DNA-Based Synthetic Growth Factor Surrogates with Fine-Tuned Agonism**

被引:21
作者
Akiyama, Momoko [1 ]
Ueki, Ryosuke [1 ]
Yanagawa, Masataka [2 ]
Abe, Mitsuhiro [2 ]
Hiroshima, Michio [2 ,3 ]
Sako, Yasushi [2 ]
Sando, Shinsuke [1 ,4 ]
机构
[1] Univ Tokyo, Dept Chem & Biotechnol, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[2] RIKEN Cluster Pioneering Res, Cellular Informat Lab, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[3] RIKEN Ctr Biosyst Dynam Res, Lab Cell Signaling Dynam, 6-2-3 Furuedai, Suita, Osaka 5650874, Japan
[4] Univ Tokyo, Dept Bioengn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
aptamers; growth factors; receptors; signal transduction; MET; CYTOKINE; APTAMERS; ANTIBODIES; RECEPTORS; HGF;
D O I
10.1002/anie.202105314
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Designing synthetic surrogates of functional proteins is an important, albeit challenging, task in the field of chemistry. A strategy toward the design of synthetic agonists for growth factor or cytokine receptors that elicit a desired signal activity has been in high demand, as such ligands hold great promise as safer and more effective therapeutics. In the present study, we used a DNA aptamer as a building block and described the strategy-guided design of a synthetic receptor agonist with fine-tuned agonism. The developed synthetic partial agonist can regulate therapeutically relevant cellular activities by eliciting fine-tuned receptor signaling.
引用
收藏
页码:22745 / 22752
页数:8
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