Regulation of Peptidase Activity beyond the Active Site in Human Health and Disease

Int J Mol Sci. 2023 Dec 4;24(23):17120. doi: 10.3390/ijms242317120.

Abstract

This comprehensive review addresses the intricate and multifaceted regulation of peptidase activity in human health and disease, providing a comprehensive investigation that extends well beyond the boundaries of the active site. Our review focuses on multiple mechanisms and highlights the important role of exosites, allosteric sites, and processes involved in zymogen activation. These mechanisms play a central role in shaping the complex world of peptidase function and are promising potential targets for the development of innovative drugs and therapeutic interventions. The review also briefly discusses the influence of glycosaminoglycans and non-inhibitory binding proteins on enzyme activities. Understanding their role may be a crucial factor in the development of therapeutic strategies. By elucidating the intricate web of regulatory mechanisms that control peptidase activity, this review deepens our understanding in this field and provides a roadmap for various strategies to influence and modulate peptidase activity.

Keywords: allostery; exosite; glycosaminoglycan; inhibition; interaction; protease.

Publication types

  • Review

MeSH terms

  • Allosteric Regulation
  • Allosteric Site
  • Binding Sites
  • Catalytic Domain
  • Glycosaminoglycans*
  • Humans
  • Peptide Hydrolases*
  • Proteolysis

Substances

  • Glycosaminoglycans
  • Peptide Hydrolases