4.2 Article

Two-step purification of tag-free norovirus-like particles from silkworm larvae (Bombyx mori)

期刊

PROTEIN EXPRESSION AND PURIFICATION
卷 190, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pep.2021.106010

关键词

Norovirus; Virus-like particle; Silkworm; Purification

资金

  1. Japan Society for the Promotion of Science (JSPS) KAKENHI [20H00411]
  2. Grants-in-Aid for Scientific Research [20H00411] Funding Source: KAKEN

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This study successfully expressed recombinant VP1 of norovirus in silkworms, resulting in the formation of highly purified NoV-LPs. The purified VLPs were shown to be structurally correct, biologically functional, and exhibited potential applications in a vaccine platform. Furthermore, the silkworm-based expression system is known for its robustness, scalability, and cost-effectiveness compared to insect cell systems.
Recombinantly expressed VP1 of norovirus self-assembled and formed norovirus-like particles (NoV-LPs). This native VP1 was expressed using the Bombyx mori nucleopolyhedrovirus (BmNPV) expression system in silkworm larva. NoV-LPs were collected from silkworm fat body lysate by density gradient centrifugation. To improve the purity of the NoV-LP, the proteins were further purified using immobilized metal affinity chromatography based on the surface exposed side chain of histidine residues. The additional purification led to a highly purified viruslike particle (VLP). The morphology and size of the purified VLPs were examined using a transmission electron microscope, and dynamic light scattering revealed a monodispersed spherical morphology with a diameter of 34 nm. The purified product had a purity of >90% with a recovery yield of 48.7% (equivalent to 930 mu g) from crude lysate, obtained from seven silkworm larvae. In addition, the purified VLP could be recognized by antibodies against GII norovirus in sandwich enzyme-linked immunosorbent assay, which indicated that the silkwormderived VLP is biologically functional as a NoV-LP in its native state, is structurally correct, and exerts its biological function. Our results suggest that the silkworm-derived NoV-LP may be useful for subsequent applications, such as in a vaccine platform. Moreover, the silkworm-based expression system is known for its robustness, facile up-scalability, and relatively low expense compared to insect cell systems.

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