» Articles » PMID: 11893341

Structure of Dengue Virus: Implications for Flavivirus Organization, Maturation, and Fusion

Overview
Journal Cell
Publisher Cell Press
Specialty Cell Biology
Date 2002 Mar 15
PMID 11893341
Citations 695
Authors
Affiliations
Soon will be listed here.
Abstract

The first structure of a flavivirus has been determined by using a combination of cryoelectron microscopy and fitting of the known structure of glycoprotein E into the electron density map. The virus core, within a lipid bilayer, has a less-ordered structure than the external, icosahedral scaffold of 90 glycoprotein E dimers. The three E monomers per icosahedral asymmetric unit do not have quasiequivalent symmetric environments. Difference maps indicate the location of the small membrane protein M relative to the overlaying scaffold of E dimers. The structure suggests that flaviviruses, and by analogy also alphaviruses, employ a fusion mechanism in which the distal beta barrels of domain II of the glycoprotein E are inserted into the cellular membrane.

Citing Articles

Identification and evaluation of bioactive compounds from as potential inhibitors of DENV-2 capsid protein: An integrative study utilizing network pharmacology, molecular docking, molecular dynamics simulations, and machine learning techniques.

Khan M, Zilani M, Hasan M, Hasan N Heliyon. 2025; 11(4):e42594.

PMID: 40051864 PMC: 11883367. DOI: 10.1016/j.heliyon.2025.e42594.


Functional Roles and Host Interactions of Non-Structural Proteins During Replication.

Donaldson M, Zanders L, Jose J Pathogens. 2025; 14(2).

PMID: 40005559 PMC: 11858440. DOI: 10.3390/pathogens14020184.


Utility of VIDAS Dengue Diagnostic Assays to Differentiate Primary and Secondary Dengue Infection: A Cross-Sectional Study in a Military Hospital from Colombia.

Prieto-Torres A, Medina-Lozano L, Ramirez-Avila J, Faccini-Martinez A Trop Med Infect Dis. 2025; 10(2).

PMID: 39998044 PMC: 11860576. DOI: 10.3390/tropicalmed10020040.


Stabilized dengue virus 2 envelope subunit vaccine redirects the neutralizing antibody response to all E-domains.

Thiono D, Samaras D, Phan T, Zhu D, Shah R, Castillo I bioRxiv. 2025; .

PMID: 39990303 PMC: 11844416. DOI: 10.1101/2024.07.18.604114.


Nano-interventions for dengue: a comprehensive review of control, detection and treatment strategies.

Shaikh S, Sandeep Chary P, Mehra N Inflammopharmacology. 2025; .

PMID: 39976669 DOI: 10.1007/s10787-025-01655-8.


References
1.
Allison S, Schalich J, Stiasny K, Mandl C, Kunz C, Heinz F . Oligomeric rearrangement of tick-borne encephalitis virus envelope proteins induced by an acidic pH. J Virol. 1995; 69(2):695-700. PMC: 188630. DOI: 10.1128/JVI.69.2.695-700.1995. View

2.
Forsell K, Xing L, Kozlovska T, Cheng R, Garoff H . Membrane proteins organize a symmetrical virus. EMBO J. 2000; 19(19):5081-91. PMC: 302099. DOI: 10.1093/emboj/19.19.5081. View

3.
Rossmann M . Fitting atomic models into electron-microscopy maps. Acta Crystallogr D Biol Crystallogr. 2000; 56(Pt 10):1341-9. DOI: 10.1107/s0907444900009562. View

4.
Hahn Y, Galler R, Hunkapiller T, Dalrymple J, Strauss J, Strauss E . Nucleotide sequence of dengue 2 RNA and comparison of the encoded proteins with those of other flaviviruses. Virology. 1988; 162(1):167-80. DOI: 10.1016/0042-6822(88)90406-0. View

5.
Corver J, Ortiz A, Allison S, Schalich J, Heinz F, Wilschut J . Membrane fusion activity of tick-borne encephalitis virus and recombinant subviral particles in a liposomal model system. Virology. 2000; 269(1):37-46. DOI: 10.1006/viro.1999.0172. View