HOW AMINO-ACIDS CONTROL THE BINDING OF CU(II) IONS TO DNA .1. THE ROLE OF THE HYDROXYL GROUP OF SERINE AND THREONINE IN FIXING THE ORIENTATION OF THE COMPLEXES
W. Harada et al., HOW AMINO-ACIDS CONTROL THE BINDING OF CU(II) IONS TO DNA .1. THE ROLE OF THE HYDROXYL GROUP OF SERINE AND THREONINE IN FIXING THE ORIENTATION OF THE COMPLEXES, Journal of inorganic biochemistry, 64(4), 1996, pp. 273-285
ESR data have been obtained on some hydrated copper(II) and copper(II)
amino acid complexes bound to highly oriented DNA fibers. The complex
es bind with random orientation on A-form DNA, while some of them bind
stereospecifically on B-form DNA. The hydrated copper(II) ions bind t
o at least two different sites on B-form DNA at room temperature; one
site is so mobile that the orientations of the complex fluctuate dynam
ically, while the other site fixes the orientation of the bound ions s
uch that the angle between the g(parallel to) axis and the DNA helical
axes becomes ca. 55 degrees. The g(parallel to) axis of glycine compl
ex on B-form DNA at room temperature is aligned parallel to the fiber
axis with large fluctuations in the orientation. L-serine and L-threon
ine fix the g(parallel to) axes of some of the complexes parallel to t
he fiber axes, indicating that the hydroxyl groups work as linkers to
bind the complexes stereospecifically to B-form DNA. The hydroxyl grou
ps in D-isomers do not work as L-isomers. (C) 1996 Elsevier Science In
c.