Introduction
Figure 1: GLPR from pymol
History
The discovery, clinical development, and characterization of glucagon-like-peptide-1 (GLP-1) encompasses more than 30 years of research from many different scientists/investigators. GLP-1 alongside gastric inhibitory peptide (GIP) are the two primary incretin hormones released by pancreatic beta cells of the intestines following the ingestion of glucose.
Function
GLP-1 plays various critical roles in biological processes throughout the body. In adipose tissues, GLP-1 facilitates fat deposition. In bone, GLP-1 inhibits bone absorption. In the brain, both GLP-1 and GIP are involved in memory formation as well as the control of appetite.
Within the pancreas, GLP-1 promotes beta cell proliferation and inhibit apoptosis, allowing for clinically-desirable insulinotropic effects.
GLP-1 exerts its effects by binding to the GLP-1 receptor (GLP-1R) which stimulate effects in the body via G-protein coupled signaling. Receptor binding activates and increases the level of intracellular cyclic monophosphate (cAMP) in pancreatic beta cells as well as glucose-dependent insulin secretion.
Relevance
Marketed GLP-1R agonists such as dulaglutide, exenatide, liraglutide, and semaglutide represent an expanding drug class with beneficial therapeutic effects for those suffering from type II diabetes and obesity. In more recent years, co-agonist drugs which stimulate both the GLP-1R and GIPR pathways have been synthesized. These co-agonist drugs provide serious promise with regards to assisting those affected by the aforementioned conditions. The co-agonist drug, Tirzepatide, is regarded as one of the most promising candidates for better treatment of obesity and type II diabetes by improving weight reduction and glycemic control.
In this review page, we present the signaling pathways as well as structural highlights within the GLP-1 GPCR pathway in the pancreatic beta cell, focusing on its relevance with regards to the therapeutic effects of the Tirzepatide drug.
Structure
Extracellular Domain
Broadly the extracellular reactions between GLP-1 and GLP-1R lie between residues 15-32 on the peptide GLP-1. Residues L32, F28, W31 of the peptide and L36 and W214 of the receptor all utilize hydrophobic interactions or van der waals for affinity and binding, but exclusively F28, W31, and W214 have pi stackin which future maximizes interactions to increase binding. Furthermore, there is a strong hydrogen bond between D15 of the peptide to the R380 receptor. Van der Waals interactions continue on the residues Y19, L20, and V16 on the peptide as they interact with L141 and L210 of the receptor. Another hydrogen bond between E27 and Q21 also occurs. Finally, there is a patch of extensive hydrogen bonding in an almost chainlike fashion goin from L32 of the receptor to E21 of the peptide, to R299 of the receptor, to the S17 of the peptide which then interacts with Y205 and T298 both of the receptor.
Active Site/Binding Site
The transmembrane core is key to the active site/binding site. One of the main interactions between GLP-1 and GLP-1R includes the hydrogen bond between H7 and Q234 as the N-terminus of the peptide is bound to the transmembrane domain of the receptor. This interaction provides the most stability within the structure. It is further enhanced by hydrophobic interactions between residues V16 and F12 of the peptide and L384 and L141 of the receptor. Notably there is a hydrogen bond T13 of the peptide and K197 of the receptor.
Applications
Tirzepatide
The co-agonist drug, Tirzepatide, is regarded as one of the most promising candidates for better treatment of obesity and type II diabetes by improving weight reduction and glycemic control. Tirzepatide is a dual agonist of the glucagon-like-peptide-1 receptor (GLP-1R) and the glucose-dependent insulinotropic polypeptide receptor (GIPR). Co-agonism of both GLP-1 and GIP pathways provides beneficial therapeutic effects by mimicking desirable components of each respective pathway. Tirzepatide exhibits similar pharmacology to the native GIP pathway, but differs with regards to the GLP-1 pathway, as it shows biased signaling of cAMP. This biased signaling, also called differential signaling, allows for the co-agonist drug to increase efficacy in glucose control and body weight regulation for treating type II diabetes as well as obesity.
Implications
Future Directions
