Your browser doesn't support javascript.
loading
Production of dengue virus-like particles serotype-3 in silkworm larvae and their ability to elicit a humoral immune response in mice.
Utomo, Doddy Irawan Setyo; Pambudi, Sabar; Sjatha, Fithriyah; Kato, Tatsuya; Park, Enoch Y.
Afiliação
  • Utomo DIS; Laboratory of Biotechnology, Graduate School of Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
  • Pambudi S; Center of Pharmaceutical and Medical Technology, Agency for the Assessment and Application of Technology (BPPT), Jl. Kawasan Puspiptek, Gedung I LAPTIAB, Kota Tangerang Selatan, Banten, 15314, Indonesia.
  • Sjatha F; Department of Microbiology, Faculty of Medicine, Universitas Indonesia, Jl.Pegangsaan Timur 16, Cikini, Jakarta, 10320, Indonesia.
  • Kato T; Laboratory of Biotechnology, Graduate School of Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
  • Park EY; Laboratory of Biotechnology, Research Institute of Green Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529, Japan.
AMB Express ; 10(1): 147, 2020 Aug 17.
Article em En | MEDLINE | ID: mdl-32804287
To develop monovalent dengue virus-like particle for serotype 3 (DENV-LP/3), we prepared and expressed two structural polyprotein constructs using silkworm and Bm5 cells: DENV-3 Capsid-premembrane-envelope (DENV-3CprME) and premembrane-envelope (DENV-3prME). The expressed PA-tagged 3CprME and 3prME polypeptides were partially purified by PA-tag affinity chromatography and had molecular weights of 85 and 75 kDa, respectively. Expressed proteins were separately verified using the following primary antibodies: the anti-PA tag antibody, DENV premembrane polyclonal antibody, and DENV envelope polyclonal antibody. Transmission electron microscopy revealed that these DENV-3CprME and 3prME formed rough, spherical DENV-LPs (DENV-LP/3CprME and DENV-LP/3prME), respectively, with a diameter of 30-55 nm. The heparin-binding assay demonstrated that these DENV-LPs contained the envelope protein domain III on their surfaces. Both DENV-LPs showed an affinity to sera from human dengue patients and immunized mice. Immunization of mice with DENV-LP/3prME significantly induced the level of antibodies compared with DENV-LP/3CprME. These results indicate that DENV-LP/3prME is suitable as a vaccine candidate compared with DENV-LP/3CprME.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: AMB Express Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: AMB Express Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão