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Biophys J, April 2000, p. 1988-1996, Vol. 78, No. 4
and
*Laboratori de Medicina Computacional, Unitat de
Bioestadística, Facultat de Medicina, Universitat
Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain;
Facultad de Ciencias, Universidad Autónoma del Edo.
de Morelos, 62210 Cuernavaca, Morelos, México; and
Department of Physiology and Biophysics, Mount Sinai
School of Medicine, New York, New York 10029 USA
One of the common mechanisms of DNA bending by minor
groove-binding proteins is the insertion of protein side chains between basepair steps, exemplified in TBP (TATA box-binding protein)/DNA complexes. At the central basepair step of the TATA box TBP produces a
noticeable decrease in twist and an increase in
roll, while engaging in hydrogen bonds with the bases
and sugars. This suggests a mechanism for the stabilization of DNA
kinks that was explored here with ab initio quantum mechanical
calculations and molecular dynamics/potential of mean force
calculations. The hydrogen bonds are found to contribute the energy
necessary to drive the conformational transition at the central
basepair step. The Asn, Thr, and Gly residues involved in hydrogen
bonding to the DNA bases and sugar oxygens form a relatively rigid
motif in TBP. The interaction of this motif with DNA is found to be
responsible for inducing the untwisting and
rolling of the central basepair step. Notably, direct
readout is shown not to be capable of discriminating between AA and AT
steps, as the strength of the hydrogen bonds between TBP and the DNA
are the same for both sequences. Rather, the calculated free energy
cost for an equivalent conformational transition is found to be
sequence-dependent, and is calculated to be higher for AA steps than
for AT steps.
Biophys J, April 2000, p. 1988-1996, Vol. 78, No. 4
© 2000 by the Biophysical Society 0006-3495/00/04/1988/09 $2.00
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