Discovery of Antivirals Using Phage Display

被引:19
作者
Sokullu, Esen [1 ,2 ]
Gauthier, Marie-Soleil [1 ]
Coulombe, Benoit [1 ,2 ]
机构
[1] Inst Recherches Clin Montreal, Dept Translat Prote, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Dept Biochem & Mol Med, Montreal, PQ H3C 3J7, Canada
来源
VIRUSES-BASEL | 2021年 / 13卷 / 06期
关键词
phage display; bacteriophage; antiviral; antigen-binding fragment; single-chain variable fragment; nanobody; intrabody; transbody; peptide; RESPIRATORY SYNDROME CORONAVIRUS; SECRETORY TRYPSIN-INHIBITOR; CELL-PENETRATING PEPTIDES; HUMAN MONOCLONAL-ANTIBODY; SINGLE-DOMAIN ANTIBODIES; HEPATITIS-B-VIRUS; CROSS-REACTIVE NEUTRALIZATION; HEAVY-CHAIN ANTIBODIES; IN-VITRO; MIRROR-IMAGE;
D O I
10.3390/v13061120
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The latest coronavirus disease outbreak, COVID-19, has brought attention to viral infections which have posed serious health threats to humankind throughout history. The rapid global spread of COVID-19 is attributed to the increased human mobility of today's world, yet the threat of viral infections to global public health is expected to increase continuously in part due to increasing human-animal interface. Development of antiviral agents is crucial to combat both existing and novel viral infections. Recently, there is a growing interest in peptide/protein-based drug molecules. Antibodies are becoming especially predominant in the drug market. Indeed, in a remarkably short period, four antibody therapeutics were authorized for emergency use in COVID-19 treatment in the US, Russia, and India as of November 2020. Phage display has been one of the most widely used screening methods for peptide/antibody drug discovery. Several phage display-derived biologics are already in the market, and the expiration of intellectual property rights of phage-display antibody discovery platforms suggests an increment in antibody drugs in the near future. This review summarizes the most common phage display libraries used in antiviral discovery, highlights the approaches employed to enhance the antiviral potency of selected peptides/antibody fragments, and finally provides a discussion about the present status of the developed antivirals in clinic.
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页数:26
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