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Protein Expr Purif ; 67(2): 139-47, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19457455

RESUMO

Peptide libraries have proven to be useful in applications such as substrate profiling, drug candidate screening and identifying protein-protein interaction partners. However, issues of fidelity, peptide length, and purity have been encountered when peptide libraries are chemically synthesized. Biochemically produced libraries, on the other hand, circumvent many of these issues due to the fidelity of the protein synthesis machinery. Using thioredoxin as an expression partner, a stably folded peptide scaffold (avian pancreatic polypeptide) and a compatible cleavage site for human rhinovirus 3C protease, we report a method that allows robust expression of a genetically encoded peptide library, which yields peptides of high purity. In addition, we report the use of methodological synchronization, an experimental design created for the production of a library, from initial cloning to peptide characterization, within a 5-week period of time. Total peptide yields ranged from 0.8% to 16%, which corresponds to 2-70 mg of pure peptide. Additionally, no correlation was observed between the ability to be expressed or overall yield of peptide-fusions and the intrinsic chemical characteristics of the peptides, indicating that this system can be used for a wide variety of peptide sequences with a range of chemical characteristics.


Assuntos
Biblioteca de Peptídeos , Peptídeos/metabolismo , Engenharia de Proteínas/métodos , Proteínas Recombinantes de Fusão/metabolismo , Proteases Virais 3C , Sequência de Aminoácidos , Cromatografia Líquida de Alta Pressão , Clonagem Molecular , Cisteína Endopeptidases/genética , Cisteína Endopeptidases/metabolismo , Evolução Molecular Direcionada/métodos , Vetores Genéticos/genética , Vetores Genéticos/metabolismo , Humanos , Marcação por Isótopo , Espectrometria de Massas , Modelos Moleculares , Dados de Sequência Molecular , Polipeptídeo Pancreático/genética , Polipeptídeo Pancreático/metabolismo , Peptídeos/química , Peptídeos/genética , Proteínas Recombinantes de Fusão/química , Proteínas Recombinantes de Fusão/genética , Tiorredoxinas/genética , Tiorredoxinas/metabolismo , Proteínas Virais/genética , Proteínas Virais/metabolismo
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