scholarly journals Enhanced Prokaryotic Expression of Dengue Virus Envelope Protein

2013 ◽  
Vol 16 (4) ◽  
pp. 609 ◽  
Author(s):  
Advaita Ganguly ◽  
Ravindra B. Malabadi ◽  
Dipankar Das ◽  
Mavanur R. Suresh ◽  
Hoon H Sunwoo

Purpose. To highlight the expression and purification of the recombinant dengue virus type-1 antigen exploiting the codon optimized full length envelope for increased yield in E. coli. Methods. A 6x His tag was inserted at the C terminus to facilitate purification. The purified protein was recognized in Western blot by Monoclonal antibody specific for the tag. The in vitro refolded recombinant protein was used to immunize mice for the development of hybridomas and also analyzed for its biological functionality with heparan sulfate binding assay. Results. The polyclonal anti-sera from the immunized mice were found to recognize the envelope protein thereby establishing the immunogenicity of the protein. Conclusion. The purified envelope protein could potentially be used towards dengue diagnostics and vaccine development efforts. This article is open to POST-PUBLICATION REVIEW. Registered readers (see “For Readers”) may comment by clicking on ABSTRACT on the issue’s contents page.

2021 ◽  
Vol 12 ◽  
Author(s):  
Te-Sheng Lien ◽  
Der-Shan Sun ◽  
Shih-Che Hung ◽  
Wen-Sheng Wu ◽  
Hsin-Hou Chang

Abnormal immune responses and cytokine storm are involved in the development of severe dengue, a life-threatening disease with high mortality. Dengue virus-induced neutrophil NETosis response is associated with cytokine storm; while the role of viral factors on the elicitation of excessive inflammation mains unclear. Here we found that treatments of dengue virus envelope protein domain III (EIII), cellular binding moiety of virion, is sufficient to induce neutrophil NETosis processes in vitro and in vivo. Challenges of EIII in inflammasome Nlrp3−/− and Casp1−/− mutant mice resulted in less inflammation and NETosis responses, as compared to the wild type controls. Blockages of EIII-neutrophil interaction using cell-binding competitive inhibitor or selective Nlrp3 inflammasome inhibitors OLT1177 and Z-WHED-FMK can suppress EIII-induced NETosis response. These results collectively suggest that Nlrp3 inflammsome is a molecular target for treating dengue-elicited inflammatory pathogenesis.


2019 ◽  
Vol 17 (7) ◽  
pp. 1408-1417 ◽  
Author(s):  
André Eerde ◽  
Johanna Gottschamel ◽  
Ralph Bock ◽  
Kristine Eraker Aasland Hansen ◽  
Hetron Mweemba Munang'andu ◽  
...  

2017 ◽  
Vol 71 ◽  
pp. 152-160 ◽  
Author(s):  
Abdul Wadood ◽  
Aamir Mehmood ◽  
Huma Khan ◽  
Muhammad Ilyas ◽  
Ayaz Ahmad ◽  
...  

2020 ◽  
Vol 278 ◽  
pp. 197882
Author(s):  
Yongchao Zhou ◽  
Dong Chen ◽  
Lan Yang ◽  
Weiwei Zou ◽  
Zhiliang Duan ◽  
...  

2010 ◽  
Vol 150 ◽  
pp. 484-484
Author(s):  
C. Martinez ◽  
A.M Giulietti ◽  
J. Rodriguez Talou ◽  
H. Mason

2001 ◽  
Vol 44 (13) ◽  
pp. 2178-2187 ◽  
Author(s):  
Rory M. Marks ◽  
Hong Lu ◽  
Renuka Sundaresan ◽  
Toshihiko Toida ◽  
Atsushi Suzuki ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document