Department of Physical Chemistry, Fritz Haber Institute of the Max Planck Society, Berlin, Germany.
PLoS One. 2011;6(7):e21809. doi: 10.1371/journal.pone.0021809. Epub 2011 Jul 19.
Helicases are motor proteins that play a central role in the metabolism of DNA and RNA in biological cells. Using the energy of ATP molecules, they are able to translocate along the nucleic acids and unwind their duplex structure. They have been extensively characterized in the past and grouped into superfamilies based on structural similarities and sequential motifs. However, their functional aspects and the mechanism of their operation are not yet well understood. Here, we consider three helicases from the major superfamily 2--Hef, Hel308 and XPD--and study their conformational dynamics by using coarse-grained relaxational elastic network models. Specifically, their responses to mechanical perturbations are analyzed. This enables us to identify robust and ordered conformational motions which may underlie the functional activity of these proteins. As we show, such motions are well-organized and have large amplitudes. Their possible roles in the processing of nucleic substrate are discussed.
解旋酶是一类在生物细胞中参与 DNA 和 RNA 代谢的重要的马达蛋白。它们利用 ATP 分子的能量沿着核酸分子运动并解开其双链结构。过去,人们对解旋酶进行了广泛的研究,并根据结构相似性和序列基序将其分为超家族。然而,它们的功能方面和作用机制尚未得到很好的理解。在这里,我们研究了来自主要超家族 2 的三种解旋酶——Hef、Hel308 和 XPD,并通过使用粗粒化松弛弹性网络模型来研究它们的构象动力学。具体来说,我们分析了它们对机械扰动的响应。这使我们能够识别可能是这些蛋白质功能活性基础的稳健有序的构象运动。正如我们所展示的,这些运动组织有序且幅度较大。我们还讨论了它们在核酸底物加工中的可能作用。