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STRATEGIES AND TOOLS TO DEVELOP A BETTER GPCR-TARGETED THERAPEUTIC

By Lisa Minor, Ph.D.

G-Protein Coupled Receptors (GPCRs) are one of the most pharmacologically successful drug targets. 35% of all drugs target this protein superfamily1. GPCR-targeted therapeutics continues to be successful and in fact, 19% of newly approved drugs target GPCRs2.

The early generation of small molecule drugs targeted either orthosteric agonist or antagonist activity of these receptors’ G-protein cell signaling pathway. In recent years, we have discovered more about GPCRs including crystal structures, improvements in computer-aided rational drug design, differences in the cell signaling pathways and as well as how these receptors dimerize.

Targeting Cell Signaling Bias: The increase in understanding of GPCR signaling pharmacology comes about in part from better and more sensitive screening assays. From these tools we have learned that GPCRs are much more complicated than had been believed

and hence much more interesting and potentially more valuable as drug discovery targets. Evidence shows that GPCRs signal through beta-arrestin in addition to G-proteins and that ligands can trigger biased cell signaling in one direction or the other3.
This can have a therapeutic advantage such as the case of TRV-120023 in a heart failure indication. This selective molecule against the Angiotensin-1 receptor (AT1R) can not only reduce blood pressure but also positively affect heart failure. Other ARBs (angiotensin receptor blockers) did not show this effect. Why? The reason appears that TRV-120023 can block the effect of endogenous Angiotensin II while promoting cardiac contractility. Unlike its competitor ARB, Losartin, TRV-120023 activates MAPK and AKT signaling through the beta-arrestin cell signaling pathway4. This type of signaling bias has obvious therapeutic ramifications.

As a result, it appears that an important strategy would be to identify molecules that have selective patterns of cell signaling to see how they affect the desired pharmacology. This has the advantage of providing a molecule that may be efficacious toward the disease with reduced side effects due to the alternate signaling pathways.

Targeting Allosteric Modulation: An additional strategy is to identify allosteric modulators of GPCR’s3, 5. Positive allosteric molecules have an advantage that they only work in the presence of the native ligand thus amplifying the ligand’s effect while having no activity on its own.

Demonstration of potential therapeutic benefits of allosteric modulation and liabilities of screening strategies is seen with mGLUR56. In this case, allosteric modulators of mGLUR5 were identified using a cell line transfected with an abundant amount of mGLUR5 receptors. These compounds were shown to have a liability of causing seizures in animals. However, when retested in a lower expressing cell line and native cells, it was possible to differentiate compounds that were allosteric agonists from those that were positive allosteric modulators. The allosteric modulators no longer demonstrated seizure liability while the effectiveness against the targeted therapeutic indication, schizophrenia remained. Negative allosteric modulators are also relevant against receptors that have native constitutive activity.

A critical necessity for taking advantage of the multiple cell signaling paradigms of GPCR’s is to have the ability to measure them in robust functional assays in cells with the correct receptor expression and across appropriate orthologs to detect selectivity.

How do we help? A robust functional cell-based assay platform for the majority of GPCRs exists at Multispan. We have the capacity to measure and evaluate cell signaling bias as well as to test for positive and negative allosteric modulation. We have also retained the ability to measure traditional GPCR features such as ligand-receptor binding and GTPS assay. We leverage our expertise by providing off-the-shelf products such as stable cell lines with validated assays, custom cell line generation with specific receptor expression profiles and assay development with the target of your choosing.

Next, our screening services can help you jump start your program working as your assay development and screening team. With our help, we can move your programs rapidly from hit identification to hit-to-lead. Moreover, we can continue working with you to optimize your compounds through SAR lead optimization. Our SAR primary screen offers unparalleled next-day turnaround. We also support secondary and tertiary screens in orthologs/paralogs GPCRs, primary cells and GPCR safety liability panels specifically designed for your program.

We have achieved a 100% return customer rate over our last decade in business and pride ourselves on excellence. Let us be your GPCR drug discovery arm.

References:

  1. Sriram Kand Insel A, GPCRs as targets for approved drugs: How many targets and how many drugs? Molecular pharmacology Jan 3, 2018, mol.117.111062; DOI: https://doi.org/10.1124/mol.117.111062
  2. Khoury E et al, Allosteric and biased g protein-coupled receptor signaling regulation: potentials for new therapeutics. Front Endocrinol (Lausanne).

2014 May 8;5:68. doi: 10.3389/fendo.2014.00068. eCollection 2014.

  1. Kim KS et al, β-Arrestin-biased AT1R stimulation promotes cell survival during acute cardiac injury. 2012 Oct 15;303(8): H1001-10. doi: 10.1152/

ajpheart.00475.2012. Epub 2012 Aug 10.

  1. Wootten D et al, Emerging paradigms in GPCR allostery: implications for drug discovery, Nat Rev Drug Discov. 2013 Aug;12(8):630-44. doi: 10.1038/

nrd4052.

  1. Rook JM et al, Unique signaling profiles of positive allosteric modulators of metabotropic glutamate receptor subtype 5 determine differences in in

vivo activity. Biol Psychiatry. 2013 Mar 15;73(6):501-9. doi: 10.1016/j.biopsych.2012.09.012. Epub 2012 Nov 7

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