Multi-chain eukaryotic display vectors and uses thereof
View Patent ↗A eukaryotic expression vector capable of displaying a multi-chain polypeptide on the surface of a host cell is provided, such that the biological activity of the multi-chain polypeptide is exhibited at the surface of the host cell. Such a vector allows for the display of complex biologically active polypeptides, e.g., biologically active multi-chain polypeptides such as immunoglobulin Fab fragments. The present invention describes and enables the successful display of a multi-chain polypeptide on the surface of a eukaryotic host cell. Preferred vectors are described for expressing the chains of a multi-chain polypeptide in a host cell separately and independently (e.g., under separate vector control elements, and/or on separate expression vectors, thus forming a matched vector set). The use of such matched vector sets provides flexibility and versatility in the generation of eukaryotic display libraries, for example the ability to generate and to display multi-chain polypeptides by combining and recombining vectors that express variegations of the individual chains of a multi-chain polypeptide. Entire repertoires of novel chain combinations can be devised using such vector sets.
1. A method for screening a library of human antibodies in yeast, comprising:
creating a library of antibodies in yeast cells, wherein the step of creating the library comprises: (i) mutagenizing pre-selected V H and V L to produce a multiplicity of variegated V H and V L , and (ii) transferring the multiplicity of variegated V H and V L into expression vectors by homologous recombination;
expressing the library of human antibodies in yeast cells, wherein each of the human antibodies comprises a V H and a V L , which form an assembled V H /V L multi-chain polypeptide;
interacting a target protein with the library of human antibodies; and
selecting those human antibodies based on their binding to the target protein.
2. The method of claim 1 , wherein the V H and V L each is linked with a leucine zipper domain by which the V H and V L are associated with each other to form the V H /V L multi-chain polypeptide.
3. The method of claim 2 , wherein the leucine zipper domains linked to the V H and V L are leucine zipper domains from Fos and Jun.