DNA motions consist of several components which couple, making their i
nvestigation difficult. This study describes an approach for obtaining
dynamical information by EPR when spin-labeled nucleic acids are exam
ined. The analysis is accomplished by implementing two motional models
. The first model (i.e., dynamic cylinder model) views the spin-labele
d helix as a diffusing cylinder containing internal dynamics which are
characterized by an order parameter. The second model (i.e., base dis
k model) provides correlation times describing the diffusion of the sp
in-labeled base. In each model, the nitroxide motion consists of both
global and internal contributions. Dynamic cylinder and base disk simu
lations of four duplexes containing nitroxides attached to thymidine b
y a two-atom tether (DUMTA)-(dT)(7)DUMTA-(dT)(7) .(dA>(15), [(dT)7DUMT
A(dT)(7)](2) .(dA)(30), [(dT)(7)DUMTA(dT)(7)](3) .(dA)(45), and [(dT)(
7)DUMTk(dT)(7)](m) .-(dA)(n)-demonstrate the useful application of thi
s approach. From dynamic cylinder simulations, the order parameter for
internal motions is found to be independent of the helix length (S =
0.32 +/- 0.01). Previous base disk simulations of a DNA 26mer and poly
mer labeled with a five-atom-tethered nitroxide seemed to indicate tha
t tau(perpendicular to) was only sensitive to internal dynamics. Resul
ts from base disk simulations of DUMTA-labeled DNA indicate that the p
erpendicular component of the base disk correlation time (tau(perpendi
cular to) 1.4-6.2 ns) is sensitive to global dynamics. Thus, tau(perpe
ndicular to) is a quantitative indicator of both internal and global d
ynamics, Comparison of the two models reveals that tau(perpendicular t
o) proportional to S-2 tau(rb), where tau(rb) represents the rigid-bod
y diffusion of the DNA helix. This relationship between S and tau(perp
endicular to) provides a framework for studying conformational changes
and size-dependent phenomena in spin-labeled nucleic acids. Applicati
on of the dynamic cylinder model to a B-Z transition generates distinc
t values of S for each of the conformations, indicating that Z-DNA is
more rigid than B-DNA.