Selective inhibition of matrix metalloproteinase 10 (MMP10) with a single-domain antibody

J Biol Chem. 2020 Feb 21;295(8):2464-2472. doi: 10.1074/jbc.RA119.011712. Epub 2020 Jan 17.

Abstract

Since their discovery, the matrix metalloproteinase (MMP) family proteases have been considered as therapeutic targets in numerous diseases and disorders. Unfortunately, clinical trials with MMP inhibitors have failed to yield any clinical benefits of these inhibitors. These failures were largely due to a lack of MMP-selective agents; accordingly, it has become important to identify a platform with which high selectivity can be achieved. To this end, we propose using MMP-targeting antibodies that can achieve high specificity in interactions with their targets. Using a scaffold of single-domain antibodies, here we raised a panel of MMP10-selective antibodies through immunization of llamas, a member of the camelid family, whose members generate conventional heavy/light-chain antibodies and also smaller antibodies lacking light-chain and CH1 domains. We report the generation of a highly selective and tightly binding MMP10 inhibitor (Ki < 2 nm). Using bio-layer interferometry-based binding assays, we found that this antibody interacts with the MMP10 active site. Activity assays demonstrated that the antibody selectively inhibits MMP10 over its closest relative, MMP3. The ability of a single-domain antibody to discriminate between the most conserved MMP pair via an active site-directed mechanism of inhibition reported here supports the potential of this antibody as a broadly applicable scaffold for the development of selective, tightly binding MMP inhibitors.

Keywords: MMP10; MMP3; antibody; antibody engineering; antibody selectivity; camelid; matrix metalloproteinase; metalloprotease; nanobody; orthosteric inhibitor; protease; protease inhibitor; sdAb; single-domain antibody.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Camelids, New World
  • Humans
  • Immunization
  • Kinetics
  • Matrix Metalloproteinase 10 / metabolism*
  • Matrix Metalloproteinase Inhibitors / pharmacology*
  • Peptide Library
  • Recombinant Proteins / metabolism
  • Saccharomyces cerevisiae / metabolism
  • Single-Domain Antibodies / pharmacology*
  • Substrate Specificity / drug effects
  • alpha 1-Antitrypsin / metabolism

Substances

  • Matrix Metalloproteinase Inhibitors
  • Peptide Library
  • Recombinant Proteins
  • Single-Domain Antibodies
  • alpha 1-Antitrypsin
  • Matrix Metalloproteinase 10