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Construction of a phage antibody library and screening of anti-epidermal growth factor receptor variant III single chain antibody / 南方医科大学学报
Journal of Southern Medical University ; (12): 25-29, 2010.
Artículo en Chino | WPRIM | ID: wpr-269635
ABSTRACT
<p><b>OBJECTIVE</b>To obtain specific anti-epidermal growth factor receptor variant III (EGFRvIII) single chain antibody (ScFv) by phage antibody library display system.</p><p><b>METHODS</b>The total RNA was extracted from the spleen B cells of BALB/c mice immunized with pep-3-OVA protein, and the first-strand cDNA was synthesized by reverse transcription. Antibody VH and VL gene fragments were amplified and joined to a ScFv gene with the linker. The ScFv gene was ligated into the phagemid vector pCANTAB5E, which was transformed into competent E. coli TG1. The transformed cells were then infected with M13KO7 helper phage to yield the recombinant phage to construct the phage ScFv library. Pep-3-BSA protein was used to screen the phage antibody library and ELISA carried out to characterize the activity of the antibody.</p><p><b>RESULTS</b>The VH and VL gene fragments of the antibody were about 350 bp and 320 bp in length as analyzed by agarose gel electrophoresis. The ScFv gene was 780 bp, consistent with the expected length. The recombinant phagemid with ScFv gene insert was rescued, and an immune phage ScFv library with the content of 5.0x10(6) was constructed. The recombinant ScFv phage had a titer of 3.0x10(4) cfu/ml, and the fourth phage harvest yielded 56 times as much as that of the first one. SDS-PAGE demonstrated a molecular mass of the soluble ScFv of about 28 kD. ELISA results indicated good specificity of the ScFv to bind EGFRvIII.</p><p><b>CONCLUSION</b>An immune phage ScFv library is successfully constructed, and the ScFv antibody fragment is capable of specific binding to EGFRvIII.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fragmentos de Inmunoglobulinas / Datos de Secuencia Molecular / Secuencia de Bases / Secuencia de Aminoácidos / Cadenas Pesadas de Inmunoglobulina / Cadenas Ligeras de Inmunoglobulina / Biblioteca de Péptidos / Alergia e Inmunología / Proteínas Mutantes / Anticuerpos de Cadena Única Tipo de estudio: Estudio diagnóstico / Estudio de tamizaje Límite: Animales Idioma: Chino Revista: Journal of Southern Medical University Año: 2010 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fragmentos de Inmunoglobulinas / Datos de Secuencia Molecular / Secuencia de Bases / Secuencia de Aminoácidos / Cadenas Pesadas de Inmunoglobulina / Cadenas Ligeras de Inmunoglobulina / Biblioteca de Péptidos / Alergia e Inmunología / Proteínas Mutantes / Anticuerpos de Cadena Única Tipo de estudio: Estudio diagnóstico / Estudio de tamizaje Límite: Animales Idioma: Chino Revista: Journal of Southern Medical University Año: 2010 Tipo del documento: Artículo