TY - JOUR
T1 - Bullied no more
T2 - When and how DNA shoves proteins around
AU - Fogg, Jonathan M.
AU - Randall, Graham L.
AU - Pettitt, B. Montgomery
AU - Sumners, De Witt L.
AU - Harris, Sarah A.
AU - Zechiedrich, Lynn
PY - 2012/8
Y1 - 2012/8
N2 - The predominant protein-centric perspective in protein-DNA-binding studies assumes that the protein drives the interaction. Research focuses on protein structural motifs, electrostatic surfaces and contact potentials, while DNA is often ignored as a passive polymer to be manipulated. Recent studies of DNA topology, the supercoiling, knotting, and linking of the helices, have shown that DNA has the capability to be an active participant in its transactions. DNA topology-induced structural and geometric changes can drive, or at least strongly influence, the interactions between protein and DNA. Deformations of the B-form structure arise from both the considerable elastic energy arising from supercoiling and from the electrostatic energy. Here, we discuss how these energies are harnessed for topology-driven, sequence-specific deformations that can allow DNA to direct its own metabolism.
AB - The predominant protein-centric perspective in protein-DNA-binding studies assumes that the protein drives the interaction. Research focuses on protein structural motifs, electrostatic surfaces and contact potentials, while DNA is often ignored as a passive polymer to be manipulated. Recent studies of DNA topology, the supercoiling, knotting, and linking of the helices, have shown that DNA has the capability to be an active participant in its transactions. DNA topology-induced structural and geometric changes can drive, or at least strongly influence, the interactions between protein and DNA. Deformations of the B-form structure arise from both the considerable elastic energy arising from supercoiling and from the electrostatic energy. Here, we discuss how these energies are harnessed for topology-driven, sequence-specific deformations that can allow DNA to direct its own metabolism.
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U2 - 10.1017/S0033583512000054
DO - 10.1017/S0033583512000054
M3 - Review article
C2 - 22850561
AN - SCOPUS:84865271294
SN - 0033-5835
VL - 45
SP - 257
EP - 299
JO - Quarterly Reviews of Biophysics
JF - Quarterly Reviews of Biophysics
IS - 3
ER -