转导(生物物理学)
纳米技术
核酸
寡核苷酸
DNA
合成生物学
计算机科学
材料科学
化学
生物物理学
计算生物学
生物
生物化学
作者
Dan Bai,Jianhong Zhang,Yaoyi Zhang,Hongyan Yu,Li Zhang,Xiaole Han,Ke Lv,Li Wang,Wang Luo,You Wu,Xi Zhou,Weitao Wang,Tong Feng,Guoming Xie
出处
期刊:Small
[Wiley]
日期:2023-12-10
卷期号:20 (18)
被引量:7
标识
DOI:10.1002/smll.202307421
摘要
Abstract DNA strand displacement reactions are vital for constructing intricate nucleic acid circuits, owing to their programmability and predictability. However, the scarcity of effective methods for eliminating circuit leakages has hampered the construction of circuits with increased complexity. Herein, a versatile strategy is developed that relies on a spatially controlled proximity split tweezer (PST) switch to transduce the biomolecular signals into the independent oligonucleotides. Leveraging the double‐stranded rigidity of the tweezer works synergistically with the hindering effect of the hairpin lock, effectively minimizing circuit leakage compared with sequence‐level methods. In addition, the freely designed output strand is independent of the target binding sequence, allowing the PST switch conformation to be modulated by nucleic acids, small molecules, and proteins, exhibiting remarkable adaptability to a wide range of targets. Using this platform, established logical operations between different types of targets for multifunctional transduction are successfully established. Most importantly, the platform can be directly coupled with DNA catalytic circuits to further enhance transduction performance. The uniqueness of this platform lies in its design straightforwardness, flexibility, scalable intricacy, and system compatibility. These attributes pave a broad path toward nucleic acid‐based development of sophisticated transduction networks, making them widely applied in basic science research and biomedical applications.
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