Reprogramming natural proteins using unnatural amino acids

被引:50
作者
Adhikari, Anup [1 ]
Bhattarai, Bibek Raj [1 ]
Aryal, Ashika [2 ]
Thapa, Niru [1 ]
Puja, K. C. [1 ]
Adhikari, Ashma [1 ]
Maharjan, Sushila [1 ]
Chanda, Prem B. [3 ]
Regmi, Bishnu P. [4 ]
Parajuli, Niranjan [1 ]
机构
[1] Tribhuvan Univ, Cent Dept Chem, Biol Chem Lab, Kathmandu 44618, Nepal
[2] Tribhuvan Univ, Dept Chem, Birendra Multiple Campus, Bharatpur, Chitwan, Nepal
[3] Southeastern Louisiana Univ, Dept Chem & Phys, Hammond, LA 70402 USA
[4] Florida A&M Univ, Dept Chem, Tallahassee, FL 32307 USA
关键词
GENETIC-CODE EXPANSION; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; F-18-FLUCICLOVINE PET/CT; BIOCATALYTIC PRODUCTION; GLOBAL INCORPORATION; REDUCTIVE AMINATION; TARGETED DELIVERY; L-THREONINE; SITE;
D O I
10.1039/d1ra07028b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Unnatural amino acids have gained significant attention in protein engineering and drug discovery as they allow the evolution of proteins with enhanced stability and activity. The incorporation of unnatural amino acids into proteins offers a rational approach to engineer enzymes for designing efficient biocatalysts that exhibit versatile physicochemical properties and biological functions. This review highlights the biological and synthetic routes of unnatural amino acids to yield a modified protein with altered functionality and their incorporation methods. Unnatural amino acids offer a wide array of applications such as antibody-drug conjugates, probes for change in protein conformation and structure-activity relationships, peptide-based imaging, antimicrobial activities, etc. Besides their emerging applications in fundamental and applied science, systemic research is necessary to explore unnatural amino acids with novel side chains that can address the limitations of natural amino acids.
引用
收藏
页码:38126 / 38145
页数:20
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