DNA
DNA纳米技术
纳米技术
三聚体
DNA折纸
醛缩酶A
化学
材料科学
生物物理学
结晶学
生物
生物化学
二聚体
有机化学
酶
作者
Yang Xu,Shuoxing Jiang,C.R. Simmons,Raghu Pradeep Narayanan,Fei Zhang,Ann Marie Aziz,Hao Yan,Nicholas Stephanopoulos
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-03-05
卷期号:13 (3): 3545-3554
被引量:120
标识
DOI:10.1021/acsnano.8b09798
摘要
Three-dimensional (3D) cages are one of the most important targets for nanotechnology. Both proteins and DNA have been used as building blocks to create tunable nanoscale cages for a wide range of applications, but each molecular type has its own limitations. Here, we report a cage constructed from both protein and DNA building blocks through the use of covalent protein–DNA conjugates. We modified a homotrimeric protein (KDPG aldolase) with three identical single-stranded DNA handles by functionalizing a reactive cysteine residue introduced via site-directed mutagenesis. This protein–DNA building block was coassembled with a triangular DNA structure bearing three complementary arms to the handles, resulting in tetrahedral cages comprising six DNA sides capped by the protein trimer. The dimensions of the cage could be tuned through the number of turns per DNA arm (3 turns ∼ 10 nm, 4 turns ∼ 14 nm), and the hybrid structures were purified and characterized to confirm the three-dimensional structure. Cages were also modified with DNA using click chemistry and using aldolase trimers bearing the noncanonical amino acid 4-azidophenylalanine, demonstrating the generality of the method. Our approach will allow for the construction of nanomaterials that possess the advantages of both protein and DNA nanotechnology and find applications in fields such as targeted delivery, structural biology, biomedicine, and catalytic materials.
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