Title: | Yeast surface display for screening combinatorial polypeptide libraries |
Address: | "Department of Chemical Engineering, University of Illinois, Urbana 61801, USA" |
ISSN/ISBN: | 1087-0156 (Print) 1087-0156 (Linking) |
Abstract: | "Display on the yeast cell wall is well suited for engineering mammalian cell-surface and secreted proteins (e.g., antibodies, receptors, cytokines) that require endoplasmic reticulum-specific post-translational processing for efficient folding and activity. C-terminal fusion to the Aga2p mating adhesion receptor of Saccharomyces cerevisiae has been used for the selection of scFv antibody fragments with threefold decreased antigen dissociation rate from a randomly mutated library. A eukaryotic host should alleviate expression biases present in bacterially propagated combinatorial libraries. Quantitative flow cytometric analysis enables fine discrimination of kinetic parameters for protein binding to soluble ligands" |
Keywords: | "Animals Cloning, Molecular Endoplasmic Reticulum/metabolism Escherichia coli Flow Cytometry Gene Expression Genomic Library Immunoglobulin Fragments/*biosynthesis/chemistry Kinetics Mammals Mating Factor Membrane Fusion Mutagenesis *Peptide Biosynthesis *;" |
Notes: | "MedlineBoder, E T Wittrup, K D eng Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. 1997/06/01 Nat Biotechnol. 1997 Jun; 15(6):553-7. doi: 10.1038/nbt0697-553" |