Department of Chemistry and Physiology and Functional Genomics, Shands Cancer Center, University of Florida, Gainesville, Florida 32611-7200, United States.
ACS Nano. 2011 Dec 27;5(12):10090-5. doi: 10.1021/nn204007y. Epub 2011 Nov 28.
Future smart nanostructures will have to rely on molecular assembly for unique or advanced desired functions. For example, the evolved ribosome in nature is one example of functional self-assembly of nucleic acids and proteins employed in nature to perform specific tasks. Artificial self-assembled nanodevices have also been developed to mimic key biofunctions, and various nucleic acid- and protein-based functional nanoassemblies have been reported. However, functionally regulating these nanostructures is still a major challenge. Here we report a general approach to fine-tune the catalytic function of DNA-enzymatic nanosized assemblies by taking advantage of the trans-cis isomerization of azobenzene molecules. To the best of our knowledge, this is the first study to precisely modulate the structures and functions of an enzymatic assembly based on light-induced DNA scaffold switching. Via photocontrolled DNA conformational switching, the proximity of multiple enzyme catalytic centers can be adjusted, as well as the catalytic efficiency of cofactor-mediated DNAzymes. We expect that this approach will lead to the advancement of DNA-enzymatic functional nanostructures in future biomedical and analytical applications.
未来的智能纳米结构将不得不依赖分子组装来实现独特或先进的预期功能。例如,自然界中进化的核糖体就是一种在自然界中用于执行特定任务的核酸和蛋白质功能自组装的例子。人工自组装纳米器件也被开发出来以模拟关键的生物功能,并且已经报道了各种基于核酸和蛋白质的功能性纳米组装。然而,对这些纳米结构进行功能调节仍然是一个主要挑战。在这里,我们报告了一种通过利用偶氮苯分子的顺反异构化来精细调节 DNA-酶纳米级组装的催化功能的通用方法。据我们所知,这是首次基于光诱导 DNA 支架切换来精确调节酶组装结构和功能的研究。通过光控 DNA 构象切换,可以调整多个酶催化中心的接近程度以及辅助因子介导的 DNA 酶的催化效率。我们期望这种方法将推动 DNA-酶功能纳米结构在未来生物医学和分析应用中的发展。