A Vector That Expresses Secreted Proteins on the Cell Surface
- 1 December 1989
- journal article
- research article
- Published by Mary Ann Liebert Inc in DNA
- Vol. 8 (10) , 753-758
- https://doi.org/10.1089/dna.1989.8.753
Abstract
A new vector, CDM8PI, has been constructed. It was derived from the plasmid expression vector CDM8, which has been used in the epitope-loss mutant isolation technique to map the epitopes on cell-surface proteins. The new vector allows the production of fusion proteins between normally secreted proteins and the membrane anchor moiety from a cell-surface protein, LFA-3, thereby expressing the fusion proteins on the cell surface. The vector extends the application of the epitope-loss mutant isolation technique to secreted proteins. The vector also allows the easy recovery of mutated proteins in unfused forms after the immunoselection and characterization.This publication has 12 references indexed in Scilit:
- Genetic analysis of monoclonal antibody and HIV binding sites on the human lymphocyte antigen CD4Cell, 1988
- Signal for Attachment of a Phospholipid Membrane Anchor in Decay Accelerating FactorScience, 1987
- Monoclonal antibody and ligand binding sites of the T cell erythrocyte receptor (CD2)Nature, 1987
- An LFA-3 cDNA encodes a phospholipid-linked membrane protein homologous to its receptor CD2Nature, 1987
- Cloning and sequencing of human cholesteryl ester transfer protein cDNANature, 1987
- Biochemistry of the glycosyl-phosphatidylinositol membrane protein anchorsBiochemical Journal, 1987
- Molecular cloning of the CD2 antigen, the T-cell erythrocyte receptor, by a rapid immunoselection procedure.Proceedings of the National Academy of Sciences, 1987
- The Lymphocyte Function Associated LFA-1, CD2, and LFA-3 Molecules: Cell Adhesion Receptors of the Immune SystemAnnual Review of Immunology, 1987
- High level transient expression of a chloramphenicol acetyl transferase gene by DEAE-dextran mediated DNA transfection coupled with a dimethyl sulfoxide or glycerol shock treatmentNucleic Acids Research, 1984
- Direct transfer of cloned genes from bacteria to mammalian cells.Proceedings of the National Academy of Sciences, 1980