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G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity.
- Source :
-
Scientific reports [Sci Rep] 2017 Mar 07; Vol. 7, pp. 43480. Date of Electronic Publication: 2017 Mar 07. - Publication Year :
- 2017
-
Abstract
- The recognition specificity of monoclonal antibodies (mAbs) has made mAbs among the most frequently used tools in both basic science research and in clinical diagnosis and therapies. Precise determination of the epitope allows the development of epitope tag systems to be used with recombinant proteins for various purposes. Here we describe a new family of tag derived from the epitope recognized by a highly specific mAb G196. The minimal epitope was identified as the five amino acid sequence Asp-Leu-Val-Pro-Arg. Permutation analysis was used to characterize the binding requirements of mAb G196, and the variable regions of the mAb G196 were identified and structurally analyzed by X-ray crystallography. Isothermal titration calorimetry revealed the high affinity (K <subscript>d</subscript>  = 1.25 nM) of the mAb G196/G196-epitope peptide interaction, and G196-tag was used to detect several recombinant cytosolic and nuclear proteins in human and yeast cells. mAb G196 is valuable for developing a new peptide tagging system for cell biology and biochemistry research.
- Subjects :
- Amino Acid Sequence
Animals
Antibodies, Monoclonal biosynthesis
Antibodies, Monoclonal isolation & purification
Antibody Affinity
Antibody Specificity
Binding Sites
Cloning, Molecular
Crystallography, X-Ray
Epitopes genetics
Epitopes immunology
Escherichia coli genetics
Escherichia coli metabolism
Gene Expression
Genetic Vectors chemistry
Genetic Vectors metabolism
HeLa Cells
Humans
Mice
Peptides genetics
Peptides immunology
Protein Binding
Protein Conformation, alpha-Helical
Protein Conformation, beta-Strand
Protein Interaction Domains and Motifs
Recombinant Proteins chemistry
Recombinant Proteins genetics
Recombinant Proteins immunology
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae metabolism
Antibodies, Monoclonal chemistry
Epitope Mapping methods
Epitopes chemistry
Peptides chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 7
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 28266535
- Full Text :
- https://doi.org/10.1038/srep43480