MINOR-GROOVE HYDRATION OF DNA IN SOLUTION - DEPENDENCE ON BASE COMPOSITION AND SEQUENCE

Citation
H. Johannesson et B. Halle, MINOR-GROOVE HYDRATION OF DNA IN SOLUTION - DEPENDENCE ON BASE COMPOSITION AND SEQUENCE, Journal of the American Chemical Society, 120(28), 1998, pp. 6859-6870
Citations number
85
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
120
Issue
28
Year of publication
1998
Pages
6859 - 6870
Database
ISI
SICI code
0002-7863(1998)120:28<6859:MHODIS>2.0.ZU;2-J
Abstract
The hydration of six B-DNA dodecamers with A-tracts of variable length and sequence has been investigated via the nuclear magnetic relaxatio n dispersion (NMRD) of the water H-2 and O-17 resonances. By subdividi ng the aqueous DNA solution into microscopic emulsion droplets, NMRD m easurements could be performed at -20 degrees C, thereby greatly enhan cing the sensitivity of the method. The NMRD profiles show that all si x dodecamers contain long-lived water molecules. These water molecules are displaced by netropsin and must therefore be located in the minor groove. The number of long-lived water molecules is correlated with t he width of the minor groove as seen in crystal structures. The NMRD d ata are consistent with a single file of 3-9 long-lived water molecule s located at the base pair steps and extending 1-2 steps on either sid e of the A-tract. Dodecamers with central A-tracts of sequence A(4)T(4 ), T(4)A(4), and (AT)(4) are found to contain seven or nine long-lived water molecules, challenging the common view that T-A steps widen the minor groove and disrupt the hydration structure. The long-lived wate r molecules observed here are highly ordered with an entropy comparabl e to that of water molecules in ice, but most of them undergo a symmet ric flip motion while residing in the groove. The mean water residence time is essentially the same, 10-15 ns at -20 degrees C, for all inve stigated dodecamers, suggesting that water exchange occurs from an ope n state with a uniformly wide minor groove. From the temperature depen dence of the water residence time, an activation enthalpy of 53 kJ mol (-1) is obtained for this process.