Recent Progress in Site-Selective Modification of Peptides and Proteins Using Macrocycles

被引:1
|
作者
Wang, Ye-Cheng [1 ,2 ]
Bai, Si-Cong [3 ]
Ye, Wei-Lin [1 ,2 ]
Jiang, Jing [1 ]
Li, Gao [1 ,4 ]
机构
[1] Minjiang Univ, Fuzhou Inst Oceanog, Coll Mat & Chem Engn, Fuzhou 350108, Fujian, Peoples R China
[2] Fuzhou Univ, Coll Chem Engn, Fuzhou 350108, Fujian, Peoples R China
[3] Fujian Agr & Forestry Univ, Sch Future Technol, Fuzhou 350002, Fujian, Peoples R China
[4] Minjiang Univ, Fujian Taiwan Hongkong Macao Sci & Technol Coopera, Fuzhou 350108, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
AQUEOUS-SOLUTION; RECOGNITION; CYCLOADDITION; CUCURBITURIL; STABILITY; CYSTEINE;
D O I
10.1021/acs.bioconjchem.3c00534
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Peptides and proteins undergo crucial modifications to alter their physicochemical properties to expand their applications in diverse fields. Various techniques, such as unnatural amino acid incorporation, enzyme catalysis, and chemoselective methods, have been employed for site-selective peptide and protein modification. While traditional methods remain valuable, advancement in host-guest chemistry introduces innovative and promising approaches for the selective modification of peptides and proteins. Macrocycles exhibit robust binding affinities, particularly with natural amino acids, which facilitates their use in selectively binding to specific sequences. This distinctive property endows macrocycles with the potential for modification of target peptides and proteins. This review provides a comprehensive overview of strategies utilizing macrocycles for the selective modification of peptides and proteins. These strategies unlock new possibilities for constructing antibody-drug conjugates and stabilizing volatile medications.
引用
收藏
页码:277 / 285
页数:9
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