Skip to main content
Log in

An Improved Rapid Method for Selecting Monoclonal Antibodies with High Catalytic Activities

  • Published:
Journal of Protein Chemistry Aims and scope Submit manuscript

Abstract

Monoclonal antibodies were raised against a β-naphthyl phosphonate hapten (1) to elicit antibodies capable of catalyzing the hydrolysis of β-naphthyl acetate (3). After cell fusion, potential catalytic antibody-producing hybridomas were selected, by use of a competitive inhibition assay on the basis of the binding activity for a short transition-state analogue (inhibitor 5), followed by use of high-performance liquid chromatography analysis for the hybridoma supernatants to screen the antibodies processing catalytic activities. It was shown that supernatants of 12 wells had high binding activity with inhibitor and of them, 7 had catalytic activities. After cloning by limiting dilution, we got two hybridoma clones producing monoclonal antibodies which catalyzed the hydrolysis of β-naphthyl acetate. This combination of competitive inhibition assay with high-performance liquid chromatography analysis represents an improved rapid approach for the screening of potential catalytic antibodies and significantly increases the possibility of obtaining efficient catalytic monoclonal antibodies. Further study of the catalytic antibodies revealed significant rate enhancement (K cat/K uncat ∼ 106) and specificity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yuan, Y.R., Yang, B.H. & Ji, Y.Y. An Improved Rapid Method for Selecting Monoclonal Antibodies with High Catalytic Activities. J Protein Chem 16, 733–738 (1997). https://doi.org/10.1023/A:1026355614913

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1026355614913

Navigation