An Enzyme-Linked Immunosorbent Assay (ELISA) for Quantification of Circulating Pi*Z Alpha1-Antitrypsin Polymers

Methods Mol Biol. 2024:2750:113-122. doi: 10.1007/978-1-0716-3605-3_11.

Abstract

Enzyme-linked immunosorbent assay (ELISA) is a sensitive immunoassay based on specific antigen-antibody reaction that is used for quantitative/qualitative analysis of various analytes in serum, plasma, saliva, cell and tissue lysates, and urine. ELISAs are typically performed in multi-well plates and depending on the design require coating antibody/antigen, analyte, detection antibodies, buffer, wash solution, and substrate/chromogen. Here we describe highly specific monoclonal antibody-based ELISA that detects circulating polymers formed by Pi*Z variant of human alpha-1-antitrypsin (Z-AAT). The circulating Z-AAT polymers are present in all individuals with inherited Pi*Z AAT deficiency. Thus, our assay provides a useful tool to examine the clinical significance and utility of Z-AAT polymers.

Keywords: ELISA; Monoclonal antibody; Quantification; Substrate; Z-AAT polymers.

MeSH terms

  • Antibodies, Monoclonal*
  • Biological Assay
  • Body Fluids*
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Polymers

Substances

  • Antibodies, Monoclonal
  • Polymers