Department of Biochemistry, Duke University School of Medicine, Durham, NC 27710, USA.
Center for Genomic and Computational Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Curr Opin Struct Biol. 2024 Dec;89:102949. doi: 10.1016/j.sbi.2024.102949. Epub 2024 Nov 9.
The energy cost accompanying changes in the structures of nucleic acids when they bind partner molecules is a significant but underappreciated thermodynamic contribution to binding affinity and specificity. This review highlights recent advances in measuring conformational penalties and determining their contribution to the recognition, folding, and regulatory activities of nucleic acids. Notable progress includes methods for measuring and structurally characterizing lowly populated conformational states, obtaining ensemble information in high throughput, for large macromolecular assemblies, and in complex cellular environments. Additionally, quantitative and predictive thermodynamic models have been developed that relate conformational penalties to nucleic acid-protein association and cellular activity. These studies underscore the crucial role of conformational penalties in nucleic acid recognition.
当核酸与其配对分子结合时,其结构发生变化所伴随的能量消耗是对结合亲和力和特异性具有重要意义但尚未得到充分认识的热力学贡献。本综述强调了最近在测量构象惩罚并确定其对核酸识别、折叠和调节活性的贡献方面的进展。值得注意的进展包括用于测量和结构表征低 populate 构象状态的方法,以及在高通量、大的大分子组装体和复杂的细胞环境中获得整体信息的方法。此外,还开发了定量和预测热力学模型,将构象惩罚与核酸-蛋白质相互作用和细胞活性联系起来。这些研究强调了构象惩罚在核酸识别中的关键作用。