Stratingh Institute for Chemistry , University of Groningen , Nijenborgh 4 , 9747 AG Groningen , The Netherlands.
Zernike Institute for Advanced Materials , University of Groningen , Nijenborgh 4 , 9747AG Groningen , The Netherlands.
J Am Chem Soc. 2018 Apr 18;140(15):5069-5076. doi: 10.1021/jacs.7b09476. Epub 2018 Apr 10.
Reversible control over the functionality of biological systems via external triggers may be used in future medicine to reduce the need for invasive procedures. Additionally, externally regulated biomacromolecules are now considered as particularly attractive tools in nanoscience and the design of smart materials, due to their highly programmable nature and complex functionality. Incorporation of photoswitches into biomolecules, such as peptides, antibiotics, and nucleic acids, has generated exciting results in the past few years. Molecular motors offer the potential for new and more precise methods of photoregulation, due to their multistate switching cycle, unidirectionality of rotation, and helicity inversion during the rotational steps. Aided by computational studies, we designed and synthesized a photoswitchable DNA hairpin, in which a molecular motor serves as the bridgehead unit. After it was determined that motor function was not affected by the rigid arms of the linker, solid-phase synthesis was employed to incorporate the motor into an 8-base-pair self-complementary DNA strand. With the photoswitchable bridgehead in place, hairpin formation was unimpaired, while the motor part of this advanced biohybrid system retains excellent photochemical properties. Rotation of the motor generates large changes in structure, and as a consequence the duplex stability of the oligonucleotide could be regulated by UV light irradiation. Additionally, Molecular Dynamics computations were employed to rationalize the observed behavior of the motor-DNA hybrid. The results presented herein establish molecular motors as powerful multistate switches for application in biological environments.
通过外部触发对生物系统功能进行可逆控制,未来可能在医学中用于减少对有创程序的需求。此外,由于其高度可编程性和复杂功能,外部调节的生物大分子现在被认为是纳米科学和智能材料设计中特别有吸引力的工具。在过去几年中,将光开关整合到生物分子(如肽、抗生素和核酸)中已经取得了令人兴奋的结果。由于分子马达具有多态切换循环、旋转的单向性以及在旋转步骤中螺旋反转的特性,因此为新的、更精确的光调节方法提供了潜力。在计算研究的辅助下,我们设计并合成了一种光可切换的 DNA 发夹,其中分子马达作为桥接单元。在确定链接器的刚性臂不会影响马达功能之后,采用固相合成将马达整合到 8 个碱基对的自我互补 DNA 链中。有了可光切换的桥接单元,发夹形成不受影响,而这个高级生物杂交系统的马达部分保留了出色的光化学性质。马达的旋转会产生结构的巨大变化,因此通过紫外线照射可以调节寡核苷酸的双链稳定性。此外,还采用分子动力学计算来合理化观察到的马达-DNA 杂交体的行为。本文提出的结果确立了分子马达作为在生物环境中应用的强大多态开关。