Chow Dominic C, Lee Woo-Kyung, Zauscher Stefan, Chilkoti Ashutosh
Department of Biomedical Engineering, Duke University, Box 90281, Durham, NC 27708-0281, USA.
J Am Chem Soc. 2005 Oct 19;127(41):14122-3. doi: 10.1021/ja052491z.
Nucleic acid nanostructures are useful as templates for bionanofabrication of composite molecular nanostructures in materials science, molecular electronics, and biosensing. Here, we demonstrate that terminal deoxynucleotidyl transferase, which repetitively adds mononucleotides to the 3' end of a short DNA initiator, can be used to rapidly fabricate DNA nanostructures up to 121 nm high with lateral dimensions from 0.1 to 4 mum in 2 h. These programmable scaffolds can potentially be employed to build more complex nanostructures consisting of natural or unnatural nucleotides with selective docking sites along the single-stranded DNA.
核酸纳米结构在材料科学、分子电子学和生物传感领域作为复合分子纳米结构生物制造的模板很有用。在此,我们证明了末端脱氧核苷酸转移酶,它能将单核苷酸重复添加到短DNA起始物的3'末端,可用于在2小时内快速制造高度达121纳米、横向尺寸从0.1到4微米的DNA纳米结构。这些可编程支架有可能用于构建由天然或非天然核苷酸组成的更复杂纳米结构,沿着单链DNA具有选择性对接位点。