Heterotrimeric G Proteins as Therapeutic Targets in Drug Discovery.
Animals
Asthma
/ drug therapy
Bacterial Toxins
/ administration & dosage
Drug Delivery Systems
/ methods
Drug Discovery
/ methods
Heart Failure
/ drug therapy
Heterotrimeric GTP-Binding Proteins
/ antagonists & inhibitors
Humans
Neoplasms
/ drug therapy
Peptides, Cyclic
/ administration & dosage
Protein Structure, Secondary
Receptors, G-Protein-Coupled
/ antagonists & inhibitors
Signal Transduction
/ drug effects
Thrombosis
/ drug therapy
Journal
Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531
Informations de publication
Date de publication:
28 05 2020
28 05 2020
Historique:
pubmed:
17
12
2019
medline:
24
10
2020
entrez:
17
12
2019
Statut:
ppublish
Résumé
Heterotrimeric G proteins are molecular switches in GPCR signaling pathways and regulate a plethora of physiological and pathological processes. GPCRs are efficient drug targets, and more than 30% of the drugs in use target them. However, selectively targeting an individual GPCR may be undesirable in various multifactorial diseases in which multiple receptors are involved. In addition, abnormal activation or expression of G proteins is frequently associated with diseases. Furthermore, G proteins harboring mutations often result in malignant diseases. Thus, targeting G proteins instead of GPCRs might provide alternative approaches for combating these diseases. In this review, we discuss the biochemistry of heterotrimeric G proteins, describe the G protein-associated diseases, and summarize the currently known modulators that can regulate the activities of G proteins. The outlook for targeting G proteins to treat diverse diseases is also included in this manuscript.
Identifiants
pubmed: 31841625
doi: 10.1021/acs.jmedchem.9b01452
doi:
Substances chimiques
Bacterial Toxins
0
Peptides, Cyclic
0
Receptors, G-Protein-Coupled
0
YM-254890
0
Heterotrimeric GTP-Binding Proteins
EC 3.6.5.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM