Broad-Spectrum Antiviral Peptides and Polymers

被引:26
作者
Kuroki, Agnes [1 ,2 ]
Tay, Joyce [2 ]
Lee, Guan Huei [1 ]
Yang, Yi Yan [2 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore 117597, Singapore
[2] Inst Bioengn & Bioimaging, 31 Biopolis Ways, Singapore 138669, Singapore
基金
英国医学研究理事会;
关键词
antiviral mechanisms; antivirals; chemical structures; peptides; polymers; HERPES-SIMPLEX-VIRUS; NUCLEIC-ACID POLYMERS; HYDROPHOBIC POLYCATIONIC COATINGS; FUCOIDAN-MIMETIC GLYCOPOLYMERS; SULFATE-BINDING PEPTIDE; IN-VITRO; HEPARAN-SULFATE; INFLUENZA-VIRUS; MEMBRANE-FUSION; HEPATITIS-B;
D O I
10.1002/adhm.202101113
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
As the human cost of the pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is still being witnessed worldwide, the development of broad-spectrum antiviral agents against emerging and re-emerging viruses is seen as a necessity to hamper the spread of infections. Various targets during the viral life-cycle can be considered to inhibit viral infection, from viral attachment to viral fusion or replication. Macromolecules represent a particularly attractive class of therapeutics due to their multivalency and versatility. Although several antiviral macromolecules hold great promise in clinical applications, the emergence of resistance after prolonged exposure urges the need for improved solutions. In the present article, the recent advancement in the discovery of antiviral peptides and polymers with diverse structural features and antiviral mechanisms is reviewed. Future perspectives, such as, the development of virucidal peptides/polymers and their coatings against SARS-CoV-2 infection, standardization of antiviral testing protocols, and use of artificial intelligence or machine learning as a tool to accelerate the discovery of antiviral macromolecules, are discussed.
引用
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页数:27
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