Expression of the human prolactin antagonist delta 1-11 G129R-PRL in E. coli periplasm

Carregando...
Imagem de Miniatura
Data
Data de publicação:
2019
Orientador
Título da Revista
ISSN da Revista
Título do Volume
É parte de
É parte de
É parte de
É parte de
BIOPARTITIONING & PURIFICATION CONFERENCE
Exportar
Mendeley
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Recombinant human prolactin antagonist delta 1-11 G129R-hPRL is a 21.9 kDa protein with 188 amino acids that downregulates the proliferation of a variety of cells expressing prolactin receptors. Periplasmic expression of recombinant proteins in E. coli has been considered an option for obtaining an authentic, soluble, and correctly folded protein, as an alternative to the cytoplasmic production in inclusion bodies of an unfolded, insoluble protein, carrying an extra initial methionine. The aim of this work was to carry out the expression of delta 1-11 G129R-hPRL antagonist in the periplasm of E. coli, testing different temperatures. E. coli BL21(DE) strain, transformed with a plasmid based on a pET25b(+) vector, DsbA signal peptide and delta 1-11 G129R-hPRL cDNA, was cultured in LB medium with ampicillin addition. After overnight culture at 30 °C, 0.6 mM IPTG was added and five different temperatures were applied: 25, 30, 32, 35 and 37 °C. Periplasmic fluid was extracted after 5 hours by osmotic shock. The samples were analyzed by SDS-PAGE, Western blotting and RP-HPLC. The best condition was increasing the temperature to 35 °C for 5 h, after having reached the late log phase. The specific expression of 0.14 ± 0.02 μg/mL/A600, with a final optical density of 3.43 ± 0.13 A600 (n = 3) was obtained. Purification by nickel affinity chromatography (Hisprep FF) with Imidazole elution followed by size exclusion chromatography (Sephacryl S-100) was carried out connected to an ÄKTA purification system. Quantification was carried out by comparison between the areas under the curve observed in the HPSEC chromatogram, for the unknown samples versus the Internal Standard of rec-hPRL. The final product showed >95% purity by HPSEC analysis. The delta 1-11 G129R-hPRL antagonist was expressed and purified for further in vivo and in vitro tests, in view of clinical applications for inhibiting cancer cell proliferation that overexpresses prolactin receptor and studies related to prolactin function in anterior pituitary.

Como referenciar
SUZUKI, M.F.; ALMEIDA, L.A.; POMIN, S.A.; SILVA, F.D.; FREIRE, R.P.; OLIVEIRA, J.E.; AFFONSO, R.; BARTOLINI, P.; SOARES, C.R.J. Expression of the human prolactin antagonist delta 1-11 G129R-PRL in E. coli periplasm. In: SANTOS, NATHALIA V. dos (ed.). In: BIOPARTITIONING & PURIFICATION CONFERENCE, November 11-13, 2019, Guarujá, SP. Abstract... São Paulo, SP: Sociedade Brasileira de Microbiologia, 2019. p. 110-110. Disponível em: http://repositorio.ipen.br/handle/123456789/30965. Acesso em: 25 Apr 2024.
Esta referência é gerada automaticamente de acordo com as normas do estilo IPEN/SP (ABNT NBR 6023) e recomenda-se uma verificação final e ajustes caso necessário.

Agência de fomento