TY - JOUR
T1 - Water molecules in DNA recognition I
T2 - Hydration lifetimes of trp operator DNA in solution measured by NMR spectroscopy
AU - Sunnerhagen, Maria
AU - Denisov, Vladimir P.
AU - Venu, Kandadai
AU - Bonvin, Alexandre M.J.J.
AU - Carey, Jannette
AU - Halle, Bertil
AU - Otting, Gottfried
N1 - Funding Information:
Dr T. Lavoie is acknowledged for expert assistance in the preparation of the DNA sample, and Dr H. M. Berman for valuable discussion. This work was supported by NIH grant GM 43558 to J.C., Swedish Natural Science Research Council (NFR) grants to B.H. and G.O., grants from the Magnus Bergwall and Erik and Edith Fernström Foundations to M.S., and NFR postdoctoral fellowships to K.V. and M.S.
PY - 1998/10/2
Y1 - 1998/10/2
N2 - The present NMR study investigates the residence times of the hydration water molecules associated with uncomplexed trp operator DNA in solution by measuring intermolecular nuclear Overhauser effects (NOE) between water and DNA protons, and the nuclear magnetic relaxation dispersion (NMRD) of the water 2H and 17O resonances. Both methods indicate that the hydration water molecules exchange with bulk water on the sub-nanosecond time scale at 4°C. No evidence was obtained for water molecules bound with longer residence times. In particular, the water molecules at the sites of interfacial hydration in the trp repressor/operator complex do not seem kinetically stabilized in the uncomplexed DNA. Analysis of the crystal structures of two different trp repressor/operator complexes shows very similar structural environments for the water molecules mediating specific contacts between the protein and the DNA, whereas much larger variations are observed for the location of corresponding water molecules detected in the crystal structure of an uncomplexed trp operator DNA duplex. Therefore, it appears unlikely that the hydration characteristics of the uncomplexed DNA target would be a major determinant of trp repressor/operator recognition.
AB - The present NMR study investigates the residence times of the hydration water molecules associated with uncomplexed trp operator DNA in solution by measuring intermolecular nuclear Overhauser effects (NOE) between water and DNA protons, and the nuclear magnetic relaxation dispersion (NMRD) of the water 2H and 17O resonances. Both methods indicate that the hydration water molecules exchange with bulk water on the sub-nanosecond time scale at 4°C. No evidence was obtained for water molecules bound with longer residence times. In particular, the water molecules at the sites of interfacial hydration in the trp repressor/operator complex do not seem kinetically stabilized in the uncomplexed DNA. Analysis of the crystal structures of two different trp repressor/operator complexes shows very similar structural environments for the water molecules mediating specific contacts between the protein and the DNA, whereas much larger variations are observed for the location of corresponding water molecules detected in the crystal structure of an uncomplexed trp operator DNA duplex. Therefore, it appears unlikely that the hydration characteristics of the uncomplexed DNA target would be a major determinant of trp repressor/operator recognition.
KW - DNA hydration
KW - NMR spectroscopy
KW - Protein/DNA recognition
KW - trp operator
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U2 - 10.1006/jmbi.1998.2033
DO - 10.1006/jmbi.1998.2033
M3 - Article
C2 - 9743631
AN - SCOPUS:0032475964
SN - 0022-2836
VL - 282
SP - 847
EP - 858
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 4
ER -