Degradation of lipid droplets by chimeric autophagy-tethering compounds

• Published in: Cell research Vol. 31; no. 9; pp. 965 - 979
• Main Authors: Fu, Yuhua, Chen, Ningxie, Wang, Ziying, Luo, Shouqing, Ding, Yu, Lu, Boxun
• Format: Journal Article
• Language: English
• Published: Singapore Springer Singapore 01.09.2021; Nature Publishing Group
• Subjects: 101/58; 13/106; 13/109; 14/19; 14/34; 631/337; 631/80/39/2346; 64/60; 82/29; 82/83; 96/1; 96/95; Animal models; Animals; Autophagosomes - metabolism; Autophagy; Binding; Biomedical and Life Sciences; Biomolecules; Cell Biology; Cellular structure; Chimera - metabolism; Chimeras; Degradation; Droplets; Life Sciences; Lipid Droplets - metabolism; Lipid Metabolism; Lipids; Mice; Phagocytosis; Phenotypes; Proteins; Proteins - metabolism; Proteolysis; Tethering
• ISSN: 1001-0602; 1748-7838; 1748-7838
• DOI: 10.1038/s41422-021-00532-7

Degrading pathogenic proteins by degrader technologies such as PROTACs (proteolysis-targeting chimeras) provides promising therapeutic strategies, but selective degradation of non-protein pathogenic biomolecules has been challenging. Here, we demonstrate a novel strategy to degrade non-protein biomolecules by autophagy-tethering compounds (ATTECs), using lipid droplets (LDs) as an exemplar target. LDs are ubiquitous cellular structures storing lipids and could be degraded by autophagy. We hypothesized that compounds interacting with both the LDs and the key autophagosome protein LC3 may enhance autophagic degradation of LDs. We designed and synthesized such compounds by connecting LC3-binding molecules to LD-binding probes via a linker. These compounds were capable of clearing LDs almost completely and rescued LD-related phenotypes in cells and in two independent mouse models with hepatic lipidosis. We further confirmed that the mechanism of action of these compounds was mediated through LC3 and autophagic degradation. Our proof-of-concept study demonstrates the capability of degrading LDs by ATTECs. Conceptually, this strategy could be applied to other protein and non-protein targets.