MERS-CoV spike protein: a key target for antivirals. (1st February 2017)
- Record Type:
- Journal Article
- Title:
- MERS-CoV spike protein: a key target for antivirals. (1st February 2017)
- Main Title:
- MERS-CoV spike protein: a key target for antivirals
- Authors:
- Du, Lanying
Yang, Yang
Zhou, Yusen
Lu, Lu
Li, Fang
Jiang, Shibo - Abstract:
- ABSTRACT: Introduction: The continual Middle East respiratory syndrome (MERS) threat highlights the importance of developing effective antiviral therapeutics to prevent and treat MERS coronavirus (MERS-CoV) infection. A surface spike (S) protein guides MERS-CoV entry into host cells by binding to cellular receptor dipeptidyl peptidase-4 (DPP4), followed by fusion between virus and host cell membranes. MERS-CoV S protein represents a key target for developing therapeutics to block viral entry and inhibit membrane fusion. Areas covered: This review illustrates MERS-CoV S protein's structure and function, particularly S1 receptor-binding domain (RBD) and S2 heptad repeat 1 (HR1) as therapeutic targets, and summarizes current advancement on developing anti-MERS-CoV therapeutics, focusing on neutralizing monoclonal antibodies (mAbs) and antiviral peptides. Expert opinion: No anti-MERS-CoV therapeutic is approved for human use. Several S-targeting neutralizing mAbs and peptides have demonstrated efficacy against MERS-CoV infection, providing feasibility for development. Generally, human neutralizing mAbs targeting RBD are more potent than those targeting other regions of S protein. However, emergence of escape mutant viruses and mAb's limitations make it necessary for combining neutralizing mAbs recognizing different neutralizing epitopes and engineering them with improved efficacy and reduced cost. Optimization of the peptide sequences is expected to produce next-generationABSTRACT: Introduction: The continual Middle East respiratory syndrome (MERS) threat highlights the importance of developing effective antiviral therapeutics to prevent and treat MERS coronavirus (MERS-CoV) infection. A surface spike (S) protein guides MERS-CoV entry into host cells by binding to cellular receptor dipeptidyl peptidase-4 (DPP4), followed by fusion between virus and host cell membranes. MERS-CoV S protein represents a key target for developing therapeutics to block viral entry and inhibit membrane fusion. Areas covered: This review illustrates MERS-CoV S protein's structure and function, particularly S1 receptor-binding domain (RBD) and S2 heptad repeat 1 (HR1) as therapeutic targets, and summarizes current advancement on developing anti-MERS-CoV therapeutics, focusing on neutralizing monoclonal antibodies (mAbs) and antiviral peptides. Expert opinion: No anti-MERS-CoV therapeutic is approved for human use. Several S-targeting neutralizing mAbs and peptides have demonstrated efficacy against MERS-CoV infection, providing feasibility for development. Generally, human neutralizing mAbs targeting RBD are more potent than those targeting other regions of S protein. However, emergence of escape mutant viruses and mAb's limitations make it necessary for combining neutralizing mAbs recognizing different neutralizing epitopes and engineering them with improved efficacy and reduced cost. Optimization of the peptide sequences is expected to produce next-generation anti-MERS-CoV peptides with improved potency. … (more)
- Is Part Of:
- Expert opinion on therapeutic targets. Volume 21:Number 2(2017:Feb.)
- Journal:
- Expert opinion on therapeutic targets
- Issue:
- Volume 21:Number 2(2017:Feb.)
- Issue Display:
- Volume 21, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 21
- Issue:
- 2
- Issue Sort Value:
- 2017-0021-0002-0000
- Page Start:
- 131
- Page End:
- 143
- Publication Date:
- 2017-02-01
- Subjects:
- MERS -- MERS-CoV -- spike protein -- receptor-binding domain -- membrane fusion -- monoclonal antibodies -- peptides -- therapeutics
Drugs -- Research -- Periodicals
615.072 - Journal URLs:
- http://informahealthcare.com/journal/ett ↗
http://informahealthcare.com ↗
http://juno.ashley-pub.com/vl=2061206/cl=65/nw=1/rpsv/journal/journal8_home.htm ↗ - DOI:
- 10.1080/14728222.2017.1271415 ↗
- Languages:
- English
- ISSNs:
- 1744-7631
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002965
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 290.xml