| Literature DB >> 35059023 |
Gabriela da Rosa1,2, Leandro Grille1,2, Victoria Calzada3, Katya Ahmad4, Juan Pablo Arcon5, Federica Battistini5, Genís Bayarri5, Thomas Bishop6, Paolo Carloni4, Thomas Cheatham Iii7, Rosana Collepardo-Guevara8, Jacek Czub9, Jorge R Espinosa8, Rodrigo Galindo-Murillo7, Sarah A Harris10, Adam Hospital5, Charles Laughton11, John H Maddocks12, Agnes Noy13, Modesto Orozco5, Marco Pasi14, Alberto Pérez15, Daiva Petkevičiūtė-Gerlach16, Rahul Sharma12, Ran Sun6, Pablo D Dans1,2,5.
Abstract
The structure of B-DNA, the physiological form of the DNA molecule, has been a central topic in biology, chemistry and physics. Far from uniform and rigid, the double helix was revealed as a flexible and structurally polymorphic molecule. Conformational changes that lead to local and global changes in the helix geometry are mediated by a complex choreography of base and backbone rearrangements affecting the ability of the B-DNA to recognize ligands and consequently on its functionality. In this sense, the knowledge obtained from the sequence-dependent structural properties of B-DNA has always been thought crucial to rationalize how ligands and, most notably, proteins recognize B-DNA and modulate its activity, i.e. the structural basis of gene regulation. Honouring the anniversary of the first high-resolution X-ray structure of a B-DNA molecule, in this contribution, we present the most important discoveries of the last 40 years on the sequence-dependent structural and dynamical properties of B-DNA, from the early beginnings to the current frontiers in the field. © International Union for Pure and Applied Biophysics (IUPAB) and Springer-Verlag GmbH Germany, part of Springer Nature 2021.Entities:
Keywords: Ascona B-DNA Consortium; Drew-Dickerson dodecamer; Helical parameters; Nearest neighbours; Structural polymorphisms
Year: 2021 PMID: 35059023 PMCID: PMC8724355 DOI: 10.1007/s12551-021-00893-8
Source DB: PubMed Journal: Biophys Rev ISSN: 1867-2450