Site-specific incorporation of reduction-controlled guest amino acids into proteins for cucurbituril recognition

被引:2
|
作者
Dai, Zhen [1 ,2 ]
Tan, Linzhi [2 ]
Su, Yeyu [2 ]
Zhao, Kerui [2 ]
Tian, Yushun [2 ]
Liu, Yu [1 ]
Liu, Tao [2 ]
机构
[1] Nankai Univ, Coll Chem, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, Dept Mol & Cellular Pharmacol, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
基金
北京市自然科学基金;
关键词
Protein recognition; Host-guest recognition; Non-canonical amino acids; Staudinger reduction; Expanded genetic code; GENETIC-CODE; CONSTRUCTION;
D O I
10.1016/j.cclet.2023.109121
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Protein recognition using host-guest recognition approach is of great interest but has been limited mainly to the protein N-terminal residues. Here, we site-specific incorporated two novel non-canonical amino acids containing supramolecular guest motifs into protein via an expanded genetic code. Through Staudinger reduction reactions, the encoded unnatural residues on protein becoming activated and can be specifically recognized by cucurbit[7]uril (CB[7]) and cucurbit[8]uril (CB[8]). We demonstrated that enzyme containing guest amino acid incorporated near the active site can be reversibly regulated by CB[7] recognition, and CB[8] recognition induces protein dimerization. These amino acids will make useful addition to the supramolecular toolbox for protein targeting using molecular recognition approaches. (c) 2024 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页数:4
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