Ultrashort Peptides for the Self-Assembly of an Antiviral Coating

被引:8
|
作者
Hu, Tan [1 ,2 ,3 ,4 ]
Kaganovich, Michaela [1 ,2 ]
Shpilt, Zohar [1 ,2 ]
Pramanik, Apurba [1 ,2 ]
Agazani, Omer [1 ,2 ]
Pan, Siyi [3 ,4 ]
Tshuva, Edit [1 ,2 ]
Reches, Meital [1 ,2 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Ctr Nanosci & Nanotechnol, IL-91904 Jerusalem, Israel
[3] Huazhong Agr Univ, Coll Food Sci & Technol, Wuhan 430070, Hubei, Peoples R China
[4] Huazhong Agr Univ, Key Lab Environm Correlat Dietol, Minist Educ, Wuhan 430070, Hubei, Peoples R China
关键词
antiviral; bacteriophage T4; nanoparticles; peptides; self-assembly; INFLUENZA-VIRUS; INACTIVATION; PROTEIN; FLUORINE;
D O I
10.1002/admi.202202161
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Antiviral compounds are important for generating sterile surfaces. Here, two extremely short peptides, DOPA-Phe-NH2 and DOPA-Phe(4F)-NH2 that can self-assemble into spherical nanoparticles with antiviral activity are presented. The peptide assemblies possess excellent antiviral activity against bacteriophage T4 with antiviral minimal inhibitory concentrations of 125 and 62.5 mu g mL(-1), for DOPA-Phe-NH2 and DOPA-Phe(4F)-NH2, respectively. When the peptide assemblies are applied on a glass substrate by drop-casting, they deactivate more than 99.9% of bacteriophage T4 and Canine coronavirus. Importantly, the peptide assemblies have low toxicity toward mammalian cells. Overall, the findings can provide a novel strategy for the design and development of antiviral coatings for a decreased risk of viral infections.
引用
收藏
页数:8
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