氢键
配对
碱基对
蛋白质设计
DNA
模块化设计
蛋白质结构
蛋白质工程
化学
纳米技术
计算生物学
生物
材料科学
物理
分子
计算机科学
酶
生物化学
程序设计语言
量子力学
有机化学
超导电性
作者
Scott E. Boyken,Zibo Chen,Benjamin Groves,Robert A. Langan,Gustav Oberdorfer,Alex Ford,Jason M. Gilmore,Chunfu Xu,Frank DiMaio,J.H. Pereira,Banumathi Sankaran,Georg Seelig,Peter H. Zwart,David Baker
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2016-05-06
卷期号:352 (6286): 680-687
被引量:306
标识
DOI:10.1126/science.aad8865
摘要
Building with designed proteins General design principles for protein interaction specificity are challenging to extract. DNA nanotechnology, on the other hand, has harnessed the limited set of hydrogen-bonding interactions from Watson-Crick base-pairing to design and build a wide range of shapes. Protein-based materials have the potential for even greater geometric and chemical diversity, including additional functionality. Boyken et al. designed a class of protein oligomers that have interaction specificity determined by modular arrays of extensive hydrogen bond networks (see the Perspective by Netzer and Fleishman). They use the approach, which could one day become programmable, to build novel topologies with two concentric rings of helices. Science , this issue p. 680 ; see also p. 657
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