Identification of a small molecule that targets activator of G-protein signaling 8

Activator of G-protein signaling 8 (AGS8), also known as fibronectin type III domain containing 1 (FNDC1), is an accessory protein for heterotrimeric G-proteins involved in various cellular processes. The interaction between AGS8 and Gβγ subunit is a critical step in AGS8-mediated signaling, and a peptide that disrupts this interaction inhibited angiogenic events. To explore the broader potential of AGS8 biology, we investigated small molecules that block the AGS8-Gβγ interaction. Using a yeast-based system, in which cell growth depends on AGS8-mediated activation of G-protein pathway, we screened compounds from the RIKEN NPDepo library and identified one compound that effectively inhibited the formation of the AGS8-Gβγ complex. Consistent with the effects observed in AGS8 knockdown or peptide-treated cells, this compound attenuated VEGF-induced phosphorylation of signaling molecules and inhibited tube formation and migration of HUVECs. These data demonstrate the potential of the AGS8 inhibitor as a research tool and a therapeutic application.

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Publication Details

Journal
The Journal of Physiological Sciences
Published
2026-02-03
DOI
https://doi.org/10.1016/j.jphyss.2026.100064
Primary Topic
Protein Kinase Regulation and GTPase Signaling
Type
article
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article

Identification of a small molecule that targets activator of G-protein signaling 8

Takashi Iezaki, Motohiko Sato, Aya Yamamura, Hisaki Hayashi et al.
The Journal of Physiological Sciences
Protein Kinase Regulation and GTPase Signaling
article

Identification of a small molecule that targets activator of G-protein signaling 8

Takashi Iezaki, Motohiko Sato, Aya Yamamura, Hisaki Hayashi, Rie Takahashi, Alamgir Hossain, Hiroyuki Osada, Kazuo Umezawa, Hiroyuki Hirano
article en

Abstract

Activator of G-protein signaling 8 (AGS8), also known as fibronectin type III domain containing 1 (FNDC1), is an accessory protein for heterotrimeric G-proteins involved in various cellular processes. The interaction between AGS8 and Gβγ subunit is a critical step in AGS8-mediated signaling, and a peptide that disrupts this interaction inhibited angiogenic events. To explore the broader potential of AGS8 biology, we investigated small molecules that block the AGS8-Gβγ interaction. Using a yeast-based system, in which cell growth depends on AGS8-mediated activation of G-protein pathway, we screened compounds from the RIKEN NPDepo library and identified one compound that effectively inhibited the formation of the AGS8-Gβγ complex. Consistent with the effects observed in AGS8 knockdown or peptide-treated cells, this compound attenuated VEGF-induced phosphorylation of signaling molecules and inhibited tube formation and migration of HUVECs. These data demonstrate the potential of the AGS8 inhibitor as a research tool and a therapeutic application.

The Journal of Physiological SciencesVol. 76(1)
Aichi Medical University (JP), RIKEN Center for Sustainable Resource Science (JP)
Openalex Percentile: Top 69%
Protein Kinase Regulation and GTPase Signaling
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Identification of a small molecule that targets activator of G-protein signaling 8 — Takashi Iezaki, Motohiko Sato, et al. · The Journal of Physiological Sciences (2026) | TGRS Research Map | TGRS