Literature DB >> 24943310

1D4: a versatile epitope tag for the purification and characterization of expressed membrane and soluble proteins.

Laurie L Molday1, Robert S Molday.   

Abstract

Incorporation of short epitope tags into proteins for recognition by commercially available monoclonal or polyclonal antibodies has greatly facilitated the detection, characterization, localization, and purification of heterologously expressed proteins for structure-function studies. A number of tags have been developed, but many epitope-antibody combinations do not work effectively for all immunochemical techniques due to the nature of the tag and the specificity of the antibodies. A highly versatile, multipurpose epitope tag is the 9 amino acid C-terminal 1D4 peptide. This peptide tag together with the Rho1D4 monoclonal antibody can be used to detect proteins in complex mixtures by western blotting and ELISA assays, localize proteins in cells by immunofluorescence and immunoelectron microscopic labeling techniques, identify subunits and interacting proteins by co-immunoprecipitation, and purify functionally active proteins including membrane proteins by immunoaffinity chromatography. In this chapter we describe various immunochemical procedures which can be used for the detection, purification and localization of 1D4-tagged proteins for structure-function studies.

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Year:  2014        PMID: 24943310      PMCID: PMC4227631          DOI: 10.1007/978-1-4939-1034-2_1

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  22 in total

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Journal:  Anal Biochem       Date:  2005-11-02       Impact factor: 3.365

4.  The synthesis and high-level expression of a beta2-adrenergic receptor gene in a tetracycline-inducible stable mammalian cell line.

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Journal:  Protein Sci       Date:  2006-06       Impact factor: 6.725

5.  Expression of a synthetic bovine rhodopsin gene in monkey kidney cells.

Authors:  D D Oprian; R S Molday; R J Kaufman; H G Khorana
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

6.  Inhibition of monoclonal antibody binding and proteolysis by light-induced phosphorylation of rhodopsin.

Authors:  R S Molday; D MacKenzie
Journal:  Biochemistry       Date:  1985-01-29       Impact factor: 3.162

7.  Localization of binding sites for carboxyl terminal specific anti-rhodopsin monoclonal antibodies using synthetic peptides.

Authors:  D MacKenzie; A Arendt; P Hargrave; J H McDowell; R S Molday
Journal:  Biochemistry       Date:  1984-12-18       Impact factor: 3.162

8.  Antigen-antibody interaction. Synthetic peptides define linear antigenic determinants recognized by monoclonal antibodies directed to the cytoplasmic carboxyl terminus of rhodopsin.

Authors:  R S Hodges; R J Heaton; J M Parker; L Molday; R S Molday
Journal:  J Biol Chem       Date:  1988-08-25       Impact factor: 5.157

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Journal:  Invest Ophthalmol Vis Sci       Date:  1987-01       Impact factor: 4.799

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Authors:  Faraz Quazi; Stepan Lenevich; Robert S Molday
Journal:  Nat Commun       Date:  2012-06-26       Impact factor: 14.919

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6.  Application of Strep-Tactin XT for affinity purification of Twin-Strep-tagged CB2, a G protein-coupled cannabinoid receptor.

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