, provides an accurate and robust means for structure determination of large biomolecules. Our results also indicate that the 3D MORASS method gives higher quality structures compared to the 2D complete relaxation matrix refinement method.
KW - MORASS
KW - NOESY-NOESY
KW - Relaxation matrix analysis
KW - Three-way junction
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U2 - 10.1023/A:1008330011425
DO - 10.1023/A:1008330011425
M3 - Article
C2 - 10481274
AN - SCOPUS:0032819496
SN - 0925-2738
VL - 14
SP - 209
EP - 221
JO - Journal of Biomolecular NMR
JF - Journal of Biomolecular NMR
IS - 3
ER -