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Related Concept Videos

Inhibitors of Viral Protein Synthesis01:30

Inhibitors of Viral Protein Synthesis

Protein synthesis is indispensable for viral replication, as viruses lack the cellular machinery required for this process and must hijack the host's translational apparatus. In response, host cells deploy a critical innate immune defense involving interferons, specialized cytokines that play a central role in inhibiting viral propagation.Upon viral detection, infected cells release interferons that bind to receptors on adjacent uninfected cells, activating the JAK-STAT signaling pathway and...
Inhibitors Of Virion Release01:25

Inhibitors Of Virion Release

Viral replication and dissemination rely on efficient mechanisms for host cell entry, genome replication, assembly, and release. Influenza viruses, such as types A and B, are negative-sense single-stranded RNA viruses with a segmented genome, that depend on two critical surface glycoproteins to carry out these processes: hemagglutinin (HA) and neuraminidase (NA). HA initiates infection by binding to sialic acid residues on the surface of host epithelial cells, facilitating receptor-mediated...
Inhibitors of Virion Maturation and Assembly01:19

Inhibitors of Virion Maturation and Assembly

As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...

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Related Experiment Video

Updated: Jun 18, 2026

Zika Virus Specific Diagnostic Epitope Discovery
11:37

Zika Virus Specific Diagnostic Epitope Discovery

Published on: December 12, 2017

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Envelope Protein-Targeting Zika Virus Entry Inhibitors.

Abhijeet Roy1, Qian Liu1, Yang Yang2

  • 1Institute for Biomedical Sciences, Georgia State University, Atlanta, GA 30303, USA.

International Journal of Molecular Sciences
|September 14, 2024
PubMed
Summary
This summary is machine-generated.

Zika virus (ZIKV) entry inhibitors targeting the E protein are crucial for combating severe diseases like congenital Zika syndrome. This review guides the development of potent and safe ZIKV entry inhibitors.

Keywords:
Zika virusentry inhibitorsenvelop proteinflavivirusstructural proteins

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Area of Science:

  • Virology
  • Infectious Diseases
  • Drug Discovery

Background:

  • Zika virus (ZIKV) causes severe neurological conditions, including congenital Zika syndrome and Guillain-Barré Syndrome.
  • While primarily mosquito-borne, ZIKV transmission occurs through other routes, necessitating broad-spectrum countermeasures.
  • The ZIKV envelope (E) protein is vital for viral entry and pathogenesis, representing a prime target for therapeutic intervention.

Purpose of the Study:

  • To review the life cycle, genome, and proteins of ZIKV.
  • To illustrate the structure and function of the ZIKV E protein.
  • To summarize ZIKV E protein-targeting entry inhibitors and discuss development challenges.

Main Methods:

  • Literature review of ZIKV biology and E protein structure-function.
  • Analysis of existing entry inhibitors, focusing on natural products and small molecules.
  • Identification of challenges in developing ZIKV entry inhibitors.

Main Results:

  • The ZIKV E protein's critical role in viral entry and pathogenesis is detailed.
  • Various E protein-targeting entry inhibitors, including those from natural products and small molecules, are summarized.
  • Key challenges hindering the development of effective ZIKV inhibitors are highlighted.

Conclusions:

  • Targeting the ZIKV E protein is a promising strategy for developing effective entry inhibitors.
  • Further research is needed to overcome challenges and develop safe and potent ZIKV inhibitors.
  • This review provides guidance for future development of ZIKV entry inhibitors.