模块化设计
感应(电子)
计算机科学
计算生物学
接口(物质)
透视图(图形)
蛋白质设计
配体(生物化学)
纳米技术
化学
生物
蛋白质结构
人工智能
生物化学
受体
程序设计语言
材料科学
肺表面活性物质
吉布斯等温线
物理化学
作者
Anum Glasgow,Yao-Ming Huang,Daniel J. Mandell,Michael C. Thompson,Ryan Ritterson,Amanda L. Loshbaugh,J. Pellegrino,Cody Krivacic,Roland A. Pache,Kyle A. Barlow,Noah Ollikainen,Deborah Jeon,Mark J. S. Kelly,James S. Fraser,Tanja Kortemme
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-11-22
卷期号:366 (6468): 1024-1028
被引量:108
标识
DOI:10.1126/science.aax8780
摘要
Sense and respond Many signaling pathways start with cellular proteins sensing and responding to small molecules. Despite advances in protein design, creating a protein-based sense-and-respond system remains challenging. Glasgow et al. designed binding sites at the interface of protein heterodimers (see the Perspective by Chica). By fusing each monomer to one half of a split reporter, they linked ligand-driven dimerization to the reporter output. The computational design strategy provides a generalizable approach to create synthetic sensing systems with different outputs. Science , this issue p. 1024 ; see also p. 952
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