Wang Shiyu, Saneyoshi Hisao, Xu Pengyu, Oguri Nobuyuki, Yamashita Atsushi, Xu Yan
Division of Chemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan.
SynCrest Inc., 2Chome26-1, Muraokahigashi, Fujisawa, Kanagawa 251-0012, Japan.
Nucleic Acids Res. 2025 Jun 20;53(12). doi: 10.1093/nar/gkaf571.
Effectively controlling the structures of DNA and RNA is crucial for their functional utilization in material development, biological regulation, and medical applications. Here, we present a gain-of-function strategy for controlling DNA and RNA structures using an inverse electron-demand Diels-Alder (IEDDA) based click-to-release reaction. By incorporating click reaction-cleavable caged moiety into oligonucleotides, we disrupt activated base pairs, allowing controlled release of biofunctional higher-order nucleic acid structures. This click-to-release caged DNA was employed to control DNA duplex formation. Next, we demonstrated the utility of "click-to-release" strategy for regulated release of Z-DNA or Z-RNA and bind associated proteins. In addition, the approach was used to manipulated G-quadruplex formation in vitro and in vivo, enabling visual detection of G-quadruplex using BVE-caged DNA with fluorescent dye. Furthermore, we demonstrated the utility of click-to-release caged DNA for Quantum Dots (QDs) functionalization, enabling precise molecular imaging for cancer diagnosis. Finally, we developed a click-to-release controllable nucleic acid aptamer for precise blood clotting regulation and anticoagulation therapy. This strategy provides moderate kinetics, excellent orthogonality, and biocompatibility. It establishes a new pathway towards control of nucleic acid structures and functions, which has promising applications in various biological procedures and nucleic acid medicines.
有效控制DNA和RNA的结构对于它们在材料开发、生物调节和医学应用中的功能利用至关重要。在此,我们提出一种基于逆电子需求狄尔斯-阿尔德(IEDDA)点击释放反应来控制DNA和RNA结构的功能获得策略。通过将点击反应可裂解的笼蔽部分引入寡核苷酸中,我们破坏了活化的碱基对,从而实现生物功能高阶核酸结构的可控释放。这种点击释放笼蔽DNA被用于控制DNA双链体的形成。接下来,我们展示了“点击释放”策略在Z-DNA或Z-RNA的调控释放以及结合相关蛋白方面的效用。此外,该方法被用于在体外和体内操纵G-四链体的形成,使用带有荧光染料的BVE笼蔽DNA能够实现G-四链体的可视化检测。此外,我们证明了点击释放笼蔽DNA用于量子点(QD)功能化的效用,能够实现用于癌症诊断的精确分子成像。最后,我们开发了一种用于精确凝血调节和抗凝治疗的点击释放可控核酸适配体。该策略具有适度的动力学、出色的正交性和生物相容性。它为控制核酸结构和功能建立了一条新途径,在各种生物过程和核酸药物中具有广阔的应用前景。
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