Identification of NUV-244 as a PNPLA3 I148M degrading small molecule

The PNPLA3 I148M variant is a key genetic determinant of metabolic dysfunction-associated steatotic liver disease (MASLD) and related conditions, contributing to lipid metabolism dysregulation and disease progression. To identify small molecules that modulate PNPLA3 I148M, we conducted a high-content screen of over 820,000 compounds and identified NUV-244, a potent degrader of PNPLA3 I148M in liver-derived cells. NUV-244 reduces PNPLA3 I148M levels on lipid droplets via the ubiquitin-proteasome system, involving the E3 ligase BFAR, without affecting PNPLA2. It restores lipid droplet morphology and improves cellular fitness in PNPLA3 I148M-expressing cells. These findings provide a tool to investigate PNPLA3 I148M function and offer a potential strategy for developing targeted therapies for MASLD and related diseases. By enabling selective degradation of PNPLA3 I148M, this approach expands therapeutic possibilities beyond genetic manipulation, addressing a critical need in metabolic liver disease research.

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Publication Details

Journal
iScience
Published
2025-04-08
DOI
https://doi.org/10.1016/j.isci.2025.112384
Citations
2
Primary Topic
Electron Spin Resonance Studies
Type
article
Field-Weighted Citation Impact
3.27
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article

Identification of NUV-244 as a PNPLA3 I148M degrading small molecule

Benjamin Bader, Nina Zablowsky, Ralf Lesche, Zuzanna Makowska et al.
2 citations
iScience
Electron Spin Resonance Studies
3.27
article

Identification of NUV-244 as a PNPLA3 I148M degrading small molecule

Benjamin Bader, Nina Zablowsky, Ralf Lesche, Zuzanna Makowska, Lisa Bedford, Stefano Romeo, Katrin Juenemann, Stephan Fasler, Vera Puetter, Franz von Nussbaum, Nico Braeuer, H. Steuber, Patrick Steigemann, Mary Helen Black, Jonathan S. Packer, Filippos Klironomos, David Schaller, Sabine Schwarz, Martin Lange, Frederick E. Dewey, Daniela Launhardt, Nicole Dittmar
article en
2 citations

Abstract

The PNPLA3 I148M variant is a key genetic determinant of metabolic dysfunction-associated steatotic liver disease (MASLD) and related conditions, contributing to lipid metabolism dysregulation and disease progression. To identify small molecules that modulate PNPLA3 I148M, we conducted a high-content screen of over 820,000 compounds and identified NUV-244, a potent degrader of PNPLA3 I148M in liver-derived cells. NUV-244 reduces PNPLA3 I148M levels on lipid droplets via the ubiquitin-proteasome system, involving the E3 ligase BFAR, without affecting PNPLA2. It restores lipid droplet morphology and improves cellular fitness in PNPLA3 I148M-expressing cells. These findings provide a tool to investigate PNPLA3 I148M function and offer a potential strategy for developing targeted therapies for MASLD and related diseases. By enabling selective degradation of PNPLA3 I148M, this approach expands therapeutic possibilities beyond genetic manipulation, addressing a critical need in metabolic liver disease research.

iScienceVol. 28(5)
Foresite (United States) (US), Nuvisan (Germany) (DE), University of Gothenburg (SE)
Openalex Percentile: Top 9%
Electron Spin Resonance Studies
3.27
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