Author:
Khetarpal Niyati,Poddar Ankur,Nemani Satish K,Dhar Nisha,Patil Aravind,Negi Priyanka,Perween Ashiya,Viswanathan Ramaswamy,Lünsdorf Heinrich,Tyagi Poornima,Raut Rajendra,Arora Upasana,Jain Swatantra K,Rinas Ursula,Swaminathan Sathyamangalam,Khanna Navin
Abstract
Abstract
Background
Dengue is today the most significant of arboviral diseases. Novel tools are necessary to effectively address the problem of dengue. Virus-like particles (VLP) offer a versatile nanoscale platform for developing tools with potential biomedical applications. From the perspective of a potentially useful dengue-specific tool, the dengue virus envelope protein domain III (EDIII), endowed with serotype-specificity, host receptor recognition and the capacity to elicit virus-neutralizing antibodies, is an attractive candidate.
Methods
We have developed a strategy to co-express and co-purify Hepatitis B virus surface (S) antigen in two forms: independently and as a fusion with EDIII. We characterized these physically and functionally.
Results
The two forms of the S antigen associate into VLPs. The ability of these to display EDIII in a functionally accessible manner is dependent upon the relative levels of the two forms of the S antigen. Mosaic VLPs containing the fused and un-fused components in 1:4 ratio displayed maximal functional competence.
Conclusions
VLPs armed with EDIII may be potentially useful in diagnostic, therapeutic and prophylactic applications.
Publisher
Springer Science and Business Media LLC
Subject
Pharmaceutical Science,Applied Microbiology and Biotechnology,Biomedical Engineering,Molecular Medicine,Medicine (miscellaneous),Bioengineering
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