Construction and mutagenesis of an anti-insulin single chain Fv (scFv) using protein engineering techniques: Identification of peptide mimotopes which inhibit scFv-insulin binding.
type: CreativeWork
description: Peptide mimotopes were found using random peptide library technology (Selectide technology) which bind to the paratope of an anti-insulin monoclonal antibody. These peptides inhibit insulin from binding to the anti-insulin antibody, indicating that they share at least part of the paratope for insulin. The 50% inhibitory concentrations (IC50) of certain peptides were determined to be less than one order of magnitude from that of insulin. The immunoglobulin variable region genes of the anti-insulin antibody were rescued and cloned independently as V(H) and V(k). A single chain Fv (scFv) was constructed using a polymerase chain reaction (PCR) assembly technique from the anti-insulin V(H) and V(k). The scFv demonstrated similar, but not identical binding properties to the parental anti-insulin antibody. Binding of four of six peptide mimotopes was localized to the variable region of the anti-insulin heavy chain. The heavy chain alone was also able to bind insulin. None of the peptides bound to the variable region of the kappa light chain. Mutagenesis studies indicated that complementarity determining region (CDR) 1 and CDR3 of the heavy chain were important for binding to insulin and to the peptides. Position 99 in CDR3 of the heavy chain was found to be most critical for binding to insulin. Mutational analysis of position 99 revealed that glycine and alanine are acceptable residues for position 99, whereas valine and threonine are not. This finding suggested that residue size, not hydrophobicity determined whether the antibody could bind to insulin.
abstract: Peptide mimotopes were found using random peptide library technology (Selectide technology) which bind to the paratope of an anti-insulin monoclonal antibody. These peptides inhibit insulin from binding to the anti-insulin antibody, indicating that they share at least part of the paratope for insulin. The 50% inhibitory concentrations (IC50) of certain peptides were determined to be less than one order of magnitude from that of insulin. The immunoglobulin variable region genes of the anti-insulin antibody were rescued and cloned independently as V(H) and V(k). A single chain Fv (scFv) was constructed using a polymerase chain reaction (PCR) assembly technique from the anti-insulin V(H) and V(k). The scFv demonstrated similar, but not identical binding properties to the parental anti-insulin antibody. Binding of four of six peptide mimotopes was localized to the variable region of the anti-insulin heavy chain. The heavy chain alone was also able to bind insulin. None of the peptides bound to the variable region of the kappa light chain. Mutagenesis studies indicated that complementarity determining region (CDR) 1 and CDR3 of the heavy chain were important for binding to insulin and to the peptides. Position 99 in CDR3 of the heavy chain was found to be most critical for binding to insulin. Mutational analysis of position 99 revealed that glycine and alanine are acceptable residues for position 99, whereas valine and threonine are not. This finding suggested that residue size, not hydrophobicity determined whether the antibody could bind to insulin.
author: Lake, Douglas Fletcher.
language: en
keywords: Dissertations, Academic., Molecular biology., Immunology.
date published: 1993
date modified: 2026-07-24T00:57:22Z
provider: University of Arizona
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: The University of Arizona.

PropertyValue
property ID: Handle
value: http://hdl.handle.net/10150/186310