Expression and characterization of HPV-16 L1 capsid protein in Pichia pastoris

Autor: Karina Araújo Aires, Robert L. Garcea, Silvia B. Bazan, Paulo Lee Ho, Agtha de Alencar Muniz Chaves, Aurora Marques Cianciarullo
Rok vydání: 2009
Předmět:
Zdroj: Archives of Virology. 154:1609-1617
ISSN: 1432-8798
0304-8608
DOI: 10.1007/s00705-009-0484-8
Popis: Human papillomaviruses (HPVs) are responsible for the most common human sexually transmitted viral infections. Infection with high-risk HPVs, particularly HPV16, is associated with the development of cervical cancer. The papillomavirus L1 major capsid protein, the basis of the currently marketed vaccines, self-assembles into virus-like particles (VLPs). Here, we describe the expression, purification and characterization of recombinant HPV16 L1 produced by a methylotrophic yeast. A codon-optimized HPV16 L1 gene was cloned into a non-integrative expression vector under the regulation of a methanol-inducible promoter and used to transform competent Pichia pastoris cells. Purification of L1 protein from yeast extracts was performed using heparin–sepharose chromatography, followed by a disassembly/reassembly step. VLPs could be assembled from the purified L1 protein, as demonstrated by electron microscopy. The display of conformational epitopes on the VLPs surface was confirmed by hemagglutination and hemagglutination inhibition assays and by immuno-electron microscopy. This study has implications for the development of an alternative platform for the production of a papillomavirus vaccine that could be provided by public health programs, especially in resource-poor areas, where there is a great demand for low-cost vaccines.
Databáze: OpenAIRE
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