Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus
Dengue virus (DENV) presents a significant threat to global public health with more than 500,000 hospitalizations and 25,000 deaths annually. Currently, there is no clinically approved antiviral drug to treat DENV infection. The envelope (E) glycoprotein of DENV is a promising target for drug discov...
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doaj-5b7fb191aef247519963b9cedeee8a3d2020-11-25T02:39:34ZengMDPI AGViruses1999-49152020-03-0112436710.3390/v12040367v12040367Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue VirusMohd Ishtiaq Anasir0Babu Ramanathan1Chit Laa Poh2Center for Virus and Vaccine Research, School of Science and Technology, Sunway University, Kuala Lumpur, Selangor 47500, MalaysiaDepartment of Biological Sciences, School of Science and Technology, Sunway University, Kuala Lumpur, Selangor 47500, MalaysiaCenter for Virus and Vaccine Research, School of Science and Technology, Sunway University, Kuala Lumpur, Selangor 47500, MalaysiaDengue virus (DENV) presents a significant threat to global public health with more than 500,000 hospitalizations and 25,000 deaths annually. Currently, there is no clinically approved antiviral drug to treat DENV infection. The envelope (E) glycoprotein of DENV is a promising target for drug discovery as the E protein is important for viral attachment and fusion. Understanding the structure and function of DENV E protein has led to the exploration of structure-based drug discovery of antiviral compounds and peptides against DENV infections. This review summarizes the structural information of the DENV E protein with regards to DENV attachment and fusion. The information enables the development of antiviral agents through structure-based approaches. In addition, this review compares the potency of antivirals targeting the E protein with the antivirals targeting DENV multifunctional enzymes, repurposed drugs and clinically approved antiviral drugs. None of the current DENV antiviral candidates possess potency similar to the approved antiviral drugs which indicates that more efforts and resources must be invested before an effective DENV drug materializes.https://www.mdpi.com/1999-4915/12/4/367dengue virusstructural biologyantiviralenvelope glycoprotein |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohd Ishtiaq Anasir Babu Ramanathan Chit Laa Poh |
spellingShingle |
Mohd Ishtiaq Anasir Babu Ramanathan Chit Laa Poh Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus Viruses dengue virus structural biology antiviral envelope glycoprotein |
author_facet |
Mohd Ishtiaq Anasir Babu Ramanathan Chit Laa Poh |
author_sort |
Mohd Ishtiaq Anasir |
title |
Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus |
title_short |
Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus |
title_full |
Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus |
title_fullStr |
Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus |
title_full_unstemmed |
Structure-Based Design of Antivirals against Envelope Glycoprotein of Dengue Virus |
title_sort |
structure-based design of antivirals against envelope glycoprotein of dengue virus |
publisher |
MDPI AG |
series |
Viruses |
issn |
1999-4915 |
publishDate |
2020-03-01 |
description |
Dengue virus (DENV) presents a significant threat to global public health with more than 500,000 hospitalizations and 25,000 deaths annually. Currently, there is no clinically approved antiviral drug to treat DENV infection. The envelope (E) glycoprotein of DENV is a promising target for drug discovery as the E protein is important for viral attachment and fusion. Understanding the structure and function of DENV E protein has led to the exploration of structure-based drug discovery of antiviral compounds and peptides against DENV infections. This review summarizes the structural information of the DENV E protein with regards to DENV attachment and fusion. The information enables the development of antiviral agents through structure-based approaches. In addition, this review compares the potency of antivirals targeting the E protein with the antivirals targeting DENV multifunctional enzymes, repurposed drugs and clinically approved antiviral drugs. None of the current DENV antiviral candidates possess potency similar to the approved antiviral drugs which indicates that more efforts and resources must be invested before an effective DENV drug materializes. |
topic |
dengue virus structural biology antiviral envelope glycoprotein |
url |
https://www.mdpi.com/1999-4915/12/4/367 |
work_keys_str_mv |
AT mohdishtiaqanasir structurebaseddesignofantiviralsagainstenvelopeglycoproteinofdenguevirus AT baburamanathan structurebaseddesignofantiviralsagainstenvelopeglycoproteinofdenguevirus AT chitlaapoh structurebaseddesignofantiviralsagainstenvelopeglycoproteinofdenguevirus |
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