Research Center for Advanced Science and Technology, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8904, Japan.
J Am Chem Soc. 2010 Jul 28;132(29):9937-9. doi: 10.1021/ja104702q.
Desired enzyme nanoarrays patterned on a DNA origami scaffold were selectively isolated by affinity tag purification from a pool of differently patterned nanoarrays, and their enzymatic activity was successfully confirmed. As few as 12 histidine residues were enough to hold a huge complex of DNA origami with multiple proteins, 260 nm in length and 5.2 MDa in molecular weight, to an immobilized metal affinity resin.
在 DNA 折纸支架上设计所需的酶纳米阵列,通过亲和标签从不同图案的纳米阵列混合物中选择性地分离出来,并成功确认了它们的酶活性。仅需 12 个组氨酸残基即可将长度为 260nm 且分子量为 5.2MDa 的具有多个蛋白质的大型 DNA 折纸复合物固定在固定化金属亲和树脂上。