Travers A A
MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK.
Philos Trans A Math Phys Eng Sci. 2004 Jul 15;362(1820):1423-38. doi: 10.1098/rsta.2004.1390.
Although the average physico-chemical properties of a long DNA molecule may approximate to those of a thin isotropic homogeneous rod, DNA behaves more locally as an anisotropic heterogeneous rod. This bending anisotropy is sequence dependent and to a first approximation reflects both the geometry and stability of individual base steps. The biological manipulation and packaging of the molecule often depend crucially on local variations in both bending and torsional flexibility. However, whereas the probability of DNA untwisting can be strongly correlated with a high bending flexibility, DNA bending, especially when the molecule is tightly wrapped on a protein surface, may be energetically favoured by a less flexible sequence whose preferred configuration conforms more closely to that of the complementary protein surface. In the latter situation the lower bending flexibility may be more than compensated for on binding by a reduced required deformation energy relative to a fully isotropic DNA molecule.
尽管长DNA分子的平均物理化学性质可能近似于细的各向同性均匀棒的性质,但DNA在局部表现得更像是各向异性的异质棒。这种弯曲各向异性取决于序列,并且在一阶近似下反映了单个碱基步的几何形状和稳定性。分子的生物操作和包装通常关键取决于弯曲和扭转灵活性的局部变化。然而,虽然DNA解旋的概率可能与高弯曲灵活性密切相关,但DNA弯曲,特别是当分子紧密包裹在蛋白质表面时,可能在能量上更倾向于具有较低灵活性的序列,其优选构型更紧密地符合互补蛋白质表面的构型。在后一种情况下,相对于完全各向同性的DNA分子,较低的弯曲灵活性可能通过结合时所需变形能的降低而得到更多补偿。