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Appl Microbiol Biotechnol ; 62(5-6): 478-83, 2003 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-12750854

RESUMO

Biotinylated thermo-responsive magnetic nanoparticles for use in affinity selection from yeast cell surface display libraries were prepared by coating magnetite nanoparticles with a thermo-responsive polymer consisting of N-isopropyl acrylamide and a biotin derivative. These particles showed a reversible transition between flocculation and dispersion at around the lower critical solution temperature of 30 degrees C, above which the flocculated particles--which absorbed a large amount of avidin due to their large surface area--were quickly separable by magnet. The model library was constructed by mixing control yeast cells with target yeast cells co-displaying IgG binding protein (ZZ) and enhanced green fluorescence protein. Biotinylated IgG and avidin were subsequently added to the model library, and target cells were efficiently enriched with the biotinylated magnetic nanoparticles by avidin-biotin sandwich and ZZ-IgG interaction. The few target cells (0.001%) in the model library were enriched by up to 100% in only 5 days by an affinity selection procedure repeated four times. This novel method based on magnetic nanoparticles and a yeast cell surface display system could fulfill a wide range of applications in the analysis of protein-protein interactions and rapid isolation of novel biomolecules.


Assuntos
Membrana Celular/metabolismo , Separação Imunomagnética/métodos , Proteínas/metabolismo , Proteínas Recombinantes de Fusão/metabolismo , Saccharomyces cerevisiae/metabolismo , Avidina/metabolismo , Proteínas de Bactérias/genética , Proteínas de Bactérias/metabolismo , Biotinilação , Membrana Celular/genética , Floculação , Proteínas de Fluorescência Verde , Fragmentos Fc das Imunoglobulinas/metabolismo , Proteínas Luminescentes/genética , Proteínas Luminescentes/metabolismo , Lectinas de Ligação a Manose , Microesferas , Nanotecnologia , Biblioteca de Peptídeos , Proteínas/química , Proteínas/isolamento & purificação , Proteínas Recombinantes de Fusão/biossíntese , Proteínas Recombinantes de Fusão/química , Proteínas Recombinantes de Fusão/isolamento & purificação , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/isolamento & purificação , Proteínas de Saccharomyces cerevisiae/genética , Proteínas de Saccharomyces cerevisiae/metabolismo , Suspensões , Temperatura
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