Translating bioactive peptides for COVID-19 therapy

被引:16
作者
Bhullar, Khushwant S. [1 ,2 ]
Drews, Steven J. [3 ]
Wu, Jianping [1 ]
机构
[1] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2P5, Canada
[2] Univ Alberta, Dept Pharmacol, Edmonton, AB T6G 2P5, Canada
[3] Univ Alberta, Dept Lab Med & Pathol, Canadian Blood Serv, Edmonton, AB T6G 2P5, Canada
关键词
SARS-CoV-2; COVID-19; ACE2; Angiotensin II; Furin; Peptides; ANGIOTENSIN-CONVERTING ENZYME-2; INFLUENZA-VIRUS; SPIKE PROTEIN; SARS-COV; FURIN; INHIBITION; VACCINE; PROPROTEIN; ACTIVATION; EXPRESSION;
D O I
10.1016/j.ejphar.2020.173661
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
COVID-19 (Coronavirus disease 2019) is a global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a positive-sense RNA virus. This virus has emerged as a threat to global health, social stability, and the global economy. This pandemic continues to cause rampant mortality worldwide with the dire urgency to develop novel therapeutic agents. To meet this task, this article discusses advances in the research and potential application of bioactive peptides for possible mitigation of infection by SARS-CoV-2. Growing insight into the molecular biology of SARS-CoV-2 has revealed potential druggable targets for bioactive peptides. Bioactive peptides with unique amino acid sequences can mitigate such targets including, type II transmembrane serine proteases (TMPRSS2) inhibition, furin cleavage, and renin-angiotensin-aldosterone system (RAAS) members. Based on current evidence and structure-function analysis, multiple bioactive peptides present potency to neutralize the virus. To date, no SARS-CoV-2-explicit drug has been reported, but we here introduce bioactive peptides in the perspective of their potential activity against SARS-CoV-2 infection.
引用
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页数:7
相关论文
共 85 条
[1]  
[Anonymous], 2020, LANCET
[2]   A Novel Enediynyl Peptide Inhibitor of Furin That Blocks Processing of proPDGF-A, B and proVEGF-C [J].
Basak, Ajoy ;
Khatib, Abdel-Majid ;
Mohottalage, Dayani ;
Basak, Sarmistha ;
Kolajova, Maria ;
Bag, Subhendu Sekhar ;
Basak, Amit .
PLOS ONE, 2009, 4 (11)
[3]   History about the discovery of the renin-angiotensin system [J].
Basso, N ;
Terragno, NA .
HYPERTENSION, 2001, 38 (06) :1246-1249
[4]   Potent Inhibitors of Furin and Furin-like Proprotein Convertases Containing Decarboxylated P1 Arginine Mimetics [J].
Becker, Gero L. ;
Sielaff, Frank ;
Than, Manuel E. ;
Lindberg, Iris ;
Routhier, Sophie ;
Day, Robert ;
Lu, Yinghui ;
Garten, Wolfgang ;
Steinmetzer, Torsten .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (03) :1067-1075
[5]   TMPRSS2 and TMPRSS4 Facilitate Trypsin-Independent Spread of Influenza Virus in Caco-2 Cells [J].
Bertram, Stephanie ;
Glowacka, Ilona ;
Blazejewska, Paulina ;
Soilleux, Elizabeth ;
Allen, Paul ;
Danisch, Simon ;
Steffen, Imke ;
Choi, So-Young ;
Park, Youngwoo ;
Schneider, Heike ;
Schughart, Klaus ;
Poehlmann, Stefan .
JOURNAL OF VIROLOGY, 2010, 84 (19) :10016-10025
[6]   Antihypertensive peptides of animal origin: A review [J].
Bhat, Zuhaib Fayaz ;
Kumar, Sunil ;
Bhat, Hina Fayaz .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 2017, 57 (03) :566-578
[7]   Angiotensin-converting enzyme 2 - A new cardiac regulator [J].
Boehm, M ;
Nabel, EG .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (22) :1795-1797
[8]   Cleavage of Influenza Virus Hemagglutinin by Airway Proteases TMPRSS2 and HAT Differs in Subcellular Localization and Susceptibility to Protease Inhibitors [J].
Boettcher-Friebertshaeuser, Eva ;
Freuer, Catharina ;
Sielaff, Frank ;
Schmidt, Sarah ;
Eickmann, Markus ;
Uhlendorff, Jennifer ;
Steinmetzer, Torsten ;
Klenk, Hans-Dieter ;
Garten, Wolfgang .
JOURNAL OF VIROLOGY, 2010, 84 (11) :5605-5614
[9]  
Bohm M., 2020, CLIN RES CARDIOL, V1
[10]  
Brosnihan KB, 2003, HYPERTENSION, V42, P749, DOI 10.1161/01.HYP.0000085220.53285.11