Prokaryotic expression, purification and antigenicity identification of mouse prostate stem cell antigen / 南方医科大学学报
Journal of Southern Medical University
;
(12): 502-506, 2012.
Artigo
em Chinês
| WPRIM
| ID: wpr-267567
ABSTRACT
<p><b>OBJECTIVE</b>To amplify mouse prostate stem cell antigen (mPSCA) gene and construct a recombinant plasmid to obtain mPSCA protein and identify its antigenicity.</p><p><b>METHODS</b>The gene of mPSCA was amplified by RT-PCR from mouse prostate cancer cell line RM-1 with the signal peptide sequence removed. The PCR product was cloned into pET-42a prokaryotic expression vector to construct the recombinant plasmid pET-42a-mPSCA, which was transformed into BL21 (DE3) for mPSCA expression. The fusion protein was purified and identified by SDS-PAGE and Western blotting. The antigenicity of the purified protein was characterized by ELISA.</p><p><b>RESULTS</b>The mPSCA gene was obtained with an identical sequence to that retrieved in GenBank. The prokaryotic expression vector for mPSCA was successfully constructed as confirmed by enzyme digestion and DNA sequencing. Both Western blotting and ELISA demonstrated the antigenicity of the purified mPSCA protein.</p><p><b>CONCLUSION</b>The purified mPSCA obtained possesses good antigenicity, which will facilitate further study of immunotherapy for prostate cancer targeting PSCA.</p>
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Plasmídeos
/
Próstata
/
Clonagem Molecular
/
Biologia Celular
/
Alergia e Imunologia
/
Escherichia coli
/
Proteínas Ligadas por GPI
/
Vetores Genéticos
/
Genética
/
Metabolismo
Tipo de estudo:
Estudo diagnóstico
Limite:
Animais
Idioma:
Chinês
Revista:
Journal of Southern Medical University
Ano de publicação:
2012
Tipo de documento:
Artigo
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