Advances in the structural basis for angiotensin-1 converting enzyme (ACE) inhibitors

• Published in: Bioscience reports 2024-08, Vol.44 (8)
• Main Authors: Acharya, K Ravi, Gregory, Kyle S, Sturrock, Edward D
• Format: Article
• Language: English
• Subjects: Aldosterone; Allosteric properties; Amino acids; Angiotensin; Angiotensin-converting enzyme inhibitors; Angiotensin-Converting Enzyme Inhibitors - chemistry; Angiotensin-Converting Enzyme Inhibitors - pharmacology; Animals; Atherosclerosis; Binding sites; Biological effects; Blood pressure; Blood vessels; Cardiovascular disease; Cardiovascular diseases; Chloride; Computer applications; Cryoelectron Microscopy; Crystallography; Design; Dimerization; Drug development; Dynamic structural analysis; Effectiveness; Electrolyte balance; Electron microscopy; Enzymes; Enzymology; Humans; Hypertension; Inhibitors; Kidney diseases; Kinases; Metalloproteinase; Molecular Bases of Health & Disease; Molecular docking; Molecular Docking Simulation; Molecular dynamics; Molecular Dynamics Simulation; Molecular modelling; Peptides; Peptidyl-dipeptidase A; Peptidyl-Dipeptidase A - chemistry; Peptidyl-Dipeptidase A - metabolism; Pharmacology; Physiology; Protein Binding; Proteins; Renin; Renin-Angiotensin System - drug effects; Review; Sperm; Structural Biology; Structure-Activity Relationship
• ISSN: 0144-8463; 1573-4935; 1573-4935
• DOI: 10.1042/BSR20240130

Human somatic angiotensin-converting enzyme (ACE) is a key zinc metallopeptidase that plays a pivotal role in the renin-angiotensin-aldosterone system (RAAS) by regulating blood pressure and electrolyte balance. Inhibition of ACE is a cornerstone in the management of hypertension, cardiovascular diseases, and renal disorders. Recent advances in structural biology techniques have provided invaluable insights into the molecular mechanisms underlying ACE inhibition, facilitating the design and development of more effective therapeutic agents. This review focuses on the latest advancements in elucidating the structural basis for ACE inhibition. High-resolution crystallographic studies of minimally glycosylated individual domains of ACE have revealed intricate molecular details of the ACE catalytic N- and C-domains, and their detailed interactions with clinically relevant and newly designed domain-specific inhibitors. In addition, the recently elucidated structure of the glycosylated form of full-length ACE by cryo-electron microscopy (cryo-EM) has shed light on the mechanism of ACE dimerization and revealed continuous conformational changes which occur prior to ligand binding. In addition to these experimental techniques, computational approaches have also played a pivotal role in elucidating the structural basis for ACE inhibition. Molecular dynamics simulations and computational docking studies have provided atomic details of inhibitor binding kinetics and energetics, facilitating the rational design of novel ACE inhibitors with improved potency and selectivity. Furthermore, computational analysis of the motions observed by cryo-EM allowed the identification of allosteric binding sites on ACE. This affords new opportunities for the development of next-generation allosteric inhibitors with enhanced pharmacological properties. Overall, the insights highlighted in this review could enable the rational design of novel ACE inhibitors with improved efficacy and safety profiles, ultimately leading to better therapeutic outcomes for patients with hypertension and cardiovascular diseases.