Standing out in the field of IgY Immunotechnology

  • Home
    Home A full collection of all the Research Archive entries.
  • Years
    Years Sort entries by year.
  • Tags
    Tags Displays a list of tags that have been used in the blog.
  • Archives
    Archives Contains a list of research entries that were created previously.

Development of an efficient signal amplification strategy for label-free enzyme immunoassay using two site-specific biotinylated recombinant proteins.

Posted by on in 2015
  • Font size: Larger Smaller
  • Hits: 973
  • Print
  • Tang JB1Tang Y2Yang HM3. 2015. Anal Chim Acta. 859:66-71. doi: 10.1016/j.aca.2014.12.020. Epub 2014 Dec 12.
  • 1School of Pharmacy, Weifang Medical University, Weifang 261053, PR China.
  • 2Affiliated Hospital of Weifang Medical University, Weifang 261041, PR China.
  • 3School of Pharmacy, Weifang Medical University, Weifang 261053, PR China. Electronic address: yanghongming2006@sohu.com.

Abstract

Constructing a recombinant protein between a reporter enzyme and a detector protein to produce a homogeneous immunological reagent is advantageous over random chemical conjugation. However, the approach hardly recombines multiple enzymes in a difunctional fusion protein, which results in insufficient amplification of the enzymatic signal, thereby limiting its application in further enhancement of analytical signal. In this study, two site-specific biotinylated recombinant proteins, namely, divalent biotinylated alkaline phosphatase (AP) and monovalent biotinylated ZZ domain, were produced by employing the Avitag-BirA system. Through the high streptavidin (SA)-biotin interaction, the divalent biotinylated APs were clustered in the SA-biotin complex and then incorporated with the biotinylated ZZ. This incorporation results in the formation of a functional macromolecule that involves numerous APs, thereby enhancing the enzymatic signal, and in the production of several ZZ molecules for the interaction with immunoglobulin G (IgG) antibody. The advantage of this signal amplification strategy is demonstrated through ELISA, in which the analytical signal was substantially enhanced, with a 32-fold increase in the detection sensitivity compared with the ZZ-AP fusion protein approach. The proposed immunoassay without chemical modification can be an alternative strategy to enhance the analytical signals in various applications involving immunosensors and diagnostic chips, given that the label-free IgG antibody is suitable for the ZZ protein.

Copyright © 2014 Elsevier B.V. All rights reserved.

KEYWORDS:

Alkaline phosphatase; Enzyme immunoassay; Label-free; Signal amplification; Site-specific enzymatic biotinylation; ZZ domain

PMID:
 
25622607
 
[PubMed - indexed for MEDLINE]
Last modified on